SRX3384621 GSM2850294 SRP124820 SRS2679991 GSM2850294 RNA-Seq TRANSCRIPTOMIC cDNA cDNA was prepared and amplified as earlier described (Tang et al., 2010). This strategy results in a 3'bias in sequencing. Illumina libraries were prepared as published (Huang et al., 2017). cDNA were fragmented to ~200 bp with Focused-ultrasonicator (Covaris, Woburn, MA) and adaptor ligated libraries were generated using NEBNext II Ultra DNA library Prep Kit for illumina (New England Labs, Ipswich, MA). Single-end 50 bp sequencing was performed with HiSeq1500 (Illumina, San Diego, CA) Illumina HiSeq 2000 gds 302850294 GSM2850294 GEO Accession GSM2850294 SRX3384622 GSM2850295 SRP124820 SRS2679992 GSM2850295 RNA-Seq TRANSCRIPTOMIC cDNA cDNA was prepared and amplified as earlier described (Tang et al., 2010). This strategy results in a 3'bias in sequencing. Illumina libraries were prepared as published (Huang et al., 2017). cDNA were fragmented to ~200 bp with Focused-ultrasonicator (Covaris, Woburn, MA) and adaptor ligated libraries were generated using NEBNext II Ultra DNA library Prep Kit for illumina (New England Labs, Ipswich, MA). Single-end 50 bp sequencing was performed with HiSeq1500 (Illumina, San Diego, CA) Illumina HiSeq 2000 gds 302850295 GSM2850295 GEO Accession GSM2850295 SRX3384623 GSM2850296 SRP124820 SRS2679993 GSM2850296 RNA-Seq TRANSCRIPTOMIC cDNA cDNA was prepared and amplified as earlier described (Tang et al., 2010). This strategy results in a 3'bias in sequencing. Illumina libraries were prepared as published (Huang et al., 2017). cDNA were fragmented to ~200 bp with Focused-ultrasonicator (Covaris, Woburn, MA) and adaptor ligated libraries were generated using NEBNext II Ultra DNA library Prep Kit for illumina (New England Labs, Ipswich, MA). Single-end 50 bp sequencing was performed with HiSeq1500 (Illumina, San Diego, CA) Illumina HiSeq 2000 gds 302850296 GSM2850296 GEO Accession GSM2850296 SRX3384624 GSM2850297 SRP124820 SRS2679994 GSM2850297 RNA-Seq TRANSCRIPTOMIC cDNA cDNA was prepared and amplified as earlier described (Tang et al., 2010). This strategy results in a 3'bias in sequencing. Illumina libraries were prepared as published (Huang et al., 2017). cDNA were fragmented to ~200 bp with Focused-ultrasonicator (Covaris, Woburn, MA) and adaptor ligated libraries were generated using NEBNext II Ultra DNA library Prep Kit for illumina (New England Labs, Ipswich, MA). Single-end 50 bp sequencing was performed with HiSeq1500 (Illumina, San Diego, CA) Illumina HiSeq 2000 gds 302850297 GSM2850297 GEO Accession GSM2850297 SRX3384625 GSM2850298 SRP124820 SRS2679995 GSM2850298 RNA-Seq TRANSCRIPTOMIC cDNA cDNA was prepared and amplified as earlier described (Tang et al., 2010). This strategy results in a 3'bias in sequencing. Illumina libraries were prepared as published (Huang et al., 2017). cDNA were fragmented to ~200 bp with Focused-ultrasonicator (Covaris, Woburn, MA) and adaptor ligated libraries were generated using NEBNext II Ultra DNA library Prep Kit for illumina (New England Labs, Ipswich, MA). Single-end 50 bp sequencing was performed with HiSeq1500 (Illumina, San Diego, CA) Illumina HiSeq 2000 gds 302850298 GSM2850298 GEO Accession GSM2850298 SRX3384626 GSM2850299 SRP124820 SRS2679996 GSM2850299 RNA-Seq TRANSCRIPTOMIC cDNA cDNA was prepared and amplified as earlier described (Tang et al., 2010). This strategy results in a 3'bias in sequencing. Illumina libraries were prepared as published (Huang et al., 2017). cDNA were fragmented to ~200 bp with Focused-ultrasonicator (Covaris, Woburn, MA) and adaptor ligated libraries were generated using NEBNext II Ultra DNA library Prep Kit for illumina (New England Labs, Ipswich, MA). Single-end 50 bp sequencing was performed with HiSeq1500 (Illumina, San Diego, CA) Illumina HiSeq 2000 gds 302850299 GSM2850299 GEO Accession GSM2850299 SRX3384627 GSM2850300 SRP124820 SRS2680010 GSM2850300 RNA-Seq TRANSCRIPTOMIC cDNA cDNA was prepared and amplified as earlier described (Tang et al., 2010). This strategy results in a 3'bias in sequencing. Illumina libraries were prepared as published (Huang et al., 2017). cDNA were fragmented to ~200 bp with Focused-ultrasonicator (Covaris, Woburn, MA) and adaptor ligated libraries were generated using NEBNext II Ultra DNA library Prep Kit for illumina (New England Labs, Ipswich, MA). Single-end 50 bp sequencing was performed with HiSeq1500 (Illumina, San Diego, CA) Illumina HiSeq 2000 gds 302850300 GSM2850300 GEO Accession GSM2850300 SRX3384628 GSM2850301 SRP124820 SRS2679997 GSM2850301 RNA-Seq TRANSCRIPTOMIC cDNA cDNA was prepared and amplified as earlier described (Tang et al., 2010). This strategy results in a 3'bias in sequencing. Illumina libraries were prepared as published (Huang et al., 2017). cDNA were fragmented to ~200 bp with Focused-ultrasonicator (Covaris, Woburn, MA) and adaptor ligated libraries were generated using NEBNext II Ultra DNA library Prep Kit for illumina (New England Labs, Ipswich, MA). Single-end 50 bp sequencing was performed with HiSeq1500 (Illumina, San Diego, CA) Illumina HiSeq 2000 gds 302850301 GSM2850301 GEO Accession GSM2850301 SRX3384629 GSM2850302 SRP124820 SRS2679998 GSM2850302 RNA-Seq TRANSCRIPTOMIC cDNA cDNA was prepared and amplified as earlier described (Tang et al., 2010). This strategy results in a 3'bias in sequencing. Illumina libraries were prepared as published (Huang et al., 2017). cDNA were fragmented to ~200 bp with Focused-ultrasonicator (Covaris, Woburn, MA) and adaptor ligated libraries were generated using NEBNext II Ultra DNA library Prep Kit for illumina (New England Labs, Ipswich, MA). Single-end 50 bp sequencing was performed with HiSeq1500 (Illumina, San Diego, CA) Illumina HiSeq 2000 gds 302850302 GSM2850302 GEO Accession GSM2850302 SRX3384630 GSM2850303 SRP124820 SRS2679999 GSM2850303 RNA-Seq TRANSCRIPTOMIC cDNA cDNA was prepared and amplified as earlier described (Tang et al., 2010). This strategy results in a 3'bias in sequencing. Illumina libraries were prepared as published (Huang et al., 2017). cDNA were fragmented to ~200 bp with Focused-ultrasonicator (Covaris, Woburn, MA) and adaptor ligated libraries were generated using NEBNext II Ultra DNA library Prep Kit for illumina (New England Labs, Ipswich, MA). Single-end 50 bp sequencing was performed with HiSeq1500 (Illumina, San Diego, CA) Illumina HiSeq 2000 gds 302850303 GSM2850303 GEO Accession GSM2850303 SRX3384631 GSM2850304 SRP124820 SRS2680000 GSM2850304 RNA-Seq TRANSCRIPTOMIC cDNA cDNA was prepared and amplified as earlier described (Tang et al., 2010). This strategy results in a 3'bias in sequencing. Illumina libraries were prepared as published (Huang et al., 2017). cDNA were fragmented to ~200 bp with Focused-ultrasonicator (Covaris, Woburn, MA) and adaptor ligated libraries were generated using NEBNext II Ultra DNA library Prep Kit for illumina (New England Labs, Ipswich, MA). Single-end 50 bp sequencing was performed with HiSeq1500 (Illumina, San Diego, CA) Illumina HiSeq 2000 gds 302850304 GSM2850304 GEO Accession GSM2850304 SRX3384632 GSM2850305 SRP124820 SRS2680001 GSM2850305 RNA-Seq TRANSCRIPTOMIC cDNA cDNA was prepared and amplified as earlier described (Tang et al., 2010). This strategy results in a 3'bias in sequencing. Illumina libraries were prepared as published (Huang et al., 2017). cDNA were fragmented to ~200 bp with Focused-ultrasonicator (Covaris, Woburn, MA) and adaptor ligated libraries were generated using NEBNext II Ultra DNA library Prep Kit for illumina (New England Labs, Ipswich, MA). Single-end 50 bp sequencing was performed with HiSeq1500 (Illumina, San Diego, CA) Illumina HiSeq 2000 gds 302850305 GSM2850305 GEO Accession GSM2850305 SRX3384633 GSM2850306 SRP124820 SRS2680002 GSM2850306 RNA-Seq TRANSCRIPTOMIC cDNA cDNA was prepared and amplified as earlier described (Tang et al., 2010). This strategy results in a 3'bias in sequencing. Illumina libraries were prepared as published (Huang et al., 2017). cDNA were fragmented to ~200 bp with Focused-ultrasonicator (Covaris, Woburn, MA) and adaptor ligated libraries were generated using NEBNext II Ultra DNA library Prep Kit for illumina (New England Labs, Ipswich, MA). Single-end 50 bp sequencing was performed with HiSeq1500 (Illumina, San Diego, CA) Illumina HiSeq 2000 gds 302850306 GSM2850306 GEO Accession GSM2850306 SRX3384634 GSM2850307 SRP124820 SRS2680003 GSM2850307 RNA-Seq TRANSCRIPTOMIC cDNA cDNA was prepared and amplified as earlier described (Tang et al., 2010). This strategy results in a 3'bias in sequencing. Illumina libraries were prepared as published (Huang et al., 2017). cDNA were fragmented to ~200 bp with Focused-ultrasonicator (Covaris, Woburn, MA) and adaptor ligated libraries were generated using NEBNext II Ultra DNA library Prep Kit for illumina (New England Labs, Ipswich, MA). Single-end 50 bp sequencing was performed with HiSeq1500 (Illumina, San Diego, CA) Illumina HiSeq 2000 gds 302850307 GSM2850307 GEO Accession GSM2850307 SRX3384635 GSM2850308 SRP124820 SRS2680004 GSM2850308 RNA-Seq TRANSCRIPTOMIC cDNA cDNA was prepared and amplified as earlier described (Tang et al., 2010). This strategy results in a 3'bias in sequencing. Illumina libraries were prepared as published (Huang et al., 2017). cDNA were fragmented to ~200 bp with Focused-ultrasonicator (Covaris, Woburn, MA) and adaptor ligated libraries were generated using NEBNext II Ultra DNA library Prep Kit for illumina (New England Labs, Ipswich, MA). Single-end 50 bp sequencing was performed with HiSeq1500 (Illumina, San Diego, CA) Illumina HiSeq 2000 gds 302850308 GSM2850308 GEO Accession GSM2850308 SRX3384636 GSM2850309 SRP124820 SRS2680005 GSM2850309 RNA-Seq TRANSCRIPTOMIC cDNA cDNA was prepared and amplified as earlier described (Tang et al., 2010). This strategy results in a 3'bias in sequencing. Illumina libraries were prepared as published (Huang et al., 2017). cDNA were fragmented to ~200 bp with Focused-ultrasonicator (Covaris, Woburn, MA) and adaptor ligated libraries were generated using NEBNext II Ultra DNA library Prep Kit for illumina (New England Labs, Ipswich, MA). Single-end 50 bp sequencing was performed with HiSeq1500 (Illumina, San Diego, CA) Illumina HiSeq 2000 gds 302850309 GSM2850309 GEO Accession GSM2850309 SRX3384637 GSM2850310 SRP124820 SRS2680006 GSM2850310 RNA-Seq TRANSCRIPTOMIC cDNA cDNA was prepared and amplified as earlier described (Tang et al., 2010). This strategy results in a 3'bias in sequencing. Illumina libraries were prepared as published (Huang et al., 2017). cDNA were fragmented to ~200 bp with Focused-ultrasonicator (Covaris, Woburn, MA) and adaptor ligated libraries were generated using NEBNext II Ultra DNA library Prep Kit for illumina (New England Labs, Ipswich, MA). Single-end 50 bp sequencing was performed with HiSeq1500 (Illumina, San Diego, CA) Illumina HiSeq 2000 gds 302850310 GSM2850310 GEO Accession GSM2850310 SRX3384638 GSM2850311 SRP124820 SRS2680007 GSM2850311 RNA-Seq TRANSCRIPTOMIC cDNA cDNA was prepared and amplified as earlier described (Tang et al., 2010). This strategy results in a 3'bias in sequencing. Illumina libraries were prepared as published (Huang et al., 2017). cDNA were fragmented to ~200 bp with Focused-ultrasonicator (Covaris, Woburn, MA) and adaptor ligated libraries were generated using NEBNext II Ultra DNA library Prep Kit for illumina (New England Labs, Ipswich, MA). Single-end 50 bp sequencing was performed with HiSeq1500 (Illumina, San Diego, CA) Illumina HiSeq 2000 gds 302850311 GSM2850311 GEO Accession GSM2850311 SRX3384639 GSM2850312 SRP124820 SRS2680008 GSM2850312 RNA-Seq TRANSCRIPTOMIC cDNA cDNA was prepared and amplified as earlier described (Tang et al., 2010). This strategy results in a 3'bias in sequencing. Illumina libraries were prepared as published (Huang et al., 2017). cDNA were fragmented to ~200 bp with Focused-ultrasonicator (Covaris, Woburn, MA) and adaptor ligated libraries were generated using NEBNext II Ultra DNA library Prep Kit for illumina (New England Labs, Ipswich, MA). Single-end 50 bp sequencing was performed with HiSeq1500 (Illumina, San Diego, CA) Illumina HiSeq 2000 gds 302850312 GSM2850312 GEO Accession GSM2850312 SRX3384640 GSM2850313 SRP124820 SRS2680009 GSM2850313 RNA-Seq TRANSCRIPTOMIC cDNA cDNA was prepared and amplified as earlier described (Tang et al., 2010). This strategy results in a 3'bias in sequencing. Illumina libraries were prepared as published (Huang et al., 2017). cDNA were fragmented to ~200 bp with Focused-ultrasonicator (Covaris, Woburn, MA) and adaptor ligated libraries were generated using NEBNext II Ultra DNA library Prep Kit for illumina (New England Labs, Ipswich, MA). Single-end 50 bp sequencing was performed with HiSeq1500 (Illumina, San Diego, CA) Illumina HiSeq 2000 gds 302850313 GSM2850313 GEO Accession GSM2850313