SRX1017185 GSM1674733 SRP057996 SRS928438 GSM1674733 RNA-Seq TRANSCRIPTOMIC cDNA RNA was purified using Rneasy Plus Mini Kit and enriched for Poly(A)-RNA with MicroPoly(A) Purist Kit. The RNA was base-hydrolyzed, dephosphorylated with PNK and purified using RNA Clean & Concentrator kit (Zymo). Poly(A)-tailing was followed by cDNA synthesis using complementary poly(T)-primers containing Illumina adapter sequences. Excess oligo was removed by Exonuclease I and cDNA fragments of were purified using ChIP DNA Clean & Concentrator kit. The recovered cDNA was RNaseH treated and circularized (CircLigase) and amplified for 10 cycles. The final product was ran on 10% TBE gel, gel purified (180-350 bp) and cleaned-up using ChIP DNA clean & Concentrator Kit. Illumina HiSeq 2000 GEO Sample GSM1674733 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1674733 gds 301674733 GEO Accession GSM1674733 SRX1017186 GSM1674734 SRP057996 SRS928436 GSM1674734 RNA-Seq TRANSCRIPTOMIC cDNA RNA was purified using Rneasy Plus Mini Kit and enriched for Poly(A)-RNA with MicroPoly(A) Purist Kit. The RNA was base-hydrolyzed, dephosphorylated with PNK and purified using RNA Clean & Concentrator kit (Zymo). Poly(A)-tailing was followed by cDNA synthesis using complementary poly(T)-primers containing Illumina adapter sequences. Excess oligo was removed by Exonuclease I and cDNA fragments of were purified using ChIP DNA Clean & Concentrator kit. The recovered cDNA was RNaseH treated and circularized (CircLigase) and amplified for 10 cycles. The final product was ran on 10% TBE gel, gel purified (180-350 bp) and cleaned-up using ChIP DNA clean & Concentrator Kit. Illumina HiSeq 2000 GEO Sample GSM1674734 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1674734 gds 301674734 GEO Accession GSM1674734 SRX1017187 GSM1674735 SRP057996 SRS928437 GSM1674735 RNA-Seq TRANSCRIPTOMIC cDNA RNA was purified using Rneasy Plus Mini Kit and enriched for Poly(A)-RNA with MicroPoly(A) Purist Kit. The RNA was base-hydrolyzed, dephosphorylated with PNK and purified using RNA Clean & Concentrator kit (Zymo). Poly(A)-tailing was followed by cDNA synthesis using complementary poly(T)-primers containing Illumina adapter sequences. Excess oligo was removed by Exonuclease I and cDNA fragments of were purified using ChIP DNA Clean & Concentrator kit. The recovered cDNA was RNaseH treated and circularized (CircLigase) and amplified for 10 cycles. The final product was ran on 10% TBE gel, gel purified (180-350 bp) and cleaned-up using ChIP DNA clean & Concentrator Kit. Illumina HiSeq 2000 GEO Sample GSM1674735 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1674735 gds 301674735 GEO Accession GSM1674735 SRX1017188 GSM1674736 SRP057996 SRS928435 GSM1674736 RNA-Seq TRANSCRIPTOMIC cDNA RNA was purified using Rneasy Plus Mini Kit and enriched for Poly(A)-RNA with MicroPoly(A) Purist Kit. The RNA was base-hydrolyzed, dephosphorylated with PNK and purified using RNA Clean & Concentrator kit (Zymo). Poly(A)-tailing was followed by cDNA synthesis using complementary poly(T)-primers containing Illumina adapter sequences. Excess oligo was removed by Exonuclease I and cDNA fragments of were purified using ChIP DNA Clean & Concentrator kit. The recovered cDNA was RNaseH treated and circularized (CircLigase) and amplified for 10 cycles. The final product was ran on 10% TBE gel, gel purified (180-350 bp) and cleaned-up using ChIP DNA clean & Concentrator Kit. Illumina HiSeq 2000 GEO Sample GSM1674736 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1674736 gds 301674736 GEO Accession GSM1674736 SRX1017189 GSM1674737 SRP057996 SRS928434 GSM1674737 RNA-Seq TRANSCRIPTOMIC cDNA RNA was purified using Rneasy Plus Mini Kit and enriched for Poly(A)-RNA with MicroPoly(A) Purist Kit. The RNA was base-hydrolyzed, dephosphorylated with PNK and purified using RNA Clean & Concentrator kit (Zymo). Poly(A)-tailing was followed by cDNA synthesis using complementary poly(T)-primers containing Illumina adapter sequences. Excess oligo was removed by Exonuclease I and cDNA fragments of were purified using ChIP DNA Clean & Concentrator kit. The recovered cDNA was RNaseH treated and circularized (CircLigase) and amplified for 10 cycles. The final product was ran on 10% TBE gel, gel purified (180-350 bp) and cleaned-up using ChIP DNA clean & Concentrator Kit. Illumina HiSeq 2000 GEO Sample GSM1674737 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1674737 gds 301674737 GEO Accession GSM1674737 SRX1017190 GSM1674738 SRP057996 SRS928432 GSM1674738 RNA-Seq TRANSCRIPTOMIC cDNA RNA was purified using Rneasy Plus Mini Kit and enriched for Poly(A)-RNA with MicroPoly(A) Purist Kit. The RNA was base-hydrolyzed, dephosphorylated with PNK and purified using RNA Clean & Concentrator kit (Zymo). Poly(A)-tailing was followed by cDNA synthesis using complementary poly(T)-primers containing Illumina adapter sequences. Excess oligo was removed by Exonuclease I and cDNA fragments of were purified using ChIP DNA Clean & Concentrator kit. The recovered cDNA was RNaseH treated and circularized (CircLigase) and amplified for 10 cycles. The final product was ran on 10% TBE gel, gel purified (180-350 bp) and cleaned-up using ChIP DNA clean & Concentrator Kit. Illumina HiSeq 2000 GEO Sample GSM1674738 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1674738 gds 301674738 GEO Accession GSM1674738 SRX1017191 GSM1674739 SRP057996 SRS928433 GSM1674739 RNA-Seq TRANSCRIPTOMIC cDNA RNA was purified using Rneasy Plus Mini Kit and enriched for Poly(A)-RNA with MicroPoly(A) Purist Kit. The RNA was base-hydrolyzed, dephosphorylated with PNK and purified using RNA Clean & Concentrator kit (Zymo). Poly(A)-tailing was followed by cDNA synthesis using complementary poly(T)-primers containing Illumina adapter sequences. Excess oligo was removed by Exonuclease I and cDNA fragments of were purified using ChIP DNA Clean & Concentrator kit. The recovered cDNA was RNaseH treated and circularized (CircLigase) and amplified for 10 cycles. The final product was ran on 10% TBE gel, gel purified (180-350 bp) and cleaned-up using ChIP DNA clean & Concentrator Kit. Illumina HiSeq 2000 GEO Sample GSM1674739 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1674739 gds 301674739 GEO Accession GSM1674739 SRX1017192 GSM1674740 SRP057996 SRS928431 GSM1674740 RNA-Seq TRANSCRIPTOMIC cDNA RNA was purified using Rneasy Plus Mini Kit and enriched for Poly(A)-RNA with MicroPoly(A) Purist Kit. The RNA was base-hydrolyzed, dephosphorylated with PNK and purified using RNA Clean & Concentrator kit (Zymo). Poly(A)-tailing was followed by cDNA synthesis using complementary poly(T)-primers containing Illumina adapter sequences. Excess oligo was removed by Exonuclease I and cDNA fragments of were purified using ChIP DNA Clean & Concentrator kit. The recovered cDNA was RNaseH treated and circularized (CircLigase) and amplified for 10 cycles. The final product was ran on 10% TBE gel, gel purified (180-350 bp) and cleaned-up using ChIP DNA clean & Concentrator Kit. Illumina HiSeq 2000 GEO Sample GSM1674740 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1674740 gds 301674740 GEO Accession GSM1674740 SRX1017193 GSM1674741 SRP057996 SRS928430 GSM1674741 RNA-Seq TRANSCRIPTOMIC cDNA RNA was purified using Rneasy Plus Mini Kit and enriched for Poly(A)-RNA with MicroPoly(A) Purist Kit. The RNA was base-hydrolyzed, dephosphorylated with PNK and purified using RNA Clean & Concentrator kit (Zymo). Poly(A)-tailing was followed by cDNA synthesis using complementary poly(T)-primers containing Illumina adapter sequences. Excess oligo was removed by Exonuclease I and cDNA fragments of were purified using ChIP DNA Clean & Concentrator kit. The recovered cDNA was RNaseH treated and circularized (CircLigase) and amplified for 10 cycles. The final product was ran on 10% TBE gel, gel purified (180-350 bp) and cleaned-up using ChIP DNA clean & Concentrator Kit. Illumina HiSeq 2000 GEO Sample GSM1674741 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1674741 gds 301674741 GEO Accession GSM1674741 SRX1017194 GSM1674742 SRP057996 SRS928429 GSM1674742 RNA-Seq TRANSCRIPTOMIC cDNA RNA was purified using Rneasy Plus Mini Kit and enriched for Poly(A)-RNA with MicroPoly(A) Purist Kit. The RNA was base-hydrolyzed, dephosphorylated with PNK and purified using RNA Clean & Concentrator kit (Zymo). Poly(A)-tailing was followed by cDNA synthesis using complementary poly(T)-primers containing Illumina adapter sequences. Excess oligo was removed by Exonuclease I and cDNA fragments of were purified using ChIP DNA Clean & Concentrator kit. The recovered cDNA was RNaseH treated and circularized (CircLigase) and amplified for 10 cycles. The final product was ran on 10% TBE gel, gel purified (180-350 bp) and cleaned-up using ChIP DNA clean & Concentrator Kit. Illumina HiSeq 2000 GEO Sample GSM1674742 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1674742 gds 301674742 GEO Accession GSM1674742 SRX1017195 GSM1674743 SRP057996 SRS928428 GSM1674743 RNA-Seq TRANSCRIPTOMIC cDNA RNA was purified using Rneasy Plus Mini Kit and enriched for Poly(A)-RNA with MicroPoly(A) Purist Kit. The RNA was base-hydrolyzed, dephosphorylated with PNK and purified using RNA Clean & Concentrator kit (Zymo). Poly(A)-tailing was followed by cDNA synthesis using complementary poly(T)-primers containing Illumina adapter sequences. Excess oligo was removed by Exonuclease I and cDNA fragments of were purified using ChIP DNA Clean & Concentrator kit. The recovered cDNA was RNaseH treated and circularized (CircLigase) and amplified for 10 cycles. The final product was ran on 10% TBE gel, gel purified (180-350 bp) and cleaned-up using ChIP DNA clean & Concentrator Kit. Illumina HiSeq 2000 GEO Sample GSM1674743 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1674743 gds 301674743 GEO Accession GSM1674743 SRX1017196 GSM1674744 SRP057996 SRS928427 GSM1674744 RNA-Seq TRANSCRIPTOMIC cDNA RNA was purified using Rneasy Plus Mini Kit and enriched for Poly(A)-RNA with MicroPoly(A) Purist Kit. The RNA was base-hydrolyzed, dephosphorylated with PNK and purified using RNA Clean & Concentrator kit (Zymo). Poly(A)-tailing was followed by cDNA synthesis using complementary poly(T)-primers containing Illumina adapter sequences. Excess oligo was removed by Exonuclease I and cDNA fragments of were purified using ChIP DNA Clean & Concentrator kit. The recovered cDNA was RNaseH treated and circularized (CircLigase) and amplified for 10 cycles. The final product was ran on 10% TBE gel, gel purified (180-350 bp) and cleaned-up using ChIP DNA clean & Concentrator Kit. Illumina HiSeq 2000 GEO Sample GSM1674744 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1674744 gds 301674744 GEO Accession GSM1674744 SRX1017197 GSM1674745 SRP057996 SRS928424 GSM1674745 RNA-Seq TRANSCRIPTOMIC cDNA RNA was purified using Rneasy Plus Mini Kit and enriched for Poly(A)-RNA with MicroPoly(A) Purist Kit. The RNA was base-hydrolyzed, dephosphorylated with PNK and purified using RNA Clean & Concentrator kit (Zymo). Poly(A)-tailing was followed by cDNA synthesis using complementary poly(T)-primers containing Illumina adapter sequences. Excess oligo was removed by Exonuclease I and cDNA fragments of were purified using ChIP DNA Clean & Concentrator kit. The recovered cDNA was RNaseH treated and circularized (CircLigase) and amplified for 10 cycles. The final product was ran on 10% TBE gel, gel purified (180-350 bp) and cleaned-up using ChIP DNA clean & Concentrator Kit. Illumina HiSeq 2000 GEO Sample GSM1674745 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1674745 gds 301674745 GEO Accession GSM1674745 SRX1017198 GSM1674746 SRP057996 SRS928425 GSM1674746 RNA-Seq TRANSCRIPTOMIC cDNA RNA was purified using Rneasy Plus Mini Kit and enriched for Poly(A)-RNA with MicroPoly(A) Purist Kit. The RNA was base-hydrolyzed, dephosphorylated with PNK and purified using RNA Clean & Concentrator kit (Zymo). Poly(A)-tailing was followed by cDNA synthesis using complementary poly(T)-primers containing Illumina adapter sequences. Excess oligo was removed by Exonuclease I and cDNA fragments of were purified using ChIP DNA Clean & Concentrator kit. The recovered cDNA was RNaseH treated and circularized (CircLigase) and amplified for 10 cycles. The final product was ran on 10% TBE gel, gel purified (180-350 bp) and cleaned-up using ChIP DNA clean & Concentrator Kit. Illumina HiSeq 2000 GEO Sample GSM1674746 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1674746 gds 301674746 GEO Accession GSM1674746 SRX1017199 GSM1674747 SRP057996 SRS928426 GSM1674747 RNA-Seq TRANSCRIPTOMIC cDNA RNA was purified using Rneasy Plus Mini Kit and enriched for Poly(A)-RNA with MicroPoly(A) Purist Kit. The RNA was base-hydrolyzed, dephosphorylated with PNK and purified using RNA Clean & Concentrator kit (Zymo). Poly(A)-tailing was followed by cDNA synthesis using complementary poly(T)-primers containing Illumina adapter sequences. Excess oligo was removed by Exonuclease I and cDNA fragments of were purified using ChIP DNA Clean & Concentrator kit. The recovered cDNA was RNaseH treated and circularized (CircLigase) and amplified for 10 cycles. The final product was ran on 10% TBE gel, gel purified (180-350 bp) and cleaned-up using ChIP DNA clean & Concentrator Kit. Illumina HiSeq 2000 GEO Sample GSM1674747 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1674747 gds 301674747 GEO Accession GSM1674747 SRX1017200 GSM1674748 SRP057996 SRS928423 GSM1674748 RNA-Seq TRANSCRIPTOMIC cDNA RNA was purified using Rneasy Plus Mini Kit and enriched for Poly(A)-RNA with MicroPoly(A) Purist Kit. The RNA was base-hydrolyzed, dephosphorylated with PNK and purified using RNA Clean & Concentrator kit (Zymo). Poly(A)-tailing was followed by cDNA synthesis using complementary poly(T)-primers containing Illumina adapter sequences. Excess oligo was removed by Exonuclease I and cDNA fragments of were purified using ChIP DNA Clean & Concentrator kit. The recovered cDNA was RNaseH treated and circularized (CircLigase) and amplified for 10 cycles. The final product was ran on 10% TBE gel, gel purified (180-350 bp) and cleaned-up using ChIP DNA clean & Concentrator Kit. Illumina HiSeq 2000 GEO Sample GSM1674748 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1674748 gds 301674748 GEO Accession GSM1674748