RNA-Seq: Streptococcus thermophilus S-3 cultured in M17-B

SRX23774800 M17-B_1 RNA-Seq: Streptococcus thermophilus S-3 cultured in M17-B SRP492209 bp0 All mRNA was fragmented into short segments (200nt) by the addition of fragmentation buffer. Double-stranded cDNA was then synthesized using random hexamer primers (Illumina). During the synthesis of the second strand cDNA, dUTP was incorporated in lieu of dTTP. The synthesized cDNA underwent end-repair, phosphorylation, and A base addition as per Illuminas library construction protocol. SRS20600329 M17-B M17-B_1 RNA-Seq TRANSCRIPTOMIC cDNA_randomPriming Illumina NovaSeq 6000 SRX23774801 M17-B_2 RNA-Seq: Streptococcus thermophilus S-3 cultured in M17-B SRP492209 bp0 All mRNA was fragmented into short segments (200nt) by the addition of fragmentation buffer. Double-stranded cDNA was then synthesized using random hexamer primers (Illumina). During the synthesis of the second strand cDNA, dUTP was incorporated in lieu of dTTP. The synthesized cDNA underwent end-repair, phosphorylation, and A base addition as per Illuminas library construction protocol. SRS20600329 M17-B M17-B_2 RNA-Seq TRANSCRIPTOMIC cDNA_randomPriming Illumina NovaSeq 6000 SRX23774802 M17-B_3 RNA-Seq: Streptococcus thermophilus S-3 cultured in M17-B SRP492209 bp0 All mRNA was fragmented into short segments (200nt) by the addition of fragmentation buffer. Double-stranded cDNA was then synthesized using random hexamer primers (Illumina). During the synthesis of the second strand cDNA, dUTP was incorporated in lieu of dTTP. The synthesized cDNA underwent end-repair, phosphorylation, and A base addition as per Illuminas library construction protocol. SRS20600329 M17-B M17-B_3 RNA-Seq TRANSCRIPTOMIC cDNA_randomPriming Illumina NovaSeq 6000 SRX23774803 M17-1 RNA-Seq: Streptococcus thermophilus S-3 cultured in M17 SRP492209 bp0 All mRNA was fragmented into short segments (200nt) by the addition of fragmentation buffer. Double-stranded cDNA was then synthesized using random hexamer primers (Illumina). During the synthesis of the second strand cDNA, dUTP was incorporated in lieu of dTTP. The synthesized cDNA underwent end-repair, phosphorylation, and A base addition as per Illuminas library construction protocol. SRS20600330 M17 M17-1 RNA-Seq TRANSCRIPTOMIC cDNA_randomPriming Illumina NovaSeq 6000 SRX23774804 M17-2 RNA-Seq: Streptococcus thermophilus S-3 cultured in M17 SRP492209 bp0 All mRNA was fragmented into short segments (200nt) by the addition of fragmentation buffer. Double-stranded cDNA was then synthesized using random hexamer primers (Illumina). During the synthesis of the second strand cDNA, dUTP was incorporated in lieu of dTTP. The synthesized cDNA underwent end-repair, phosphorylation, and A base addition as per Illuminas library construction protocol. SRS20600330 M17 M17-2 RNA-Seq TRANSCRIPTOMIC cDNA_randomPriming Illumina NovaSeq 6000 SRX23774805 M17-3 RNA-Seq: Streptococcus thermophilus S-3 cultured in M17 SRP492209 bp0 All mRNA was fragmented into short segments (200nt) by the addition of fragmentation buffer. Double-stranded cDNA was then synthesized using random hexamer primers (Illumina). During the synthesis of the second strand cDNA, dUTP was incorporated in lieu of dTTP. The synthesized cDNA underwent end-repair, phosphorylation, and A base addition as per Illuminas library construction protocol. SRS20600330 M17 M17-3 RNA-Seq TRANSCRIPTOMIC cDNA_randomPriming Illumina NovaSeq 6000 SRX23774806 UM17_1 RNA-Seq: Streptococcus thermophilus S-3 cultured in UM17 SRP492209 bp0 All mRNA was fragmented into short segments (200nt) by the addition of fragmentation buffer. Double-stranded cDNA was then synthesized using random hexamer primers (Illumina). During the synthesis of the second strand cDNA, dUTP was incorporated in lieu of dTTP. The synthesized cDNA underwent end-repair, phosphorylation, and A base addition as per Illuminas library construction protocol. SRS20600331 UM17 UM17_1 RNA-Seq TRANSCRIPTOMIC cDNA_randomPriming Illumina NovaSeq 6000 SRX23774807 UM17_2 RNA-Seq: Streptococcus thermophilus S-3 cultured in UM17 SRP492209 bp0 All mRNA was fragmented into short segments (200nt) by the addition of fragmentation buffer. Double-stranded cDNA was then synthesized using random hexamer primers (Illumina). During the synthesis of the second strand cDNA, dUTP was incorporated in lieu of dTTP. The synthesized cDNA underwent end-repair, phosphorylation, and A base addition as per Illuminas library construction protocol. SRS20600331 UM17 UM17_2 RNA-Seq TRANSCRIPTOMIC cDNA_randomPriming Illumina NovaSeq 6000 SRX23774808 UM17_3 RNA-Seq: Streptococcus thermophilus S-3 cultured in UM17 SRP492209 bp0 All mRNA was fragmented into short segments (200nt) by the addition of fragmentation buffer. Double-stranded cDNA was then synthesized using random hexamer primers (Illumina). During the synthesis of the second strand cDNA, dUTP was incorporated in lieu of dTTP. The synthesized cDNA underwent end-repair, phosphorylation, and A base addition as per Illuminas library construction protocol. SRS20600331 UM17 UM17_3 RNA-Seq TRANSCRIPTOMIC cDNA_randomPriming Illumina NovaSeq 6000