SRX3204180 GSM2790179 SRP118529 SRS2530430 GSM2790179 RNA-Seq TRANSCRIPTOMIC cDNA For each sample, ~20 different plates were frozen and ground in liquid nitrogen. Supernatants were precleared and incubated with EZview Red ANTI-FLAG M2 affinity Gel (Sigma). The beads were removed by spinning and RNA was then extracted using phenol:chloroform. Extracted RNA was processed into sequencing libraries and sequenced at Fasteris (http://www.fasteris.com, Switzerland) using the Illumina MiSeq sequencer Illumina MiSeq gds 302790179 GSM2790179 GEO Accession GSM2790179 SRX3204181 GSM2790180 SRP118529 SRS2530431 GSM2790180 RNA-Seq TRANSCRIPTOMIC cDNA For each sample, ~20 different plates were frozen and ground in liquid nitrogen. Supernatants were precleared and incubated with EZview Red ANTI-FLAG M2 affinity Gel (Sigma). The beads were removed by spinning and RNA was then extracted using phenol:chloroform. Extracted RNA was processed into sequencing libraries and sequenced at Fasteris (http://www.fasteris.com, Switzerland) using the Illumina MiSeq sequencer Illumina MiSeq gds 302790180 GSM2790180 GEO Accession GSM2790180 SRX3204182 GSM2790181 SRP118529 SRS2530432 GSM2790181 RNA-Seq TRANSCRIPTOMIC cDNA For each sample, ~20 different plates were frozen and ground in liquid nitrogen. Supernatants were precleared and incubated with EZview Red ANTI-FLAG M2 affinity Gel (Sigma). The beads were removed by spinning and RNA was then extracted using phenol:chloroform. Extracted RNA was processed into sequencing libraries and sequenced at Fasteris (http://www.fasteris.com, Switzerland) using the Illumina MiSeq sequencer Illumina MiSeq gds 302790181 GSM2790181 GEO Accession GSM2790181 SRX3204183 GSM2790182 SRP118529 SRS2530433 GSM2790182 RNA-Seq TRANSCRIPTOMIC cDNA For each sample, ~20 different plates were frozen and ground in liquid nitrogen. Supernatants were precleared and incubated with EZview Red ANTI-FLAG M2 affinity Gel (Sigma). The beads were removed by spinning and RNA was then extracted using phenol:chloroform. Extracted RNA was processed into sequencing libraries and sequenced at Fasteris (http://www.fasteris.com, Switzerland) using the Illumina MiSeq sequencer Illumina MiSeq gds 302790182 GSM2790182 GEO Accession GSM2790182 SRX3204184 GSM2790183 SRP118529 SRS2530434 GSM2790183 RNA-Seq TRANSCRIPTOMIC cDNA For each sample, ~20 different plates were frozen and ground in liquid nitrogen. Supernatants were precleared and incubated with EZview Red ANTI-FLAG M2 affinity Gel (Sigma). The beads were removed by spinning and RNA was then extracted using phenol:chloroform. Extracted RNA was processed into sequencing libraries and sequenced at Fasteris (http://www.fasteris.com, Switzerland) using the Illumina MiSeq sequencer Illumina MiSeq gds 302790183 GSM2790183 GEO Accession GSM2790183 SRX3204185 GSM2790184 SRP118529 SRS2530435 GSM2790184 RNA-Seq TRANSCRIPTOMIC cDNA For each sample, ~20 different plates were frozen and ground in liquid nitrogen. Supernatants were precleared and incubated with EZview Red ANTI-FLAG M2 affinity Gel (Sigma). The beads were removed by spinning and RNA was then extracted using phenol:chloroform. Extracted RNA was processed into sequencing libraries and sequenced at Fasteris (http://www.fasteris.com, Switzerland) using the Illumina MiSeq sequencer Illumina MiSeq gds 302790184 GSM2790184 GEO Accession GSM2790184 SRX3204186 GSM2790185 SRP118529 SRS2530436 GSM2790185 RNA-Seq TRANSCRIPTOMIC cDNA For each sample, ~20 different plates were frozen and ground in liquid nitrogen. Supernatants were precleared and incubated with EZview Red ANTI-FLAG M2 affinity Gel (Sigma). The beads were removed by spinning and RNA was then extracted using phenol:chloroform. Extracted RNA was processed into sequencing libraries and sequenced at Fasteris (http://www.fasteris.com, Switzerland) using the Illumina MiSeq sequencer Illumina MiSeq gds 302790185 GSM2790185 GEO Accession GSM2790185 SRX3204187 GSM2790186 SRP118529 SRS2530437 GSM2790186 RNA-Seq TRANSCRIPTOMIC cDNA For each sample, ~20 different plates were frozen and ground in liquid nitrogen. Supernatants were precleared and incubated with EZview Red ANTI-FLAG M2 affinity Gel (Sigma). The beads were removed by spinning and RNA was then extracted using phenol:chloroform. Extracted RNA was processed into sequencing libraries and sequenced at Fasteris (http://www.fasteris.com, Switzerland) using the Illumina MiSeq sequencer Illumina MiSeq gds 302790186 GSM2790186 GEO Accession GSM2790186 SRX3204188 GSM2790187 SRP118529 SRS2530438 GSM2790187 RNA-Seq TRANSCRIPTOMIC cDNA For each sample, ~20 different plates were frozen and ground in liquid nitrogen. Supernatants were precleared and incubated with EZview Red ANTI-FLAG M2 affinity Gel (Sigma). The beads were removed by spinning and RNA was then extracted using phenol:chloroform. Extracted RNA was processed into sequencing libraries and sequenced at Fasteris (http://www.fasteris.com, Switzerland) using the Illumina MiSeq sequencer Illumina MiSeq gds 302790187 GSM2790187 GEO Accession GSM2790187 SRX3204189 GSM2790188 SRP118529 SRS2530439 GSM2790188 RNA-Seq TRANSCRIPTOMIC cDNA For each sample, ~20 different plates were frozen and ground in liquid nitrogen. Supernatants were precleared and incubated with EZview Red ANTI-FLAG M2 affinity Gel (Sigma). The beads were removed by spinning and RNA was then extracted using phenol:chloroform. Extracted RNA was processed into sequencing libraries and sequenced at Fasteris (http://www.fasteris.com, Switzerland) using the Illumina MiSeq sequencer Illumina MiSeq gds 302790188 GSM2790188 GEO Accession GSM2790188 SRX3204190 GSM2790189 SRP118529 SRS2530440 GSM2790189 RNA-Seq TRANSCRIPTOMIC cDNA For each sample, ~20 different plates were frozen and ground in liquid nitrogen. Supernatants were precleared and incubated with EZview Red ANTI-FLAG M2 affinity Gel (Sigma). The beads were removed by spinning and RNA was then extracted using phenol:chloroform. Extracted RNA was processed into sequencing libraries and sequenced at Fasteris (http://www.fasteris.com, Switzerland) using the Illumina MiSeq sequencer Illumina MiSeq gds 302790189 GSM2790189 GEO Accession GSM2790189 SRX3204191 GSM2790190 SRP118529 SRS2530441 GSM2790190 RNA-Seq TRANSCRIPTOMIC cDNA For each sample, ~20 different plates were frozen and ground in liquid nitrogen. Supernatants were precleared and incubated with EZview Red ANTI-FLAG M2 affinity Gel (Sigma). The beads were removed by spinning and RNA was then extracted using phenol:chloroform. Extracted RNA was processed into sequencing libraries and sequenced at Fasteris (http://www.fasteris.com, Switzerland) using the Illumina MiSeq sequencer Illumina MiSeq gds 302790190 GSM2790190 GEO Accession GSM2790190 SRX3204192 GSM2790191 SRP118529 SRS2530442 GSM2790191 RNA-Seq TRANSCRIPTOMIC cDNA For each sample, ~20 different plates were frozen and ground in liquid nitrogen. Supernatants were precleared and incubated with EZview Red ANTI-FLAG M2 affinity Gel (Sigma). The beads were removed by spinning and RNA was then extracted using phenol:chloroform. Extracted RNA was processed into sequencing libraries and sequenced at Fasteris (http://www.fasteris.com, Switzerland) using the Illumina MiSeq sequencer Illumina MiSeq gds 302790191 GSM2790191 GEO Accession GSM2790191 SRX3204193 GSM2790192 SRP118529 SRS2530443 GSM2790192 RNA-Seq TRANSCRIPTOMIC cDNA For each sample, ~20 different plates were frozen and ground in liquid nitrogen. Supernatants were precleared and incubated with EZview Red ANTI-FLAG M2 affinity Gel (Sigma). The beads were removed by spinning and RNA was then extracted using phenol:chloroform. Extracted RNA was processed into sequencing libraries and sequenced at Fasteris (http://www.fasteris.com, Switzerland) using the Illumina MiSeq sequencer Illumina MiSeq gds 302790192 GSM2790192 GEO Accession GSM2790192 SRX3204194 GSM2790193 SRP118529 SRS2530444 GSM2790193 RNA-Seq TRANSCRIPTOMIC cDNA For each sample, ~20 different plates were frozen and ground in liquid nitrogen. Supernatants were precleared and incubated with EZview Red ANTI-FLAG M2 affinity Gel (Sigma). The beads were removed by spinning and RNA was then extracted using phenol:chloroform. Extracted RNA was processed into sequencing libraries and sequenced at Fasteris (http://www.fasteris.com, Switzerland) using the Illumina MiSeq sequencer Illumina MiSeq gds 302790193 GSM2790193 GEO Accession GSM2790193 SRX3204195 GSM2790194 SRP118529 SRS2530445 GSM2790194 RNA-Seq TRANSCRIPTOMIC cDNA For each sample, ~20 different plates were frozen and ground in liquid nitrogen. Supernatants were precleared and incubated with EZview Red ANTI-FLAG M2 affinity Gel (Sigma). The beads were removed by spinning and RNA was then extracted using phenol:chloroform. Extracted RNA was processed into sequencing libraries and sequenced at Fasteris (http://www.fasteris.com, Switzerland) using the Illumina MiSeq sequencer Illumina MiSeq gds 302790194 GSM2790194 GEO Accession GSM2790194 SRX3204196 GSM2790195 SRP118529 SRS2530446 GSM2790195 RNA-Seq TRANSCRIPTOMIC cDNA For each sample, ~20 different plates were frozen and ground in liquid nitrogen. Supernatants were precleared and incubated with EZview Red ANTI-FLAG M2 affinity Gel (Sigma). The beads were removed by spinning and RNA was then extracted using phenol:chloroform. Extracted RNA was processed into sequencing libraries and sequenced at Fasteris (http://www.fasteris.com, Switzerland) using the Illumina MiSeq sequencer Illumina MiSeq gds 302790195 GSM2790195 GEO Accession GSM2790195 SRX3204197 GSM2790196 SRP118529 SRS2530447 GSM2790196 RNA-Seq TRANSCRIPTOMIC cDNA For each sample, ~20 different plates were frozen and ground in liquid nitrogen. Supernatants were precleared and incubated with EZview Red ANTI-FLAG M2 affinity Gel (Sigma). The beads were removed by spinning and RNA was then extracted using phenol:chloroform. Extracted RNA was processed into sequencing libraries and sequenced at Fasteris (http://www.fasteris.com, Switzerland) using the Illumina MiSeq sequencer Illumina MiSeq gds 302790196 GSM2790196 GEO Accession GSM2790196 SRX3204198 GSM2790197 SRP118529 SRS2530448 GSM2790197 RNA-Seq TRANSCRIPTOMIC cDNA For each sample, ~20 different plates were frozen and ground in liquid nitrogen. Supernatants were precleared and incubated with EZview Red ANTI-FLAG M2 affinity Gel (Sigma). The beads were removed by spinning and RNA was then extracted using phenol:chloroform. Extracted RNA was processed into sequencing libraries and sequenced at Fasteris (http://www.fasteris.com, Switzerland) using the Illumina MiSeq sequencer Illumina MiSeq gds 302790197 GSM2790197 GEO Accession GSM2790197 SRX3204199 GSM2790198 SRP118529 SRS2530449 GSM2790198 RNA-Seq TRANSCRIPTOMIC cDNA For each sample, ~20 different plates were frozen and ground in liquid nitrogen. Supernatants were precleared and incubated with EZview Red ANTI-FLAG M2 affinity Gel (Sigma). The beads were removed by spinning and RNA was then extracted using phenol:chloroform. Extracted RNA was processed into sequencing libraries and sequenced at Fasteris (http://www.fasteris.com, Switzerland) using the Illumina MiSeq sequencer Illumina MiSeq gds 302790198 GSM2790198 GEO Accession GSM2790198 SRX3204200 GSM2790199 SRP118529 SRS2530450 GSM2790199 RNA-Seq TRANSCRIPTOMIC cDNA For each sample, ~20 different plates were frozen and ground in liquid nitrogen. Supernatants were precleared and incubated with EZview Red ANTI-FLAG M2 affinity Gel (Sigma). The beads were removed by spinning and RNA was then extracted using phenol:chloroform. Extracted RNA was processed into sequencing libraries and sequenced at Fasteris (http://www.fasteris.com, Switzerland) using the Illumina MiSeq sequencer Illumina MiSeq gds 302790199 GSM2790199 GEO Accession GSM2790199 SRX3204201 GSM2790200 SRP118529 SRS2530451 GSM2790200 RNA-Seq TRANSCRIPTOMIC cDNA For each sample, ~20 different plates were frozen and ground in liquid nitrogen. Supernatants were precleared and incubated with EZview Red ANTI-FLAG M2 affinity Gel (Sigma). The beads were removed by spinning and RNA was then extracted using phenol:chloroform. Extracted RNA was processed into sequencing libraries and sequenced at Fasteris (http://www.fasteris.com, Switzerland) using the Illumina MiSeq sequencer Illumina MiSeq gds 302790200 GSM2790200 GEO Accession GSM2790200 SRX3204202 GSM2790201 SRP118529 SRS2530452 GSM2790201 RNA-Seq TRANSCRIPTOMIC cDNA For each sample, ~20 different plates were frozen and ground in liquid nitrogen. Supernatants were precleared and incubated with EZview Red ANTI-FLAG M2 affinity Gel (Sigma). The beads were removed by spinning and RNA was then extracted using phenol:chloroform. Extracted RNA was processed into sequencing libraries and sequenced at Fasteris (http://www.fasteris.com, Switzerland) using the Illumina MiSeq sequencer Illumina MiSeq gds 302790201 GSM2790201 GEO Accession GSM2790201 SRX3204203 GSM2790202 SRP118529 SRS2530455 GSM2790202 RNA-Seq TRANSCRIPTOMIC cDNA For each sample, ~20 different plates were frozen and ground in liquid nitrogen. Supernatants were precleared and incubated with EZview Red ANTI-FLAG M2 affinity Gel (Sigma). The beads were removed by spinning and RNA was then extracted using phenol:chloroform. Extracted RNA was processed into sequencing libraries and sequenced at Fasteris (http://www.fasteris.com, Switzerland) using the Illumina MiSeq sequencer Illumina MiSeq gds 302790202 GSM2790202 GEO Accession GSM2790202