SRX4240296 GSM3207041 SRP150876 PRJNA476792 SRS3437743 SAMN09458906 RNA-Seq TRANSCRIPTOMIC cDNA mRNA molecues were captured using bead-bound oligo dT(30). Captured mRNA molecues were reverse transcriped to obtain cDNA which is then amplified by PCR reactions. The cDNA PCR reaction product was then purified with AMPure XP beads. The purified cDNA PCR product was used as the input for Nextera XT reactions to generate sequencing library. NextSeq 500 gds 303207041 GSM3207041 GEO Accession GSM3207041 SRX4240297 GSM3207042 SRP150876 PRJNA476792 SRS3437748 SAMN09458905 RNA-Seq TRANSCRIPTOMIC cDNA mRNA molecues were captured using bead-bound oligo dT(30). Captured mRNA molecues were reverse transcriped to obtain cDNA which is then amplified by PCR reactions. The cDNA PCR reaction product was then purified with AMPure XP beads. The purified cDNA PCR product was used as the input for Nextera XT reactions to generate sequencing library. NextSeq 500 gds 303207042 GSM3207042 GEO Accession GSM3207042 SRX4240298 GSM3207043 SRP150876 PRJNA476792 SRS3437745 SAMN09458904 RNA-Seq TRANSCRIPTOMIC cDNA mRNA molecues were captured using bead-bound oligo dT(30). Captured mRNA molecues were reverse transcriped to obtain cDNA which is then amplified by PCR reactions. The cDNA PCR reaction product was then purified with AMPure XP beads. The purified cDNA PCR product was used as the input for Nextera XT reactions to generate sequencing library. NextSeq 500 gds 303207043 GSM3207043 GEO Accession GSM3207043 SRX4240299 GSM3207044 SRP150876 PRJNA476792 SRS3437747 SAMN09458903 RNA-Seq TRANSCRIPTOMIC cDNA mRNA molecues were captured using bead-bound oligo dT(30). Captured mRNA molecues were reverse transcriped to obtain cDNA which is then amplified by PCR reactions. The cDNA PCR reaction product was then purified with AMPure XP beads. The purified cDNA PCR product was used as the input for Nextera XT reactions to generate sequencing library. NextSeq 500 gds 303207044 GSM3207044 GEO Accession GSM3207044 SRX4240300 GSM3207045 SRP150876 PRJNA476792 SRS3437749 SAMN09458902 RNA-Seq TRANSCRIPTOMIC cDNA mRNA molecues were captured using bead-bound oligo dT(30). Captured mRNA molecues were reverse transcriped to obtain cDNA which is then amplified by PCR reactions. The cDNA PCR reaction product was then purified with AMPure XP beads. The purified cDNA PCR product was used as the input for Nextera XT reactions to generate sequencing library. NextSeq 500 gds 303207045 GSM3207045 GEO Accession GSM3207045 SRX4240301 GSM3207046 SRP150876 PRJNA476792 SRS3437750 SAMN09458901 RNA-Seq TRANSCRIPTOMIC cDNA mRNA molecues were captured using bead-bound oligo dT(30). Captured mRNA molecues were reverse transcriped to obtain cDNA which is then amplified by PCR reactions. The cDNA PCR reaction product was then purified with AMPure XP beads. The purified cDNA PCR product was used as the input for Nextera XT reactions to generate sequencing library. NextSeq 500 gds 303207046 GSM3207046 GEO Accession GSM3207046 SRX4240302 GSM3207047 SRP150876 PRJNA476792 SRS3437744 SAMN09458900 RNA-Seq TRANSCRIPTOMIC cDNA mRNA molecues were captured using bead-bound oligo dT(30). Captured mRNA molecues were reverse transcriped to obtain cDNA which is then amplified by PCR reactions. The cDNA PCR reaction product was then purified with AMPure XP beads. The purified cDNA PCR product was used as the input for Nextera XT reactions to generate sequencing library. NextSeq 500 gds 303207047 GSM3207047 GEO Accession GSM3207047 SRX4240303 GSM3207048 SRP150876 PRJNA476792 SRS3437746 SAMN09458899 RNA-Seq TRANSCRIPTOMIC cDNA mRNA molecues were captured using bead-bound oligo dT(30). Captured mRNA molecues were reverse transcriped to obtain cDNA which is then amplified by PCR reactions. The cDNA PCR reaction product was then purified with AMPure XP beads. The purified cDNA PCR product was used as the input for Nextera XT reactions to generate sequencing library. NextSeq 500 gds 303207048 GSM3207048 GEO Accession GSM3207048 SRX4240304 GSM3207049 SRP150876 PRJNA476792 SRS3437752 SAMN09458898 RNA-Seq TRANSCRIPTOMIC cDNA mRNA molecues were captured using bead-bound oligo dT(30). Captured mRNA molecues were reverse transcriped to obtain cDNA which is then amplified by PCR reactions. The cDNA PCR reaction product was then purified with AMPure XP beads. The purified cDNA PCR product was used as the input for Nextera XT reactions to generate sequencing library. NextSeq 500 gds 303207049 GSM3207049 GEO Accession GSM3207049 SRX4240305 GSM3207050 SRP150876 PRJNA476792 SRS3437751 SAMN09458897 RNA-Seq TRANSCRIPTOMIC cDNA mRNA molecues were captured using bead-bound oligo dT(30). Captured mRNA molecues were reverse transcriped to obtain cDNA which is then amplified by PCR reactions. The cDNA PCR reaction product was then purified with AMPure XP beads. The purified cDNA PCR product was used as the input for Nextera XT reactions to generate sequencing library. NextSeq 500 gds 303207050 GSM3207050 GEO Accession GSM3207050 SRX4240306 GSM3207051 SRP150876 PRJNA476792 SRS3437753 SAMN09458896 OTHER GENOMIC other Drop-Seq beads were vortexed for 1 minute, sonicated for 5 minutes, and incubated at 4°C for 12 hours. The resulting supernatent was used for downstream library construction. The bead-free single-stranded DNAs were hybridized to a primer, and then converted to double-stranded DNA molecules which were then PCR amplified, purified by Ampure XP beads and gel electrophoresis. NextSeq 500 gds 303207051 GSM3207051 GEO Accession GSM3207051