SRX13670370 GSM5782224_r1 SRP354094 PRJNA795680 SRS11555763 GSM5782224 GSM5782224 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670371 GSM5782225_r1 SRP354094 PRJNA795680 SRS11555764 GSM5782225 GSM5782225 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670372 GSM5782226_r1 SRP354094 PRJNA795680 SRS11555765 GSM5782226 GSM5782226 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670373 GSM5782227_r1 SRP354094 PRJNA795680 SRS11555766 GSM5782227 GSM5782227 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670374 GSM5782228_r1 SRP354094 PRJNA795680 SRS11555767 GSM5782228 GSM5782228 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670375 GSM5782229_r1 SRP354094 PRJNA795680 SRS11555768 GSM5782229 GSM5782229 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670376 GSM5782230_r1 SRP354094 PRJNA795680 SRS11555769 GSM5782230 GSM5782230 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670377 GSM5782231_r1 SRP354094 PRJNA795680 SRS11555770 GSM5782231 GSM5782231 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670378 GSM5782232_r1 SRP354094 PRJNA795680 SRS11555771 GSM5782232 GSM5782232 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670379 GSM5782233_r1 SRP354094 PRJNA795680 SRS11555772 GSM5782233 GSM5782233 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670380 GSM5782234_r1 SRP354094 PRJNA795680 SRS11555773 GSM5782234 GSM5782234 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670381 GSM5782235_r1 SRP354094 PRJNA795680 SRS11555774 GSM5782235 GSM5782235 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670382 GSM5782236_r1 SRP354094 PRJNA795680 SRS11555775 GSM5782236 GSM5782236 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670383 GSM5782237_r1 SRP354094 PRJNA795680 SRS11555776 GSM5782237 GSM5782237 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670384 GSM5782238_r1 SRP354094 PRJNA795680 SRS11555777 GSM5782238 GSM5782238 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670385 GSM5782239_r1 SRP354094 PRJNA795680 SRS11555778 GSM5782239 GSM5782239 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670386 GSM5782240_r1 SRP354094 PRJNA795680 SRS11555779 GSM5782240 GSM5782240 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670387 GSM5782241_r1 SRP354094 PRJNA795680 SRS11555780 GSM5782241 GSM5782241 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670388 GSM5782242_r1 SRP354094 PRJNA795680 SRS11555781 GSM5782242 GSM5782242 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670389 GSM5782243_r1 SRP354094 PRJNA795680 SRS11555782 GSM5782243 GSM5782243 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670390 GSM5782244_r1 SRP354094 PRJNA795680 SRS11555783 GSM5782244 GSM5782244 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670391 GSM5782245_r1 SRP354094 PRJNA795680 SRS11555784 GSM5782245 GSM5782245 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670392 GSM5782246_r1 SRP354094 PRJNA795680 SRS11555785 GSM5782246 GSM5782246 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670393 GSM5782247_r1 SRP354094 PRJNA795680 SRS11555786 GSM5782247 GSM5782247 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670394 GSM5782248_r1 SRP354094 PRJNA795680 SRS11555787 GSM5782248 GSM5782248 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670395 GSM5782249_r1 SRP354094 PRJNA795680 SRS11555788 GSM5782249 GSM5782249 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670396 GSM5782250_r1 SRP354094 PRJNA795680 SRS11555789 GSM5782250 GSM5782250 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670397 GSM5782251_r1 SRP354094 PRJNA795680 SRS11555790 GSM5782251 GSM5782251 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670398 GSM5782252_r1 SRP354094 PRJNA795680 SRS11555791 GSM5782252 GSM5782252 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500 SRX13670399 GSM5782253_r1 SRP354094 PRJNA795680 SRS11555792 GSM5782253 GSM5782253 RNA-Seq TRANSCRIPTOMIC cDNA To prepare for the transcriptome sequencing, we performed a germination test of the two lines under the same conditions. For 72-3, germinating seeds at four-time points (0, 6, 12, 24 HAI) were sampled, while 6-time points (0, 6, 12, 24, 36, 48 HAI) of F9721 were sampled for RNA extraction. Three biological replicates were set for each time point of the two lines. Total RNA was extracted using RNA Easy Fast kit DP452 (TianGen BioTech Beijing Corporation). RNA purity, concentration, and integrity were determined using Nano-Drop TM 2000 spectrophotometer (Thermo Scientific, USA) Libraries of each RNA sample were constructed using Illumina Truseq RNA Sample Prep kits. The paired-end of 125 bp sequencing was performed with an Illumina HiSeq2500 sequencer Illumina HiSeq 2500