SRX12666031 CL100066959_L01_535 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618182 RB1108 CL100066959_L01_535 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666032 CL100065780_L02_read_16 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618183 M481 CL100065780_L02_read_16 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666033 CL100065711_L01_read_3 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618184 M782 CL100065711_L01_read_3 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666034 CL100066959_L01_536 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618185 RB1118 CL100066959_L01_536 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666035 CL100066959_L01_537 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618186 RB1151 CL100066959_L01_537 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666036 CL100066959_L01_538 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618187 RB1155 CL100066959_L01_538 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666037 CL100066959_L01_539 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618188 RB1168 CL100066959_L01_539 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666038 CL100066959_L02_541 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618189 RB1184 CL100066959_L02_541 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666039 CL100065783_L01_read_2 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618190 M633 CL100065783_L01_read_2 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666040 CL100067047_L01_563 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618191 M39 CL100067047_L01_563 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666041 CL100067047_L01_564 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618192 M41 CL100067047_L01_564 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666042 CL100067047_L02_565 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618193 M42 CL100067047_L02_565 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666043 CL100067047_L02_566 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618194 M64 CL100067047_L02_566 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666044 CL100067047_L02_568 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618195 M125 CL100067047_L02_568 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666045 CL100067047_L02_570 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618196 M128 CL100067047_L02_570 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666046 CL100067047_L02_571 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618197 M129 CL100067047_L02_571 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666047 CL100067040_L01_573 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618198 M133 CL100067040_L01_573 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666048 CL100067040_L01_574 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618199 M289 CL100067040_L01_574 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666049 CL100067040_L01_579 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618200 E116 CL100067040_L01_579 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666050 CL100065783_L01_read_3 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618201 M634 CL100065783_L01_read_3 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666051 CL100067040_L01_580 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618202 E118 CL100067040_L01_580 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666052 CL100067041_L01_594 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618203 E119 CL100067041_L01_594 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666053 CL100067041_L01_595 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618204 E120 CL100067041_L01_595 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666054 CL100081630_L01_508 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618205 M1145 CL100081630_L01_508 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666055 CL100066959_L02_542 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618206 RB1194 CL100066959_L02_542 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666056 CL100066959_L02_543 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618207 RB1195 CL100066959_L02_543 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666057 CL100066959_L02_545 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618208 RB1202 CL100066959_L02_545 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666058 CL100066959_L02_546 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618209 RB1205 CL100066959_L02_546 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666059 CL100066959_L02_547 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618210 RB1207 CL100066959_L02_547 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666060 CL100065711_L01_read_5 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618211 M854 CL100065711_L01_read_5 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666061 CL100066959_L02_548 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618212 RB1209 CL100066959_L02_548 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666062 CL100066961_L01_549 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618213 RB1211 CL100066961_L01_549 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666063 CL100066961_L01_550 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618214 RB1213 CL100066961_L01_550 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666064 CL100066961_L01_551 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618215 RB1219 CL100066961_L01_551 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666065 CL100066961_L01_552 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618216 RB1220 CL100066961_L01_552 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666066 CL100066961_L01_553 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618217 RB1221 CL100066961_L01_553 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666067 CL100066961_L01_554 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618218 RB1227 CL100066961_L01_554 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666068 CL100066961_L01_556 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618219 RB1232 CL100066961_L01_556 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666069 CL100066961_L02_557 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618220 RB1233 CL100066961_L02_557 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666070 CL100066961_L02_558 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618221 RB1235 CL100066961_L02_558 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666071 CL100078894_L01_537 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618222 M1001 CL100078894_L01_537 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666072 CL100078894_L01_538 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618223 M1002 CL100078894_L01_538 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666073 CL100078894_L01_539 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618224 M1003 CL100078894_L01_539 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666074 CL100078894_L01_540 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618225 M1004 CL100078894_L01_540 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666075 CL100078894_L02_541 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618226 M1006 CL100078894_L02_541 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666076 CL100078894_L02_542 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618227 M1007 CL100078894_L02_542 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666077 CL100065783_L01_read_4 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618228 M641 CL100065783_L01_read_4 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666078 CL100078894_L02_543 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618229 M1010 CL100078894_L02_543 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666079 CL100078894_L02_544 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618230 M1011 CL100078894_L02_544 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666080 CL100078894_L02_545 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618231 M1013 CL100078894_L02_545 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666081 CL100078894_L02_546 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618232 M1014 CL100078894_L02_546 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666082 CL100078894_L02_547 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618233 M1016 CL100078894_L02_547 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666083 CL100078894_L02_548 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618234 M1019 CL100078894_L02_548 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666084 CL100079849_L01_501 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618235 M1021 CL100079849_L01_501 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666085 CL100079849_L01_502 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618236 M988 CL100079849_L01_502 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666086 CL100079849_L01_504 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618237 M993 CL100079849_L01_504 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666087 CL100065711_L01_read_6 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618238 M855 CL100065711_L01_read_6 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666088 CL100066961_L02_560 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618239 RB1242 CL100066961_L02_560 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666089 CL100066961_L02_561 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618240 RB1243 CL100066961_L02_561 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666090 CL100066961_L02_562 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618241 RB1244 CL100066961_L02_562 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666091 CL100066961_L02_563 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618242 RB1249 CL100066961_L02_563 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666092 CL100066961_L02_564 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618243 RB1253 CL100066961_L02_564 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666093 CL100066863_L02_565 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618244 RB1254 CL100066863_L02_565 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666094 CL100066863_L02_566 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618245 RB1255 CL100066863_L02_566 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666095 CL100066863_L02_568 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618246 RB1261 CL100066863_L02_568 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666096 CL100066863_L02_569 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618247 RB1262 CL100066863_L02_569 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666097 CL100066863_L02_571 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618248 RB1270 CL100066863_L02_571 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666098 CL100065711_L01_read_7 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618249 M2 CL100065711_L01_read_7 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666099 CL100066863_L02_572 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618250 RB1271 CL100066863_L02_572 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666100 CL100066962_L01_573 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618251 RB1273 CL100066962_L01_573 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666101 CL100066962_L01_574 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618252 RB1274 CL100066962_L01_574 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666102 CL100066962_L01_575 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618253 RB1275 CL100066962_L01_575 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666103 CL100079849_L01_505 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618254 M994 CL100079849_L01_505 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666104 CL100065783_L01_read_5 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618255 M642 CL100065783_L01_read_5 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666105 CL100079849_L01_506 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618256 M996 CL100079849_L01_506 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666106 CL100079849_L01_508 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618257 M999 CL100079849_L01_508 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666107 CL100079849_L02_509 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618258 M1032 CL100079849_L02_509 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666108 CL100079849_L02_510 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618259 M1037 CL100079849_L02_510 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666109 CL100079849_L02_511 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618260 M1039 CL100079849_L02_511 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666110 CL100079849_L02_512 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618261 M1041 CL100079849_L02_512 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666111 CL100079849_L02_513 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618262 M1043 CL100079849_L02_513 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666112 CL100079849_L02_514 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618263 M1044 CL100079849_L02_514 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666113 CL100079849_L02_515 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618264 M1045 CL100079849_L02_515 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666114 CL100079849_L02_516 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618265 M1046 CL100079849_L02_516 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666115 CL100065783_L01_read_6 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618266 M643 CL100065783_L01_read_6 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666116 CL100078470_L01_517 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618267 M1047 CL100078470_L01_517 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666117 CL100078470_L01_518 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618268 M1051 CL100078470_L01_518 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666118 CL100078470_L01_519 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618269 M1054 CL100078470_L01_519 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666119 CL100066962_L01_577 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618270 RB1278 CL100066962_L01_577 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666120 CL100066962_L01_578 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618271 RB1289 CL100066962_L01_578 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666121 CL100066962_L01_579 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618272 RB1294 CL100066962_L01_579 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666122 CL100066962_L01_580 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618273 RB1295 CL100066962_L01_580 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666123 CL100066962_L02_582 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618274 RB1306 CL100066962_L02_582 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666124 CL100066962_L02_583 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618275 RB899 CL100066962_L02_583 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666125 CL100065711_L01_read_8 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618276 M16 CL100065711_L01_read_8 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666126 CL100066962_L02_584 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618277 RB900 CL100066962_L02_584 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666127 CL100066962_L02_585 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618278 RB999 CL100066962_L02_585 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666128 CL100066962_L02_586 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618279 RB1000 CL100066962_L02_586 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666129 CL100066962_L02_587 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618280 RB1005 CL100066962_L02_587 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666130 CL100066962_L02_588 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618281 RB1006 CL100066962_L02_588 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666131 CL100067044_L01_589 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618282 RB1072 CL100067044_L01_589 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666132 CL100067044_L01_590 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618283 RB1110 CL100067044_L01_590 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666133 CL100067044_L01_591 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618284 RB1111 CL100067044_L01_591 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666134 CL100067044_L01_592 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618285 RB1121 CL100067044_L01_592 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666135 CL100078470_L01_520 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618286 M1056 CL100078470_L01_520 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666136 CL100078470_L01_521 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618287 M1057 CL100078470_L01_521 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666137 CL100078470_L01_522 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618288 M1058 CL100078470_L01_522 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666138 CL100078470_L01_524 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618289 M1060 CL100078470_L01_524 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666139 CL100078470_L02_525 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618290 M1063 CL100078470_L02_525 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666140 CL100078470_L02_526 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618291 M1064 CL100078470_L02_526 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666141 CL100078470_L02_527 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618292 M1066 CL100078470_L02_527 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666142 CL100065783_L01_read_7 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618293 M644 CL100065783_L01_read_7 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666143 CL100078470_L02_528 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618294 M1067 CL100078470_L02_528 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666144 CL100078470_L02_530 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618295 M1070 CL100078470_L02_530 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666145 CL100078470_L02_531 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618296 M1072 CL100078470_L02_531 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666146 CL100078470_L02_532 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618297 M1073 CL100078470_L02_532 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666147 CL100078872_L01_533 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618298 M1074 CL100078872_L01_533 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666148 CL100078872_L01_534 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618299 M1075 CL100078872_L01_534 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666149 CL100078872_L01_535 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618300 M1077 CL100078872_L01_535 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666150 CL100078872_L01_536 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618301 M1078 CL100078872_L01_536 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666151 CL100067044_L01_593 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618302 RB1124 CL100067044_L01_593 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666152 CL100065711_L02_read_9 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618303 M17 CL100065711_L02_read_9 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666153 CL100067044_L01_594 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618304 RB1150 CL100067044_L01_594 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666154 CL100067044_L01_595 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618305 RB1182 CL100067044_L01_595 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666155 CL100067044_L01_596 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618306 RB1185 CL100067044_L01_596 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666156 CL100074000_L01_501 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618307 RB1186 CL100074000_L01_501 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666157 CL100074000_L01_503 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618308 RB1192 CL100074000_L01_503 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666158 CL100074000_L01_504 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618309 RB1193 CL100074000_L01_504 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666159 CL100074000_L01_505 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618310 RB1196 CL100074000_L01_505 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666160 CL100074000_L01_506 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618311 RB1203 CL100074000_L01_506 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666161 CL100074000_L01_507 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618312 RB1225 CL100074000_L01_507 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666162 CL100074000_L01_508 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618313 RB1228 CL100074000_L01_508 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666163 CL100065711_L02_read_10 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618314 M45 CL100065711_L02_read_10 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666164 CL100067044_L02_510 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618315 RB1240 CL100067044_L02_510 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666165 CL100067044_L02_511 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618316 RB1256 CL100067044_L02_511 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666166 CL100067044_L02_512 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618317 RB1263 CL100067044_L02_512 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666167 CL100078872_L01_537 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618318 M1079 CL100078872_L01_537 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666168 CL100078872_L01_538 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618319 M1081 CL100078872_L01_538 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666169 CL100065783_L01_read_8 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618320 M655 CL100065783_L01_read_8 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666170 CL100078872_L01_539 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618321 M1082 CL100078872_L01_539 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666171 CL100078872_L01_540 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618322 M1083 CL100078872_L01_540 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666172 CL100078872_L02_541 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618323 M1085 CL100078872_L02_541 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666173 CL100078872_L02_542 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618324 M1087 CL100078872_L02_542 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666174 CL100078872_L02_543 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618325 M1088 CL100078872_L02_543 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666175 CL100078872_L02_545 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618326 M1090 CL100078872_L02_545 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666176 CL100078872_L02_546 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618327 M1091 CL100078872_L02_546 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666177 CL100078872_L02_547 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618328 M1092 CL100078872_L02_547 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666178 CL100078866_L01_501 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618329 M1094 CL100078866_L01_501 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666179 CL100078866_L01_502 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618330 M1095 CL100078866_L01_502 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666180 CL100065780_L02_read_12 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618331 M475 CL100065780_L02_read_12 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666181 CL100065783_L02_read_9 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618332 M656 CL100065783_L02_read_9 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666182 CL100078866_L01_503 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618333 M1096 CL100078866_L01_503 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666183 CL100067044_L02_513 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618334 RB1264 CL100067044_L02_513 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666184 CL100067044_L02_514 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618335 RB1265 CL100067044_L02_514 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666185 CL100067044_L02_516 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618336 RB1268 CL100067044_L02_516 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666186 CL100067045_L01_517 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618337 RB1272 CL100067045_L01_517 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666187 CL100067045_L01_518 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618338 RB1279 CL100067045_L01_518 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666188 CL100067045_L01_521 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618339 RB1288 CL100067045_L01_521 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666189 CL100067045_L01_522 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618340 RB1290 CL100067045_L01_522 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666190 CL100065711_L02_read_11 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618341 M54 CL100065711_L02_read_11 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666191 CL100067045_L01_523 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618342 RB1291 CL100067045_L01_523 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666192 CL100067045_L01_524 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618343 RB1292 CL100067045_L01_524 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666193 CL100067045_L02_525 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618344 RB1297 CL100067045_L02_525 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666194 CL100067045_L02_526 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618345 RB1298 CL100067045_L02_526 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666195 CL100067045_L02_527 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618346 RB1303 CL100067045_L02_527 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666196 CL100067045_L02_528 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618347 RB1304 CL100067045_L02_528 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666197 CL100067045_L02_530 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618348 RB1307 CL100067045_L02_530 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666198 CL100074000_L02_533 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618349 RB860 CL100074000_L02_533 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666199 CL100078866_L01_504 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618350 M1097 CL100078866_L01_504 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666200 CL100078866_L01_505 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618351 M1100 CL100078866_L01_505 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666201 CL100078866_L01_506 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618352 M1101 CL100078866_L01_506 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666202 CL100078866_L01_507 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618353 M1103 CL100078866_L01_507 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666203 CL100078866_L01_508 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618354 M1113 CL100078866_L01_508 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666204 CL100078866_L02_509 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618355 M1114 CL100078866_L02_509 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666205 CL100078866_L02_510 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618356 M1115 CL100078866_L02_510 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666206 CL100078866_L02_511 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618357 M1118 CL100078866_L02_511 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666207 CL100078866_L02_512 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618358 M1120 CL100078866_L02_512 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666208 CL100065783_L02_read_10 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618359 M663 CL100065783_L02_read_10 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666209 CL100078866_L02_513 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618360 M1122 CL100078866_L02_513 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666210 CL100078866_L02_514 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618361 M1124 CL100078866_L02_514 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666211 CL100078866_L02_515 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618362 M1125 CL100078866_L02_515 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666212 CL100078866_L02_516 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618363 M1126 CL100078866_L02_516 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666213 CL100078857_L01_517 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618364 M1129 CL100078857_L01_517 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666214 CL100078857_L01_518 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618365 M1131 CL100078857_L01_518 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666215 CL100078857_L01_519 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618366 M1133 CL100078857_L01_519 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666216 CL100078857_L01_520 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618367 M1136 CL100078857_L01_520 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666217 CL100078857_L01_521 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618368 M1138 CL100078857_L01_521 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666218 CL100078857_L01_522 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618369 M1139 CL100078857_L01_522 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666219 CL100065783_L02_read_11 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618370 M668 CL100065783_L02_read_11 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666220 CL100078857_L01_523 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618371 M1140 CL100078857_L01_523 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666221 CL100078857_L01_524 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618372 M1141 CL100078857_L01_524 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666222 CL100078857_L02_525 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618373 M1142 CL100078857_L02_525 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666223 CL100078857_L02_526 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618374 M1143 CL100078857_L02_526 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666224 CL100078857_L02_527 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618375 M1144 CL100078857_L02_527 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666225 CL100078857_L02_528 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618376 M209 CL100078857_L02_528 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666226 CL100078857_L02_529 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618377 M219 CL100078857_L02_529 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666227 CL100078857_L02_530 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618378 M261 CL100078857_L02_530 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666228 CL100078857_L02_531 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618379 M269 CL100078857_L02_531 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666229 CL100078857_L02_532 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618380 M284 CL100078857_L02_532 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666230 CL100065783_L02_read_12 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618381 M669 CL100065783_L02_read_12 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666231 CL100074000_L02_534 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618382 RB520 CL100074000_L02_534 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666232 CL100074000_L02_536 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618383 RB540 CL100074000_L02_536 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666233 CL100065711_L02_read_12 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618384 M55 CL100065711_L02_read_12 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666234 CL100074000_L02_537 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618385 RB543 CL100074000_L02_537 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666235 CL100074000_L02_538 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618386 RB556 CL100074000_L02_538 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666236 CL100074000_L02_539 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618387 RB558 CL100074000_L02_539 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666237 CL100074000_L02_540 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618388 RB570 CL100074000_L02_540 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666238 CL100067046_L01_541 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618389 RB593 CL100067046_L01_541 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666239 CL100067046_L01_542 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618390 RB604 CL100067046_L01_542 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666240 CL100067046_L01_544 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618391 RB615 CL100067046_L01_544 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666241 CL100067046_L01_545 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618392 RB712 CL100067046_L01_545 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666242 CL100067046_L01_546 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618393 RB740 CL100067046_L01_546 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666243 CL100067046_L01_547 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618394 RB747 CL100067046_L01_547 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666244 CL100065711_L02_read_13 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618395 M59 CL100065711_L02_read_13 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666245 CL100067046_L01_548 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618396 RB748 CL100067046_L01_548 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666246 CL100067040_L01_577 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618397 RB1302 CL100067040_L01_577 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666247 CL200067201_L01_533 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618398 M300 CL200067201_L01_533 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666248 CL200067201_L01_534 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618399 M745 CL200067201_L01_534 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666249 CL200067201_L01_535 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618400 M746 CL200067201_L01_535 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666250 CL200067201_L01_536 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618401 M750 CL200067201_L01_536 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666251 CL200067201_L01_537 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618402 M760 CL200067201_L01_537 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666252 CL200067201_L01_538 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618403 M777 CL200067201_L01_538 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666253 CL200067201_L01_539 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618404 M779 CL200067201_L01_539 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666254 CL200067201_L01_540 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618405 M780 CL200067201_L01_540 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666255 CL200067201_L02_542 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618406 M1110 CL200067201_L02_542 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666256 CL200067201_L02_543 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618407 M1112 CL200067201_L02_543 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666257 CL100065783_L02_read_13 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618408 M670 CL100065783_L02_read_13 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666258 CL200067201_L02_544 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618409 M1117 CL200067201_L02_544 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666259 CL200067201_L02_545 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618410 M1121 CL200067201_L02_545 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666260 CL200067201_L02_546 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618411 M1123 CL200067201_L02_546 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666261 CL200067201_L02_547 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618412 M1127 CL200067201_L02_547 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666262 CL200067201_L02_548 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618413 M1132 CL200067201_L02_548 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666263 CL100089900_L01_501 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618414 2A1 CL100089900_L01_501 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666264 CL100089900_L01_502 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618415 3A1 CL100089900_L01_502 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666265 CL100089900_L01_503 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618416 3A2 CL100089900_L01_503 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666266 CL100089900_L01_504 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618417 4A1 CL100089900_L01_504 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666267 CL100089900_L01_505 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618418 1B1 CL100089900_L01_505 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666268 CL100065783_L02_read_14 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618419 M671 CL100065783_L02_read_14 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666269 CL100089900_L01_506 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618420 1B2 CL100089900_L01_506 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666270 CL100089900_L01_507 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618421 2B1 CL100089900_L01_507 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666271 CL100089900_L01_508 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618422 3B1 CL100089900_L01_508 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666272 CL100097400_L02_509 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618423 3B2 CL100097400_L02_509 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666273 CL100097400_L02_510 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618424 4B1 CL100097400_L02_510 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666274 CL100097400_L02_511 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618425 1C1 CL100097400_L02_511 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666275 CL100097400_L02_512 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618426 1C2 CL100097400_L02_512 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666276 CL100097400_L02_513 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618427 2C1 CL100097400_L02_513 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666277 CL100097400_L02_514 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618428 2C2 CL100097400_L02_514 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666278 CL100097400_L02_515 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618429 3C1 CL100097400_L02_515 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666279 CL100067040_L01_578 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618430 RB1197 CL100067040_L01_578 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666280 CL100067040_L02_581 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618431 RB816 CL100067040_L02_581 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666281 CL100067040_L02_582 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618433 RB518 CL100067040_L02_582 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666282 CL100067040_L02_583 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618432 RB554 CL100067040_L02_583 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666283 CL100067040_L02_584 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618434 RB560 CL100067040_L02_584 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666284 CL100067040_L02_586 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618435 RB616 CL100067040_L02_586 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666285 CL100067040_L02_587 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618436 RB707 CL100067040_L02_587 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666286 CL100067040_L02_588 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618437 RB715 CL100067040_L02_588 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666287 CL100065783_L02_read_15 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618438 M673 CL100065783_L02_read_15 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666288 CL100097400_L02_516 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618439 3C2 CL100097400_L02_516 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666289 CL100097564_L01_517 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618440 4C1 CL100097564_L01_517 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666290 CL100097564_L01_518 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618441 1D1 CL100097564_L01_518 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666291 CL100097564_L01_519 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618442 1D2 CL100097564_L01_519 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666292 CL100097564_L01_520 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618443 2D1 CL100097564_L01_520 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666293 CL100097564_L01_521 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618444 3D1 CL100097564_L01_521 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666294 CL100097564_L01_522 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618445 3D2 CL100097564_L01_522 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666295 CL100097564_L01_523 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618446 4D1 CL100097564_L01_523 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666296 CL100097564_L01_524 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618447 1F1 CL100097564_L01_524 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666297 CL100097565_L02_525 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618448 1F2 CL100097565_L02_525 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666298 CL100065783_L02_read_16 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618449 M686 CL100065783_L02_read_16 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666299 CL100097565_L02_526 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618450 2F1 CL100097565_L02_526 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666300 CL100097565_L02_527 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618451 3F1 CL100097565_L02_527 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666301 CL100097565_L02_528 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618453 3F2 CL100097565_L02_528 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666302 CL100097565_L02_529 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618452 4F1 CL100097565_L02_529 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666303 CL100097565_L02_530 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618454 4F2 CL100097565_L02_530 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666304 CL100097565_L02_531 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618455 1G1 CL100097565_L02_531 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666305 CL100097565_L02_532 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618456 1G2 CL100097565_L02_532 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666306 CL100097566_L01_533 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618457 2G1 CL100097566_L01_533 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666307 CL100097566_L01_534 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618458 3G1 CL100097566_L01_534 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666308 CL100097566_L01_535 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618459 3G2 CL100097566_L01_535 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666309 CL100065784_L01_read_1 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618460 M687 CL100065784_L01_read_1 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666310 CL100097566_L01_536 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618461 4G1 CL100097566_L01_536 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666311 CL100097566_L01_537 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618462 4G2 CL100097566_L01_537 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666312 CL100097566_L01_538 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618463 1H1 CL100097566_L01_538 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666313 CL100097566_L01_539 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618464 2H1 CL100097566_L01_539 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666314 CL100097566_L01_540 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618465 3H1 CL100097566_L01_540 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666315 CL100097566_L02_541 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618466 3H2 CL100097566_L02_541 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666316 CL100097566_L02_542 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618467 4H1 CL100097566_L02_542 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666317 CL100097566_L02_543 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618468 E295 CL100097566_L02_543 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666318 CL100097566_L02_544 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618469 E296 CL100097566_L02_544 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666319 CL100097566_L02_545 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618470 1A1 CL100097566_L02_545 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666320 CL100065784_L01_read_2 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618471 M688 CL100065784_L01_read_2 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666321 CL100097566_L02_546 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618472 1A2 CL100097566_L02_546 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666322 CL100097566_L02_547 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618473 E218 CL100097566_L02_547 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666323 CL100097566_L02_548 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618474 E219 CL100097566_L02_548 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666324 CL100086744_L01_501 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618475 E220 CL100086744_L01_501 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666325 CL100086744_L01_502 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618476 E221 CL100086744_L01_502 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666326 CL100086744_L01_503 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618478 E222 CL100086744_L01_503 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666327 CL100086744_L01_504 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618477 E223 CL100086744_L01_504 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666328 CL100086744_L01_505 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618479 E224 CL100086744_L01_505 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666329 CL100086744_L01_506 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618480 E228 CL100086744_L01_506 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666330 CL100086744_L01_507 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618481 E229 CL100086744_L01_507 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666331 CL100065780_L02_read_13 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618482 M476 CL100065780_L02_read_13 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666332 CL100065784_L01_read_3 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618483 M689 CL100065784_L01_read_3 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666333 CL100086744_L01_508 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618484 E230 CL100086744_L01_508 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666334 CL100100390_L02_509 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618485 E231 CL100100390_L02_509 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666335 CL100100390_L02_510 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618486 E232 CL100100390_L02_510 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666336 CL100100390_L02_511 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618487 E233 CL100100390_L02_511 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666337 CL100100390_L02_512 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618488 E234 CL100100390_L02_512 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666338 CL100100390_L02_513 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618489 E235 CL100100390_L02_513 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666339 CL100100390_L02_514 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618490 E236 CL100100390_L02_514 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666340 CL100100390_L02_516 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618492 E244 CL100100390_L02_516 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666341 CL100086730_L01_517 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618491 E250 CL100086730_L01_517 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666342 CL100086730_L01_518 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618493 E251 CL100086730_L01_518 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666343 CL100065784_L01_read_4 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618494 M690 CL100065784_L01_read_4 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666344 CL100086730_L01_519 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618495 E252 CL100086730_L01_519 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666345 CL100086730_L01_520 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618496 E258 CL100086730_L01_520 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666346 CL100086730_L01_521 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618498 E259 CL100086730_L01_521 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666347 CL100086730_L01_523 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618497 E261 CL100086730_L01_523 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666348 CL100086730_L01_524 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618499 E268 CL100086730_L01_524 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666349 CL100089900_L02_525 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618501 E270 CL100089900_L02_525 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666350 CL100089900_L02_526 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618500 E271 CL100089900_L02_526 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666351 CL100089900_L02_527 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618502 E272 CL100089900_L02_527 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666352 CL100089900_L02_528 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618503 E274 CL100089900_L02_528 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666353 CL100089900_L02_529 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618504 E275 CL100089900_L02_529 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666354 CL100065784_L01_read_5 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618505 M691 CL100065784_L01_read_5 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666355 CL100089900_L02_530 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618506 E276 CL100089900_L02_530 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666356 CL100089900_L02_531 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618508 E280 CL100089900_L02_531 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666357 CL100089900_L02_532 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618507 E285 CL100089900_L02_532 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666358 CL100086730_L02_503 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618509 E240 CL100086730_L02_503 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666359 CL100086730_L02_504 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618511 E242 CL100086730_L02_504 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666360 CL100086730_L02_505 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618510 E243 CL100086730_L02_505 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666361 CL100086730_L02_507 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618512 E273 CL100086730_L02_507 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666362 CL100086566_L02_530 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618513 2A3 CL100086566_L02_530 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666363 CL100086566_L02_531 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618514 4A3 CL100086566_L02_531 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666364 CL100086566_L02_532 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618516 2C3 CL100086566_L02_532 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666365 CL100065784_L01_read_6 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618515 M692 CL100065784_L01_read_6 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666366 CL100091146_L01_533 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618517 4C3 CL100091146_L01_533 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666367 CL100091146_L01_534 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618518 2D3 CL100091146_L01_534 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666368 CL100091146_L01_535 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618519 4D3 CL100091146_L01_535 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666369 CL100091146_L02_543 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618520 2F3 CL100091146_L02_543 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666370 CL100091146_L02_544 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618521 4F3 CL100091146_L02_544 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666371 CL100091146_L02_545 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618522 2H4 CL100091146_L02_545 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666372 CL100091146_L02_546 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618523 4H4 CL100091146_L02_546 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666373 CL100091146_L02_547 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618524 2H3 CL100091146_L02_547 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666374 CL100091146_L02_548 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618525 4H3 CL100091146_L02_548 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666375 CL100065780_L01_read_7 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618526 M406 CL100065780_L01_read_7 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666376 CL100065780_L01_read_8 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618527 M466 CL100065780_L01_read_8 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666377 CL100065781_L01_read_1 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618528 M482 CL100065781_L01_read_1 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666378 CL100065711_L02_read_14 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618529 M124 CL100065711_L02_read_14 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666379 CL100065711_L02_read_15 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618530 M149 CL100065711_L02_read_15 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666380 CL100065711_L02_read_16 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618531 M156 CL100065711_L02_read_16 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666381 CL100065712_L01_read_1 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618532 M197 CL100065712_L01_read_1 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666382 CL100065712_L01_read_2 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618533 M30 CL100065712_L01_read_2 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666383 CL100065712_L01_read_3 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618534 M48 CL100065712_L01_read_3 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666384 CL100065712_L01_read_4 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618535 M56 CL100065712_L01_read_4 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666385 CL100065712_L01_read_5 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618536 M57 CL100065712_L01_read_5 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666386 CL100065712_L01_read_6 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618537 M58 CL100065712_L01_read_6 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666387 CL100065712_L01_read_7 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618538 M85 CL100065712_L01_read_7 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666388 CL100065781_L01_read_2 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618539 M485 CL100065781_L01_read_2 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666389 CL100065712_L01_read_8 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618540 M95 CL100065712_L01_read_8 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666390 CL100065712_L02_read_9 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618541 M99 CL100065712_L02_read_9 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666391 CL100066433_L01_read_6 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618542 M455 CL100066433_L01_read_6 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666392 CL100066433_L01_read_8 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618543 M727 CL100066433_L01_read_8 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666393 CL100066433_L02_read_9 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618544 M734 CL100066433_L02_read_9 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666394 CL100066433_L02_read_12 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618545 M772 CL100066433_L02_read_12 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666395 CL100066433_L02_read_15 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618546 M841 CL100066433_L02_read_15 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666396 CL100066434_L01_read_1 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618547 M908 CL100066434_L01_read_1 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666397 CL100066434_L01_read_4 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618548 M930 CL100066434_L01_read_4 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666398 CL100066434_L01_read_6 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618551 M974 CL100066434_L01_read_6 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666399 CL100065781_L02_read_16 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618550 M604 CL100065781_L02_read_16 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666400 CL100066434_L01_read_7 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618549 M215 CL100066434_L01_read_7 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666401 CL100066434_L01_read_8 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618552 M200 CL100066434_L01_read_8 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666402 CL100066434_L02_read_10 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618553 M203 CL100066434_L02_read_10 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666403 CL100066434_L02_read_11 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618554 M205 CL100066434_L02_read_11 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666404 CL100066434_L02_read_12 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618555 M210 CL100066434_L02_read_12 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666405 CL100066434_L02_read_13 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618557 M241 CL100066434_L02_read_13 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666406 CL100066434_L02_read_15 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618556 M278 CL100066434_L02_read_15 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666407 CL100140828_L02_531 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618558 E312 CL100140828_L02_531 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666408 CL100140828_L02_532 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618559 E315 CL100140828_L02_532 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666409 CL100065780_L01_read_1 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618560 RB405 CL100065780_L01_read_1 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666410 CL100065780_L01_read_2 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618561 RB407 CL100065780_L01_read_2 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666411 CL100065780_L01_read_3 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618562 RB412 CL100065780_L01_read_3 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666412 CL100065780_L01_read_4 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618563 RB416 CL100065780_L01_read_4 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666413 CL100065780_L01_read_5 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618565 RB568 CL100065780_L01_read_5 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666414 CL100065780_L01_read_6 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618564 RB645 CL100065780_L01_read_6 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666415 CL100066881_L01_read_1 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618566 RB636 CL100066881_L01_read_1 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666416 CL100065710_L01_read_5 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618567 M235 CL100065710_L01_read_5 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666417 CL100056334_L01_501 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618568 RB705 CL100056334_L01_501 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666418 CL100056334_L01_502 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618569 RB710 CL100056334_L01_502 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666419 CL100056334_L01_503 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618570 RB718 CL100056334_L01_503 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666420 CL100056334_L01_504 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618571 RB731 CL100056334_L01_504 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666421 CL100056334_L01_505 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618572 RB741 CL100056334_L01_505 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666422 CL100056334_L01_506 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618574 RB765 CL100056334_L01_506 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666423 CL100066434_L02_read_16 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618573 M283 CL100066434_L02_read_16 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666424 CL100067041_L02_read_1 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618575 M291 CL100067041_L02_read_1 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666425 CL100067041_L02_read_2 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618576 M299 CL100067041_L02_read_2 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666426 CL100065782_L01_read_1 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618577 M605 CL100065782_L01_read_1 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666427 CL100067041_L02_read_3 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618579 M748 CL100067041_L02_read_3 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666428 CL100067041_L02_read_4 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618578 M751 CL100067041_L02_read_4 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666429 CL100067041_L02_read_5 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618580 M753 CL100067041_L02_read_5 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666430 CL100067041_L02_read_6 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618581 M811 CL100067041_L02_read_6 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666431 CL100067041_L02_read_7 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618583 M856 CL100067041_L02_read_7 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666432 CL100067041_L02_read_8 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618582 M43 CL100067041_L02_read_8 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666433 CL100066880_L01_read_9 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618586 M68 CL100066880_L01_read_9 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666434 CL100066880_L01_read_10 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618584 M104 CL100066880_L01_read_10 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666435 CL100066880_L01_read_11 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618585 M226 CL100066880_L01_read_11 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666436 CL100066880_L01_read_12 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618587 M232 CL100066880_L01_read_12 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666437 CL100065782_L01_read_2 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618588 M607 CL100065782_L01_read_2 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666438 CL100066880_L01_read_13 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618589 M234 CL100066880_L01_read_13 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666439 CL100066880_L01_read_14 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618590 M183 CL100066880_L01_read_14 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666440 CL100066880_L01_read_15 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618591 M194 CL100066880_L01_read_15 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666441 CL100066880_L01_read_16 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618592 M195 CL100066880_L01_read_16 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666442 CL100066435_L02_read_1 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618593 M213 CL100066435_L02_read_1 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666443 CL100066435_L02_read_2 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618594 M266 CL100066435_L02_read_2 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666444 CL100066435_L02_read_3 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618595 M280 CL100066435_L02_read_3 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666445 CL100066435_L02_read_4 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618597 M294 CL100066435_L02_read_4 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666446 CL100066435_L02_read_5 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618596 M297 CL100066435_L02_read_5 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666447 CL100066435_L02_read_6 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618598 M310 CL100066435_L02_read_6 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666448 CL100065782_L01_read_3 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618599 M608 CL100065782_L01_read_3 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666449 CL100066435_L02_read_7 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618600 M339 CL100066435_L02_read_7 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666450 CL100066435_L02_read_8 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618601 M364 CL100066435_L02_read_8 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666451 CL100066880_L02_read_10 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618602 M743 CL100066880_L02_read_10 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666452 CL100066880_L02_read_11 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618603 M244 CL100066880_L02_read_11 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666453 CL100066880_L02_read_12 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618604 M250 CL100066880_L02_read_12 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666454 CL100066880_L02_read_13 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618607 M800 CL100066880_L02_read_13 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666455 CL100056334_L01_507 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618605 RB770 CL100056334_L01_507 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666456 CL100056334_L02_515 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618606 RB771 CL100056334_L02_515 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666457 CL100056334_L02_516 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618609 RB772 CL100056334_L02_516 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666458 CL100056335_L01_501 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618608 RB778 CL100056335_L01_501 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666459 CL100065710_L01_read_6 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618610 M242 CL100065710_L01_read_6 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666460 CL100056335_L01_502 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618612 RB779 CL100056335_L01_502 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666461 CL100056335_L01_503 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618611 RB781 CL100056335_L01_503 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666462 CL100056335_L01_504 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618613 RB783 CL100056335_L01_504 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666463 CL100056335_L01_505 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618615 RB791 CL100056335_L01_505 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666464 CL100056335_L01_506 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618614 RB799 CL100056335_L01_506 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666465 CL100056335_L02_501 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618618 RB851 CL100056335_L02_501 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666466 CL100056335_L02_502 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618616 RB852 CL100056335_L02_502 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666467 CL100056335_L02_503 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618617 RB519 CL100056335_L02_503 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666468 CL100056335_L02_504 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618619 RB521 CL100056335_L02_504 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666469 CL100056335_L02_505 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618620 RB522 CL100056335_L02_505 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666470 CL100065710_L01_read_7 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618621 M262 CL100065710_L01_read_7 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666471 CL100066882_L02_read_12 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618622 M535 CL100066882_L02_read_12 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666472 CL100066882_L02_read_13 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618623 M540 CL100066882_L02_read_13 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666473 CL100066882_L02_read_14 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618624 M543 CL100066882_L02_read_14 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666474 CL100066882_L02_read_15 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618625 M545 CL100066882_L02_read_15 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666475 CL100066882_L02_read_16 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618626 M546 CL100066882_L02_read_16 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666476 CL100066987_L01_read_1 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618627 M547 CL100066987_L01_read_1 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666477 CL100065782_L01_read_7 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618629 M613 CL100065782_L01_read_7 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666478 CL100066987_L01_read_2 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618628 M548 CL100066987_L01_read_2 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666479 CL100066987_L01_read_3 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618631 M549 CL100066987_L01_read_3 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666480 CL100066987_L01_read_4 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618630 M550 CL100066987_L01_read_4 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666481 CL100066987_L01_read_5 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618632 M551 CL100066987_L01_read_5 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666482 CL100066987_L01_read_6 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618634 M552 CL100066987_L01_read_6 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666483 CL100066987_L01_read_7 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618633 M554 CL100066987_L01_read_7 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666484 CL100066987_L01_read_8 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618635 M555 CL100066987_L01_read_8 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666485 CL100066987_L02_read_9 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618636 M556 CL100066987_L02_read_9 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666486 CL100066987_L02_read_13 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618637 M562 CL100066987_L02_read_13 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666487 CL100056335_L02_506 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618638 RB523 CL100056335_L02_506 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666488 CL100056335_L02_507 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618642 RB526 CL100056335_L02_507 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666489 CL100056335_L02_508 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618639 RB527 CL100056335_L02_508 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666490 CL100056336_L02_509 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618640 RB577 CL100056336_L02_509 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666491 CL100056336_L02_510 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618641 RB579 CL100056336_L02_510 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666492 CL100056336_L02_511 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618643 RB580 CL100056336_L02_511 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666493 CL100056336_L02_513 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618644 RB586 CL100056336_L02_513 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666494 CL100056336_L02_514 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618646 RB591 CL100056336_L02_514 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666495 CL100056336_L02_515 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618645 RB592 CL100056336_L02_515 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666496 CL100056336_L02_516 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618648 RB835 CL100056336_L02_516 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666497 CL100065780_L02_read_15 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618647 M479 CL100065780_L02_read_15 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666498 CL100065710_L01_read_8 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618650 M270 CL100065710_L01_read_8 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666499 CL100056337_L01_501 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618649 RB595 CL100056337_L01_501 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666500 CL100056337_L01_502 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618651 RB596 CL100056337_L01_502 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666501 CL100056337_L01_503 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618652 RB598 CL100056337_L01_503 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666502 CL100056337_L01_504 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618653 RB599 CL100056337_L01_504 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666503 CL100066854_L01_read_4 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618654 M573 CL100066854_L01_read_4 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666504 CL100065782_L01_read_8 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618655 M615 CL100065782_L01_read_8 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666505 CL100066854_L01_read_7 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618656 M579 CL100066854_L01_read_7 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666506 CL100066854_L01_read_8 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618657 M580 CL100066854_L01_read_8 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666507 CL100066854_L02_read_9 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618658 M581 CL100066854_L02_read_9 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666508 CL100066854_L02_read_13 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618661 M586 CL100066854_L02_read_13 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666509 CL100066854_L02_read_15 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618659 M588 CL100066854_L02_read_15 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666510 CL100066854_L02_read_16 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618660 M589 CL100066854_L02_read_16 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666511 CL100066855_L01_read_1 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618663 M590 CL100066855_L01_read_1 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666512 CL100066855_L01_read_2 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618662 M591 CL100066855_L01_read_2 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666513 CL100066855_L01_read_3 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618664 M593 CL100066855_L01_read_3 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666514 CL100066855_L01_read_4 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618665 M594 CL100066855_L01_read_4 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666515 CL100065782_L02_read_9 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618666 M616 CL100065782_L02_read_9 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666516 CL100066855_L01_read_5 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618667 M618 CL100066855_L01_read_5 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666517 CL100066855_L01_read_6 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618668 M624 CL100066855_L01_read_6 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666518 CL100066855_L01_read_7 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618669 M625 CL100066855_L01_read_7 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666519 CL100056337_L01_505 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618670 RB601 CL100056337_L01_505 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666520 CL100056337_L01_506 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618672 RB602 CL100056337_L01_506 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666521 CL100056337_L01_507 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618671 RB603 CL100056337_L01_507 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666522 CL100056337_L01_508 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618673 RB606 CL100056337_L01_508 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666523 CL100056337_L02_510 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618674 RB611 CL100056337_L02_510 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666524 CL100056337_L02_511 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618677 RB612 CL100056337_L02_511 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666525 CL100065710_L02_read_9 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618675 M296 CL100065710_L02_read_9 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666526 CL100056337_L02_512 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618676 RB614 CL100056337_L02_512 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666527 CL100056337_L02_513 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618678 RB622 CL100056337_L02_513 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666528 CL100056337_L02_514 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618679 RB651 CL100056337_L02_514 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666529 CL100056337_L02_515 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618681 RB656 CL100056337_L02_515 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666530 CL100056338_L01_502 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618680 RB691 CL100056338_L01_502 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666531 CL100056338_L01_503 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618682 RB685 CL100056338_L01_503 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666532 CL100056338_L01_504 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618683 RB692 CL100056338_L01_504 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666533 CL100056338_L01_506 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618684 RB694 CL100056338_L01_506 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666534 CL100056338_L01_507 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618685 RB695 CL100056338_L01_507 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666535 CL100056338_L01_508 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618688 RB696 CL100056338_L01_508 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666536 CL100065710_L02_read_10 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618686 M301 CL100065710_L02_read_10 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666537 CL100056338_L02_509 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618687 RB697 CL100056338_L02_509 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666538 CL100056338_L02_510 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618689 RB702 CL100056338_L02_510 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666539 CL100056338_L02_511 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618690 RB703 CL100056338_L02_511 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666540 CL100056338_L02_513 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618692 RB706 CL100056338_L02_513 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666541 CL100056338_L02_514 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618691 RB714 CL100056338_L02_514 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666542 CL100056338_L02_515 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618693 RB717 CL100056338_L02_515 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666543 CL100056338_L02_516 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618694 RB719 CL100056338_L02_516 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666544 CL100062353_L02_501 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618695 RB720 CL100062353_L02_501 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666545 CL100062353_L02_503 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618699 RB729 CL100062353_L02_503 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666546 CL100062353_L02_504 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618696 RB730 CL100062353_L02_504 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666547 CL100103968_L01_503 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618697 M135 CL100103968_L01_503 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666548 CL100065784_L01_read_7 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618698 M693 CL100065784_L01_read_7 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666549 CL100103968_L01_505 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618701 M259 CL100103968_L01_505 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666550 CL100103968_L01_506 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618700 M287 CL100103968_L01_506 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666551 CL100103968_L01_508 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618702 M379 CL100103968_L01_508 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666552 CL100103968_L02_509 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618703 M385 CL100103968_L02_509 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666553 CL100103968_L02_510 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618707 M390 CL100103968_L02_510 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666554 CL100103968_L02_511 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618704 M391 CL100103968_L02_511 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666555 CL100065712_L02_read_10 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618705 M116 CL100065712_L02_read_10 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666556 CL100065712_L02_read_11 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618706 M119 CL100065712_L02_read_11 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666557 CL100065712_L02_read_12 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618709 M123 CL100065712_L02_read_12 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666558 CL100065712_L02_read_13 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618708 M150 CL100065712_L02_read_13 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666559 CL100065712_L02_read_14 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618710 M151 CL100065712_L02_read_14 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666560 CL100065712_L02_read_15 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618711 M152 CL100065712_L02_read_15 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666561 CL100065712_L02_read_16 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618712 M153 CL100065712_L02_read_16 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666562 CL100066819_L01_read_1 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618714 M246 CL100066819_L01_read_1 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666563 CL100065781_L01_read_3 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618713 M488 CL100065781_L01_read_3 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666564 CL100066819_L01_read_2 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618715 M255 CL100066819_L01_read_2 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666565 CL100066819_L01_read_3 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618716 M648 CL100066819_L01_read_3 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666566 CL100066819_L01_read_4 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618717 M757 CL100066819_L01_read_4 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666567 CL100066819_L01_read_5 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618718 M758 CL100066819_L01_read_5 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666568 CL100066819_L01_read_6 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618719 M761 CL100066819_L01_read_6 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666569 CL100066819_L01_read_7 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618720 M763 CL100066819_L01_read_7 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666570 CL100066819_L01_read_8 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618721 M764 CL100066819_L01_read_8 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666571 CL100103968_L02_512 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618722 M399 CL100103968_L02_512 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666572 CL100103968_L02_513 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618723 M536 CL100103968_L02_513 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666573 CL100103968_L02_514 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618724 M537 CL100103968_L02_514 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666574 CL100103968_L02_515 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618725 M538 CL100103968_L02_515 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666575 CL100065784_L01_read_8 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618727 M694 CL100065784_L01_read_8 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666576 CL100103968_L02_516 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618726 M539 CL100103968_L02_516 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666577 CL100103970_L01_507 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618728 M966 CL100103970_L01_507 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666578 CL100120844_L01_501 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618730 E324 CL100120844_L01_501 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666579 CL100120844_L01_502 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618731 E325 CL100120844_L01_502 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666580 CL100120844_L01_503 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618732 E327 CL100120844_L01_503 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666581 CL100120844_L01_504 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618729 E328 CL100120844_L01_504 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666582 CL100120844_L01_505 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618733 E329 CL100120844_L01_505 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666583 CL100120844_L01_506 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618734 E330 CL100120844_L01_506 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666584 CL100120844_L01_507 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618735 E331 CL100120844_L01_507 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666585 CL100120844_L01_508 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618736 E332 CL100120844_L01_508 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666586 CL100065784_L02_read_9 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618737 M696 CL100065784_L02_read_9 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666587 CL100066819_L02_read_9 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618738 M765 CL100066819_L02_read_9 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666588 CL100066819_L02_read_10 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618739 M767 CL100066819_L02_read_10 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666589 CL100066819_L02_read_11 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618740 M768 CL100066819_L02_read_11 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666590 CL100065781_L01_read_4 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618741 M490 CL100065781_L01_read_4 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666591 CL100066819_L02_read_12 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618742 M769 CL100066819_L02_read_12 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666592 CL100066819_L02_read_13 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618743 M770 CL100066819_L02_read_13 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666593 CL100066819_L02_read_14 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618744 M771 CL100066819_L02_read_14 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666594 CL100066819_L02_read_15 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618745 M773 CL100066819_L02_read_15 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666595 CL100066819_L02_read_16 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618746 M774 CL100066819_L02_read_16 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666596 CL100074169_L01_read_1 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618747 M775 CL100074169_L01_read_1 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666597 CL100074169_L01_read_2 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618748 M776 CL100074169_L01_read_2 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666598 CL100074169_L01_read_3 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618749 M804 CL100074169_L01_read_3 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666599 CL100074169_L01_read_4 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618750 M806 CL100074169_L01_read_4 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666600 CL100074169_L01_read_6 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618752 M809 CL100074169_L01_read_6 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666601 CL100065781_L01_read_5 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618751 M491 CL100065781_L01_read_5 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666602 CL100074169_L01_read_7 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618753 M813 CL100074169_L01_read_7 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666603 CL100120844_L02_501 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618754 E333 CL100120844_L02_501 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666604 CL100120844_L02_502 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618755 E334 CL100120844_L02_502 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666605 CL100120844_L02_503 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618756 E335 CL100120844_L02_503 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666606 CL100120844_L02_504 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618757 E336 CL100120844_L02_504 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666607 CL100120844_L02_505 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618758 E337 CL100120844_L02_505 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666608 CL100120844_L02_506 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618759 E338 CL100120844_L02_506 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666609 CL100120844_L02_507 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618760 E339 CL100120844_L02_507 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666610 CL100120844_L02_508 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618761 E340 CL100120844_L02_508 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666611 CL100120845_L01_501 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618762 E341 CL100120845_L01_501 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666612 CL100120845_L01_502 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618763 E342 CL100120845_L01_502 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666613 CL100065784_L02_read_10 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618764 M719 CL100065784_L02_read_10 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666614 CL100120845_L01_503 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618765 E343 CL100120845_L01_503 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666615 CL100120845_L01_504 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618766 E584 CL100120845_L01_504 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666616 CL100120845_L01_505 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618767 E586 CL100120845_L01_505 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666617 CL100120845_L01_506 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618768 E587 CL100120845_L01_506 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666618 CL100120845_L01_507 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618771 E588 CL100120845_L01_507 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666619 CL100074169_L01_read_8 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618769 M838 CL100074169_L01_read_8 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666620 CL100074169_L02_read_9 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618770 M839 CL100074169_L02_read_9 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666621 CL100074169_L02_read_10 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618772 M840 CL100074169_L02_read_10 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666622 CL100074169_L02_read_11 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618773 M842 CL100074169_L02_read_11 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666623 CL100074169_L02_read_12 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618774 M844 CL100074169_L02_read_12 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666624 CL100074169_L02_read_14 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618775 M846 CL100074169_L02_read_14 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666625 CL100074169_L02_read_15 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618776 M847 CL100074169_L02_read_15 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666626 CL100074232_L01_read_1 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618777 M849 CL100074232_L01_read_1 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666627 CL100074232_L01_read_2 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618780 M850 CL100074232_L01_read_2 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666628 CL100065781_L01_read_6 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618778 M494 CL100065781_L01_read_6 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666629 CL100074232_L01_read_3 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618779 M852 CL100074232_L01_read_3 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666630 CL100074232_L01_read_4 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618781 M853 CL100074232_L01_read_4 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666631 CL100074232_L01_read_5 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618782 M798 CL100074232_L01_read_5 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666632 CL100074232_L01_read_6 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618783 M799 CL100074232_L01_read_6 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666633 CL100074232_L01_read_7 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618784 M801 CL100074232_L01_read_7 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666634 CL100074232_L01_read_8 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618785 M814 CL100074232_L01_read_8 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666635 CL100120845_L01_508 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618786 E591 CL100120845_L01_508 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666636 CL100120845_L02_501 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618788 E592 CL100120845_L02_501 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666637 CL100120845_L02_502 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618787 E594 CL100120845_L02_502 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666638 CL100120845_L02_503 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618789 E596 CL100120845_L02_503 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666639 CL100120845_L02_504 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618790 E597 CL100120845_L02_504 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666640 CL100065784_L02_read_11 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618791 M720 CL100065784_L02_read_11 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666641 CL100120845_L02_505 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618792 E598 CL100120845_L02_505 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666642 CL100120845_L02_506 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618793 E599 CL100120845_L02_506 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666643 CL100120845_L02_507 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618795 E600 CL100120845_L02_507 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666644 CL100120845_L02_508 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618794 E601 CL100120845_L02_508 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666645 CL100120846_L01_501 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618796 E602 CL100120846_L01_501 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666646 CL100120846_L01_502 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618797 E603 CL100120846_L01_502 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666647 CL100120846_L01_503 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618798 E604 CL100120846_L01_503 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666648 CL100120846_L01_504 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618799 E605 CL100120846_L01_504 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666649 CL100120846_L01_505 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618800 E606 CL100120846_L01_505 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666650 CL100120846_L01_506 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618802 E607 CL100120846_L01_506 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666651 CL100074232_L02_read_9 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618801 M835 CL100074232_L02_read_9 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666652 CL100074232_L02_read_10 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618803 M816 CL100074232_L02_read_10 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666653 CL100074232_L02_read_11 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618804 M817 CL100074232_L02_read_11 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666654 CL100074232_L02_read_12 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618805 M818 CL100074232_L02_read_12 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666655 CL100065781_L01_read_7 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618806 M495 CL100065781_L01_read_7 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666656 CL100074232_L02_read_13 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618807 M819 CL100074232_L02_read_13 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666657 CL100074232_L02_read_14 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618808 M832 CL100074232_L02_read_14 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666658 CL100074232_L02_read_15 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618809 M833 CL100074232_L02_read_15 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666659 CL100074232_L02_read_16 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618811 M834 CL100074232_L02_read_16 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666660 CL100067050_L01_read_1 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618810 M815 CL100067050_L01_read_1 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666661 CL100067050_L01_read_2 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618813 M836 CL100067050_L01_read_2 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666662 CL100067050_L01_read_3 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618812 M878 CL100067050_L01_read_3 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666663 CL100067050_L01_read_4 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618814 M879 CL100067050_L01_read_4 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666664 CL100067050_L01_read_5 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618815 M880 CL100067050_L01_read_5 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666665 CL100067050_L01_read_6 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618816 M896 CL100067050_L01_read_6 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666666 CL100065781_L01_read_8 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618818 M497 CL100065781_L01_read_8 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666667 CL100065784_L02_read_13 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618817 M723 CL100065784_L02_read_13 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666668 CL100120846_L01_507 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618819 E608 CL100120846_L01_507 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666669 CL100120846_L01_508 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618820 E609 CL100120846_L01_508 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666670 CL100120846_L02_501 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618822 E610 CL100120846_L02_501 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666671 CL100120846_L02_502 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618821 E611 CL100120846_L02_502 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666672 CL100120846_L02_503 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618823 E612 CL100120846_L02_503 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666673 CL100120846_L02_504 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618824 E613 CL100120846_L02_504 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666674 CL100120846_L02_505 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618825 E614 CL100120846_L02_505 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666675 CL100120846_L02_506 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618827 E615 CL100120846_L02_506 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666676 CL100120847_L01_501 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618826 E451 CL100120847_L01_501 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666677 CL100120847_L01_502 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618828 E453 CL100120847_L01_502 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666678 CL100065780_L02_read_14 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618829 M478 CL100065780_L02_read_14 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666679 CL100065784_L02_read_14 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618830 E103 CL100065784_L02_read_14 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666680 CL100120847_L01_503 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618831 E455 CL100120847_L01_503 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666681 CL100120847_L01_504 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618832 E456 CL100120847_L01_504 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666682 CL100120847_L01_505 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618833 E457 CL100120847_L01_505 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666683 CL100067050_L01_read_7 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618834 M897 CL100067050_L01_read_7 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666684 CL100067050_L01_read_8 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618835 M898 CL100067050_L01_read_8 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666685 CL100067050_L02_read_9 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618837 M899 CL100067050_L02_read_9 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666686 CL100067050_L02_read_10 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618836 M900 CL100067050_L02_read_10 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666687 CL100067050_L02_read_11 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618838 M901 CL100067050_L02_read_11 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666688 CL100067050_L02_read_12 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618839 M902 CL100067050_L02_read_12 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666689 CL100067050_L02_read_13 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618840 M903 CL100067050_L02_read_13 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666690 CL100067050_L02_read_14 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618841 M904 CL100067050_L02_read_14 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666691 CL100067050_L02_read_15 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618842 M905 CL100067050_L02_read_15 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666692 CL100067050_L02_read_16 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618843 M906 CL100067050_L02_read_16 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666693 CL100065781_L02_read_9 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618844 M597 CL100065781_L02_read_9 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666694 CL100066823_L01_read_1 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618845 M907 CL100066823_L01_read_1 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666695 CL100066823_L01_read_2 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618846 M909 CL100066823_L01_read_2 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666696 CL100066823_L01_read_3 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618847 M910 CL100066823_L01_read_3 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666697 CL100066823_L01_read_4 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618848 M912 CL100066823_L01_read_4 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666698 CL100066823_L01_read_5 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618849 M913 CL100066823_L01_read_5 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666699 CL100120847_L01_506 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618850 E434 CL100120847_L01_506 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666700 CL100120847_L01_507 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618851 E435 CL100120847_L01_507 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666701 CL100120847_L01_508 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618853 E438 CL100120847_L01_508 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666702 CL100120847_L02_502 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618852 E458 CL100120847_L02_502 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666703 CL100120847_L02_503 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618854 E459 CL100120847_L02_503 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666704 CL100120847_L02_504 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618855 E460 CL100120847_L02_504 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666705 CL100120847_L02_505 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618856 E461 CL100120847_L02_505 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666706 CL100065784_L02_read_15 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618857 E133 CL100065784_L02_read_15 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666707 CL100120847_L02_506 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618858 E462 CL100120847_L02_506 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666708 CL100120847_L02_507 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618859 E463 CL100120847_L02_507 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666709 CL100140827_L02_501 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618863 O_3 CL100140827_L02_501 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666710 CL100140827_L02_502 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618860 O_5 CL100140827_L02_502 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666711 CL100140827_L02_503 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618861 O_8 CL100140827_L02_503 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666712 CL100140827_L02_504 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618862 O_9 CL100140827_L02_504 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666713 CL100140827_L02_505 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618864 O_29 CL100140827_L02_505 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666714 CL100140827_L02_507 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618865 O_38 CL100140827_L02_507 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666715 CL100066823_L01_read_6 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618866 M914 CL100066823_L01_read_6 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666716 CL100066823_L01_read_7 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618868 M986 CL100066823_L01_read_7 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666717 CL100066823_L01_read_8 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618867 M926 CL100066823_L01_read_8 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666718 CL100066823_L02_read_9 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618869 M928 CL100066823_L02_read_9 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666719 CL100065710_L02_read_12 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618870 M418 CL100065710_L02_read_12 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666720 CL100062353_L02_505 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618871 RB735 CL100062353_L02_505 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666721 CL100062353_L02_506 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618872 RB736 CL100062353_L02_506 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666722 CL100062353_L02_507 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618874 RB738 CL100062353_L02_507 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666723 CL100066855_L01_read_8 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619345 M626 CL100066855_L01_read_8 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666724 CL100066855_L02_read_9 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618873 M629 CL100066855_L02_read_9 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666725 CL100066855_L02_read_10 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618876 M630 CL100066855_L02_read_10 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666726 CL100066855_L02_read_11 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618875 M636 CL100066855_L02_read_11 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666727 CL100066855_L02_read_12 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618877 M640 CL100066855_L02_read_12 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666728 CL100066855_L02_read_13 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618878 M647 CL100066855_L02_read_13 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666729 CL100066855_L02_read_14 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618879 M695 CL100066855_L02_read_14 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666730 CL100065782_L02_read_10 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619347 M617 CL100065782_L02_read_10 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666731 CL100066855_L02_read_15 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619346 M722 CL100066855_L02_read_15 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666732 CL100066855_L02_read_16 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618882 M724 CL100066855_L02_read_16 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666733 CL100066856_L01_read_1 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618881 E095 CL100066856_L01_read_1 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666734 CL100066856_L01_read_2 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618883 E096 CL100066856_L01_read_2 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666735 CL100066856_L01_read_3 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618880 E099 CL100066856_L01_read_3 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666736 CL100066856_L01_read_4 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618884 E102 CL100066856_L01_read_4 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666737 CL100066856_L01_read_5 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618885 E104 CL100066856_L01_read_5 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666738 CL100066856_L01_read_6 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618887 E107 CL100066856_L01_read_6 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666739 CL100066856_L01_read_7 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618886 E108 CL100066856_L01_read_7 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666740 CL100066856_L01_read_8 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618888 E117 CL100066856_L01_read_8 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666741 CL100065782_L02_read_11 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618889 M619 CL100065782_L02_read_11 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666742 CL100066856_L02_read_9 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618890 E125 CL100066856_L02_read_9 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666743 CL100066856_L02_read_10 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618892 E126 CL100066856_L02_read_10 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666744 CL100066856_L02_read_11 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618891 E127 CL100066856_L02_read_11 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666745 CL100066856_L02_read_12 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618893 E128 CL100066856_L02_read_12 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666746 CL100066856_L02_read_13 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618894 E130 CL100066856_L02_read_13 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666747 CL100066856_L02_read_14 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618895 E131 CL100066856_L02_read_14 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666748 CL100066856_L02_read_15 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618896 E132 CL100066856_L02_read_15 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666749 CL100066856_L02_read_16 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618897 E134 CL100066856_L02_read_16 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666750 CL100056339_L02_501 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618898 M97 CL100056339_L02_501 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666751 CL100056339_L02_502 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618899 M98 CL100056339_L02_502 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666752 CL100065782_L02_read_12 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618900 M621 CL100065782_L02_read_12 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666753 CL100056339_L02_503 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618901 M100 CL100056339_L02_503 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666754 CL100056339_L02_504 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618902 M101 CL100056339_L02_504 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666755 CL100062353_L02_508 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618903 RB739 CL100062353_L02_508 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666756 CL100062353_L01_501 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618904 RB892 CL100062353_L01_501 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666757 CL100062353_L01_502 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618905 RB918 CL100062353_L01_502 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666758 CL100062353_L01_503 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618906 RB919 CL100062353_L01_503 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666759 CL100062353_L01_504 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618907 RB939 CL100062353_L01_504 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666760 CL100062353_L01_505 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618908 RB966 CL100062353_L01_505 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666761 CL100062353_L01_506 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618909 RB985 CL100062353_L01_506 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666762 CL100065710_L02_read_13 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618911 M730 CL100065710_L02_read_13 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666763 CL100062353_L01_507 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618910 RB989 CL100062353_L01_507 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666764 CL100062353_L01_508 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618913 RB993 CL100062353_L01_508 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666765 CL100063132_L02_509 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618912 RB994 CL100063132_L02_509 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666766 CL100063132_L02_510 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618914 RB1026 CL100063132_L02_510 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666767 CL100063132_L02_511 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618915 RB1027 CL100063132_L02_511 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666768 CL100063132_L02_512 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618916 RB1028 CL100063132_L02_512 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666769 CL100063132_L02_513 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618917 RB1044 CL100063132_L02_513 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666770 CL100063132_L02_514 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618918 RB1045 CL100063132_L02_514 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666771 CL100056339_L02_505 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618920 M105 CL100056339_L02_505 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666772 CL100056339_L02_506 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618919 M106 CL100056339_L02_506 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666773 CL100056339_L02_507 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618921 M108 CL100056339_L02_507 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666774 CL100056339_L02_508 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618922 M109 CL100056339_L02_508 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666775 CL100056340_L01_509 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618923 M112 CL100056340_L01_509 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666776 CL100056340_L01_510 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618924 M113 CL100056340_L01_510 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666777 CL100056340_L01_511 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618926 M114 CL100056340_L01_511 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666778 CL100056340_L01_512 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618925 M115 CL100056340_L01_512 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666779 CL100065782_L02_read_13 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618927 M622 CL100065782_L02_read_13 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666780 CL100056340_L01_513 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618928 M117 CL100056340_L01_513 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666781 CL100056340_L01_514 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618929 M118 CL100056340_L01_514 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666782 CL100056340_L01_515 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618930 M136 CL100056340_L01_515 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666783 CL100056340_L01_516 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618931 M137 CL100056340_L01_516 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666784 CL100056340_L02_501 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618932 M138 CL100056340_L02_501 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666785 CL100056340_L02_502 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618933 M139 CL100056340_L02_502 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666786 CL100056340_L02_503 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618935 M140 CL100056340_L02_503 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666787 CL100063132_L02_515 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618934 RB1046 CL100063132_L02_515 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666788 CL100063132_L02_516 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618936 RB1047 CL100063132_L02_516 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666789 CL100065710_L02_read_14 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618937 M733 CL100065710_L02_read_14 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666790 CL100066839_L02_518 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618938 RB1068 CL100066839_L02_518 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666791 CL100066839_L02_519 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618939 RB1075 CL100066839_L02_519 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666792 CL100066839_L02_520 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618942 RB1082 CL100066839_L02_520 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666793 CL100066839_L02_521 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618941 RB1083 CL100066839_L02_521 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666794 CL100066839_L02_522 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618940 RB1085 CL100066839_L02_522 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666795 CL100066839_L02_523 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618943 RB1087 CL100066839_L02_523 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666796 CL100066839_L02_524 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618944 RB1088 CL100066839_L02_524 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666797 CL100066953_L01_525 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618945 RB1090 CL100066953_L01_525 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666798 CL100066953_L01_526 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618946 RB1091 CL100066953_L01_526 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666799 CL100066953_L01_527 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618947 RB1142 CL100066953_L01_527 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666800 CL100065710_L02_read_15 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618948 M749 CL100065710_L02_read_15 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666801 CL100066953_L01_528 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618949 RB1156 CL100066953_L01_528 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666802 CL100066953_L01_529 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618950 RB1158 CL100066953_L01_529 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666803 CL100056340_L02_504 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618951 M142 CL100056340_L02_504 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666804 CL100056340_L02_505 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618953 M143 CL100056340_L02_505 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666805 CL100056340_L02_506 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618952 M144 CL100056340_L02_506 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666806 CL100065782_L02_read_14 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618955 M623 CL100065782_L02_read_14 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666807 CL100056340_L02_507 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618954 M145 CL100056340_L02_507 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666808 CL100056340_L02_508 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618956 M146 CL100056340_L02_508 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666809 CL100056343_L01_509 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618957 M147 CL100056343_L01_509 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666810 CL100056343_L01_510 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618959 M148 CL100056343_L01_510 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666811 CL100056343_L01_511 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618958 M254 CL100056343_L01_511 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666812 CL100056343_L01_512 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618960 M645 CL100056343_L01_512 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666813 CL100056343_L01_513 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618961 M646 CL100056343_L01_513 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666814 CL100056343_L01_514 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618962 M649 CL100056343_L01_514 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666815 CL100056343_L01_515 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618963 M650 CL100056343_L01_515 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666816 CL100056343_L01_516 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618964 M651 CL100056343_L01_516 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666817 CL100065780_L02_read_11 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618965 M474 CL100065780_L02_read_11 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666818 CL100065782_L02_read_15 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618967 M627 CL100065782_L02_read_15 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666819 CL100066953_L01_530 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618966 RB1159 CL100066953_L01_530 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666820 CL100066953_L01_531 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618969 RB1160 CL100066953_L01_531 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666821 CL100066953_L01_532 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618968 RB1161 CL100066953_L01_532 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666822 CL100066953_L02_533 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618971 RB1162 CL100066953_L02_533 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666823 CL100066953_L02_534 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618970 RB1164 CL100066953_L02_534 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666824 CL100066953_L02_535 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619348 RB1165 CL100066953_L02_535 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666825 CL100066953_L02_536 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618972 RB1166 CL100066953_L02_536 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666826 CL100066953_L02_537 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618974 RB1167 CL100066953_L02_537 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666827 CL100065710_L02_read_16 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618973 M755 CL100065710_L02_read_16 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666828 CL100066953_L02_538 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618975 RB1169 CL100066953_L02_538 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666829 CL100066953_L02_539 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618976 RB1173 CL100066953_L02_539 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666830 CL100066953_L02_540 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618977 RB1175 CL100066953_L02_540 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666831 CL100066954_L01_541 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618978 RB1177 CL100066954_L01_541 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666832 CL100066954_L01_542 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618979 RB1178 CL100066954_L01_542 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666833 CL100066954_L01_543 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618980 RB1210 CL100066954_L01_543 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666834 CL100066954_L01_544 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618981 RB1215 CL100066954_L01_544 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666835 CL100066954_L01_545 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618982 RB1283 CL100066954_L01_545 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666836 CL100066954_L01_546 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618984 RB1285 CL100066954_L01_546 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666837 CL100066954_L01_547 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618983 RB1315 CL100066954_L01_547 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666838 CL100065711_L01_read_1 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618985 M762 CL100065711_L01_read_1 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666839 CL100066863_L01_594 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618986 RB1163 CL100066863_L01_594 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666840 CL100066863_L01_596 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618987 RB1099 CL100066863_L01_596 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666841 CL100066957_L01_503 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618988 RB1040 CL100066957_L01_503 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666842 CL100066957_L01_504 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618990 RB1089 CL100066957_L01_504 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666843 CL100066957_L01_505 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618989 RB1092 CL100066957_L01_505 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666844 CL100066957_L01_507 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618991 RB1314 CL100066957_L01_507 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666845 CL100066957_L02_510 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618992 RB1180 CL100066957_L02_510 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666846 CL100066957_L02_511 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618993 RB1181 CL100066957_L02_511 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666847 CL100066958_L01_521 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618996 RB1313 CL100066958_L01_521 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666848 CL100066958_L01_523 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618994 RB1250 CL100066958_L01_523 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666849 CL100065711_L01_read_2 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618995 M781 CL100065711_L01_read_2 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666850 CL100066958_L02_525 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618997 RB896 CL100066958_L02_525 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666851 CL100056343_L02_501 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618999 M652 CL100056343_L02_501 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666852 CL100056343_L02_502 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10618998 M653 CL100056343_L02_502 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666853 CL100056343_L02_503 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619000 M654 CL100056343_L02_503 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666854 CL100056343_L02_504 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619001 M657 CL100056343_L02_504 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666855 CL100056343_L02_505 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619002 M658 CL100056343_L02_505 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666856 CL100056343_L02_506 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619003 M659 CL100056343_L02_506 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666857 CL100056343_L02_507 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619006 M660 CL100056343_L02_507 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666858 CL100056343_L02_508 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619004 M661 CL100056343_L02_508 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666859 CL100057026_L01_509 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619005 M662 CL100057026_L01_509 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666860 CL100057026_L01_510 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619007 M3 CL100057026_L01_510 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666861 CL100065782_L02_read_16 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619008 M628 CL100065782_L02_read_16 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666862 CL100057026_L01_511 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619009 M4 CL100057026_L01_511 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666863 CL100057026_L01_512 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619010 M6 CL100057026_L01_512 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666864 CL100057026_L01_513 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619013 M7 CL100057026_L01_513 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666865 CL100057026_L01_514 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619012 M9 CL100057026_L01_514 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666866 CL100057026_L01_515 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619011 M10 CL100057026_L01_515 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666867 CL100057026_L01_516 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619014 M11 CL100057026_L01_516 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666868 CL100067046_L02_549 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619015 M38 CL100067046_L02_549 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666869 CL100067046_L02_550 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619016 M87 CL100067046_L02_550 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666870 CL100067046_L02_551 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619017 M88 CL100067046_L02_551 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666871 CL100067046_L02_552 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619018 M92 CL100067046_L02_552 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666872 CL100065783_L01_read_1 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619019 M632 CL100065783_L01_read_1 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666873 CL100067046_L02_553 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619020 M94 CL100067046_L02_553 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666874 CL100067046_L02_554 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619021 M96 CL100067046_L02_554 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666875 CL100067046_L02_555 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619022 M102 CL100067046_L02_555 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666876 CL100067046_L02_556 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619023 M141 CL100067046_L02_556 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666877 CL100067047_L01_557 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619024 M12 CL100067047_L01_557 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666878 CL100067047_L01_558 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619025 M15 CL100067047_L01_558 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666879 CL100067047_L01_559 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619026 M18 CL100067047_L01_559 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666880 CL100067047_L01_560 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619027 M26 CL100067047_L01_560 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666881 CL100067047_L01_561 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619028 M27 CL100067047_L01_561 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666882 CL100067047_L01_562 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619029 M28 CL100067047_L01_562 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666883 CL100066958_L02_526 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619030 RB901 CL100066958_L02_526 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666884 CL100066958_L02_528 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619031 RB908 CL100066958_L02_528 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666885 CL100066958_L02_529 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619032 RB1003 CL100066958_L02_529 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666886 CL100066958_L02_530 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619033 RB1059 CL100066958_L02_530 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666887 CL100066958_L02_531 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619034 RB1073 CL100066958_L02_531 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666888 CL100066958_L02_532 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619035 RB1308 CL100066958_L02_532 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666889 CL100066959_L01_533 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619036 RB1102 CL100066959_L01_533 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666890 CL100066959_L01_534 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619037 RB1105 CL100066959_L01_534 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666891 CL100066823_L02_read_10 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619038 M929 CL100066823_L02_read_10 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666892 CL100065781_L02_read_10 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619041 M598 CL100065781_L02_read_10 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666893 CL100066823_L02_read_11 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619039 M959 CL100066823_L02_read_11 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666894 CL100066823_L02_read_12 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619040 M960 CL100066823_L02_read_12 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666895 CL100066823_L02_read_13 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619044 M961 CL100066823_L02_read_13 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666896 CL100066823_L02_read_14 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619043 M962 CL100066823_L02_read_14 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666897 CL100066823_L02_read_15 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619042 M970 CL100066823_L02_read_15 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666898 CL100066823_L02_read_16 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619045 M971 CL100066823_L02_read_16 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666899 CL100066428_L01_read_1 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619046 M973 CL100066428_L01_read_1 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666900 CL100066428_L01_read_2 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619047 M975 CL100066428_L01_read_2 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666901 CL100066428_L01_read_3 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619049 M976 CL100066428_L01_read_3 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666902 CL100066428_L01_read_4 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619048 M820 CL100066428_L01_read_4 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666903 CL100140827_L02_508 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619051 O_39 CL100140827_L02_508 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666904 CL100141263_L01_509 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619050 O_41 CL100141263_L01_509 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666905 CL100065784_L02_read_16 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619052 M502 CL100065784_L02_read_16 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666906 CL100141263_L01_510 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619053 O_43 CL100141263_L01_510 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666907 CL100141263_L01_511 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619054 O_44 CL100141263_L01_511 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666908 CL100141263_L01_512 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619055 O_45 CL100141263_L01_512 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666909 CL100141263_L01_513 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619056 O_46 CL100141263_L01_513 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666910 CL100141263_L01_514 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619059 O_48 CL100141263_L01_514 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666911 CL100141263_L01_515 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619057 O_49 CL100141263_L01_515 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666912 CL100141263_L01_516 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619058 O_50 CL100141263_L01_516 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666913 CL100141263_L02_525 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619060 O_52 CL100141263_L02_525 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666914 CL100141263_L02_526 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619061 O_54 CL100141263_L02_526 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666915 CL100141263_L02_527 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619062 O_56 CL100141263_L02_527 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666916 CL100065710_L01_read_1 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619063 M207 CL100065710_L01_read_1 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666917 CL100141263_L02_528 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619064 O_57 CL100141263_L02_528 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666918 CL100141263_L02_529 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619065 O_59 CL100141263_L02_529 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666919 CL100066880_L02_read_14 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619066 M831 CL100066880_L02_read_14 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666920 CL100066880_L02_read_15 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619067 M877 CL100066880_L02_read_15 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666921 CL100066880_L02_read_16 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619068 M915 CL100066880_L02_read_16 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666922 CL100066881_L01_read_2 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619070 M405 CL100066881_L01_read_2 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666923 CL100065782_L01_read_4 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619069 M609 CL100065782_L01_read_4 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666924 CL100066881_L01_read_3 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619071 M965 CL100066881_L01_read_3 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666925 CL100066881_L01_read_4 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619072 M489 CL100066881_L01_read_4 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666926 CL100066881_L01_read_5 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619073 M499 CL100066881_L01_read_5 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666927 CL100066881_L01_read_6 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619074 M500 CL100066881_L01_read_6 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666928 CL100066881_L01_read_7 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619075 M501 CL100066881_L01_read_7 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666929 CL100066881_L02_read_9 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619076 M505 CL100066881_L02_read_9 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666930 CL100066881_L02_read_10 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619077 M506 CL100066881_L02_read_10 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666931 CL100066881_L02_read_11 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619079 M508 CL100066881_L02_read_11 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666932 CL100066881_L02_read_12 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619078 M510 CL100066881_L02_read_12 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666933 CL100066881_L02_read_13 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619080 M512 CL100066881_L02_read_13 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666934 CL100065780_L02_read_10 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619081 M473 CL100065780_L02_read_10 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666935 CL100065780_L02_read_9 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619084 M467 CL100065780_L02_read_9 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666936 CL100065781_L02_read_11 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619083 M599 CL100065781_L02_read_11 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666937 CL100066428_L01_read_5 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619082 M822 CL100066428_L01_read_5 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666938 CL100066428_L01_read_6 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619085 M837 CL100066428_L01_read_6 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666939 CL100066428_L01_read_7 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619086 M865 CL100066428_L01_read_7 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666940 CL100066428_L01_read_8 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619087 M866 CL100066428_L01_read_8 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666941 CL100066428_L02_read_9 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619088 M867 CL100066428_L02_read_9 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666942 CL100066428_L02_read_10 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619089 M870 CL100066428_L02_read_10 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666943 CL100066428_L02_read_11 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619090 M871 CL100066428_L02_read_11 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666944 CL100066428_L02_read_12 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619091 M918 CL100066428_L02_read_12 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666945 CL100066428_L02_read_13 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619092 M919 CL100066428_L02_read_13 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666946 CL100066428_L02_read_14 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619093 M980 CL100066428_L02_read_14 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666947 CL100065781_L02_read_12 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619094 M600 CL100065781_L02_read_12 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666948 CL100066428_L02_read_15 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619095 M981 CL100066428_L02_read_15 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666949 CL100066429_L01_read_1 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619096 M527 CL100066429_L01_read_1 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666950 CL100066429_L01_read_2 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619097 M532 CL100066429_L01_read_2 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666951 CL100066429_L01_read_3 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619098 M533 CL100066429_L01_read_3 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666952 CL100066429_L01_read_4 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619099 M541 CL100066429_L01_read_4 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666953 CL100066429_L01_read_5 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619100 M544 CL100066429_L01_read_5 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666954 CL100066429_L01_read_7 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619101 M585 CL100066429_L01_read_7 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666955 CL100066429_L01_read_8 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619102 M592 CL100066429_L01_read_8 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666956 CL100066429_L02_read_4 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619103 M595 CL100066429_L02_read_4 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666957 CL100066429_L02_read_5 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619104 E097 CL100066429_L02_read_5 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666958 CL100065781_L02_read_13 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619107 M601 CL100065781_L02_read_13 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666959 CL100066429_L02_read_6 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619105 E098 CL100066429_L02_read_6 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666960 CL100066429_L02_read_7 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619106 E100 CL100066429_L02_read_7 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666961 CL100066429_L02_read_8 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619110 E105 CL100066429_L02_read_8 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666962 CL100066430_L01_read_9 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619108 E106 CL100066430_L01_read_9 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666963 CL100066430_L01_read_11 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619109 E110 CL100066430_L01_read_11 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666964 CL100066430_L01_read_12 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619111 E111 CL100066430_L01_read_12 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666965 CL100066430_L01_read_13 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619112 E112 CL100066430_L01_read_13 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666966 CL100066430_L01_read_14 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619113 E113 CL100066430_L01_read_14 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666967 CL100065782_L01_read_5 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619115 M611 CL100065782_L01_read_5 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666968 CL100066881_L02_read_14 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619114 M514 CL100066881_L02_read_14 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666969 CL100066881_L02_read_15 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619116 M515 CL100066881_L02_read_15 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666970 CL100066881_L02_read_16 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619117 M518 CL100066881_L02_read_16 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666971 CL100066882_L01_read_1 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619118 M521 CL100066882_L01_read_1 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666972 CL100066882_L01_read_2 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619119 M522 CL100066882_L01_read_2 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666973 CL100066882_L01_read_3 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619120 M523 CL100066882_L01_read_3 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666974 CL100066882_L01_read_4 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619122 M524 CL100066882_L01_read_4 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666975 CL100066882_L01_read_5 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619121 M525 CL100066882_L01_read_5 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666976 CL100066882_L01_read_6 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619123 M526 CL100066882_L01_read_6 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666977 CL100066882_L01_read_7 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619124 M528 CL100066882_L01_read_7 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666978 CL100065782_L01_read_6 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619125 M612 CL100065782_L01_read_6 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666979 CL100066882_L01_read_8 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619126 M529 CL100066882_L01_read_8 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666980 CL100066882_L02_read_9 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619127 M530 CL100066882_L02_read_9 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666981 CL100066882_L02_read_10 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619128 M531 CL100066882_L02_read_10 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666982 CL100066882_L02_read_11 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619129 M534 CL100066882_L02_read_11 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666983 CL100141263_L02_530 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619130 O_63 CL100141263_L02_530 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666984 CL100141263_L02_531 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619131 O_68 CL100141263_L02_531 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666985 CL100141263_L02_532 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619132 O_70 CL100141263_L02_532 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666986 CL100141220_L01_533 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619133 O_71 CL100141220_L01_533 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666987 CL100141220_L01_534 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619134 O_74 CL100141220_L01_534 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666988 CL100141220_L01_535 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619135 O_77 CL100141220_L01_535 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666989 CL100141220_L01_536 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619136 O_80 CL100141220_L01_536 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666990 CL100141220_L01_537 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619137 O_81 CL100141220_L01_537 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666991 CL100065710_L01_read_2 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619138 M212 CL100065710_L01_read_2 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666992 CL100141220_L01_538 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619139 O_82 CL100141220_L01_538 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666993 CL100141220_L01_539 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619140 O_83 CL100141220_L01_539 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666994 CL100141220_L01_540 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619141 O_85 CL100141220_L01_540 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666995 CL100141264_L01_501 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619142 O_86 CL100141264_L01_501 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666996 CL100141264_L01_502 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619143 O_87 CL100141264_L01_502 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666997 CL100141264_L01_503 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619144 O_89 CL100141264_L01_503 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666998 CL100141264_L01_504 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619145 O_91 CL100141264_L01_504 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12666999 CL100066430_L01_read_16 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619146 E115 CL100066430_L01_read_16 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667000 CL100066431_L02_read_11 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619147 M206 CL100066431_L02_read_11 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667001 CL100065781_L02_read_14 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619148 M602 CL100065781_L02_read_14 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667002 CL100066431_L02_read_15 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619149 M298 CL100066431_L02_read_15 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667003 CL100066431_L02_read_16 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619150 M155 CL100066431_L02_read_16 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667004 CL100066432_L01_read_2 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619151 M166 CL100066432_L01_read_2 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667005 CL100066432_L01_read_3 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619152 M171 CL100066432_L01_read_3 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667006 CL100066432_L01_read_4 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619153 M186 CL100066432_L01_read_4 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667007 CL100066432_L01_read_5 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619154 M190 CL100066432_L01_read_5 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667008 CL100066432_L01_read_6 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619155 M199 CL100066432_L01_read_6 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667009 CL100066432_L02_read_9 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619156 M272 CL100066432_L02_read_9 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667010 CL100066432_L02_read_12 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619157 M316 CL100066432_L02_read_12 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667011 CL100066432_L02_read_14 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619158 M341 CL100066432_L02_read_14 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667012 CL100065781_L02_read_15 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619159 M603 CL100065781_L02_read_15 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667013 CL100066433_L01_read_3 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619160 M415 CL100066433_L01_read_3 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667014 CL100066433_L01_read_5 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619161 M422 CL100066433_L01_read_5 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667015 CL100141264_L01_505 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619163 O_92 CL100141264_L01_505 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667016 CL100141264_L01_506 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619162 O_93 CL100141264_L01_506 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667017 CL100141264_L01_507 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619164 O_94 CL100141264_L01_507 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667018 CL100065710_L01_read_3 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619165 M220 CL100065710_L01_read_3 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667019 CL100141264_L01_508 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619166 O_95 CL100141264_L01_508 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667020 CL100140828_L01_509 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619167 O_96 CL100140828_L01_509 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667021 CL100140828_L01_510 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619168 O_99 CL100140828_L01_510 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667022 CL100140828_L01_511 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619170 O_101 CL100140828_L01_511 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667023 CL100140828_L01_512 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619169 O_104 CL100140828_L01_512 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667024 CL100140828_L01_513 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619171 O_109 CL100140828_L01_513 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667025 CL100140828_L01_514 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619172 O_110 CL100140828_L01_514 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667026 CL100140828_L02_527 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619173 E300 CL100140828_L02_527 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667027 CL100140828_L02_528 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619175 E302 CL100140828_L02_528 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667028 CL100140828_L02_529 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619174 E304 CL100140828_L02_529 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667029 CL100065710_L01_read_4 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619176 M231 CL100065710_L01_read_4 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500 SRX12667030 CL100140828_L02_530 SRP341862 PRJNA767561 RNA sequences for each sample were first reversed transcribed into cDNA following the Smart-seq2 protocol (Picelli et al., 2014),which was then randomly fragmented with Tn5 enzymes and linked with sequencing adapters to obtain a complete cDNA library for each individual sample. Primers were then added to the cDNA libraries for PCR amplification, and fragments ranging between 150 to 350 bp were selected for further cDNA circularization to construct sequencing libraries. The samples were then sequenced on a BGISEQ-500 platform using a 100nt paired-end sequencing protocol. SRS10619177 E308 CL100140828_L02_530 RNA-Seq TRANSCRIPTOMIC RANDOM BGISEQ-500