SRX2279720 GSM2363435 SRP092246 SRS1766286 GSM2363435 OTHER TRANSCRIPTOMIC other iCLIP experiments were performed following a published protocol (Konig et al, 2011), with minor modifications (Rodor et al, 2016). The immunoprecipitation (IP) step was carried out using an anti-RBM10 antibody (ab72423, Abcam) that recognizes the two isoforms of the murine RBM10 proteins. Four independent experiments of the RBM10 protocol were performed. The four RBM10 iCLIP libraries with different barcodes were pooled together and sequenced on a single lane by single end sequencing 50nt on an Illumina HiSeq 2000 system (BGI). Equivalent volume of the control libraries was sequenced on a different lane. Illumina HiSeq 2000 gds 302363435 GEO Accession GSM2363435 SRX2279721 GSM2363436 SRP092246 SRS1766287 GSM2363436 OTHER TRANSCRIPTOMIC other iCLIP experiments were performed following a published protocol (Konig et al, 2011), with minor modifications (Rodor et al, 2016). The immunoprecipitation (IP) step was carried out using an anti-RBM10 antibody (ab72423, Abcam) that recognizes the two isoforms of the murine RBM10 proteins. Four independent experiments of the RBM10 protocol were performed. The four RBM10 iCLIP libraries with different barcodes were pooled together and sequenced on a single lane by single end sequencing 50nt on an Illumina HiSeq 2000 system (BGI). Equivalent volume of the control libraries was sequenced on a different lane. Illumina HiSeq 2000 gds 302363436 GEO Accession GSM2363436 SRX2279722 GSM2363437 SRP092246 SRS1766288 GSM2363437 OTHER TRANSCRIPTOMIC other iCLIP experiments were performed following a published protocol (Konig et al, 2011), with minor modifications (Rodor et al, 2016). The immunoprecipitation (IP) step was carried out using an anti-RBM10 antibody (ab72423, Abcam) that recognizes the two isoforms of the murine RBM10 proteins. Four independent experiments of the RBM10 protocol were performed. The four RBM10 iCLIP libraries with different barcodes were pooled together and sequenced on a single lane by single end sequencing 50nt on an Illumina HiSeq 2000 system (BGI). Equivalent volume of the control libraries was sequenced on a different lane. Illumina HiSeq 2000 gds 302363437 GEO Accession GSM2363437 SRX2279723 GSM2363438 SRP092246 SRS1766289 GSM2363438 OTHER TRANSCRIPTOMIC other iCLIP experiments were performed following a published protocol (Konig et al, 2011), with minor modifications (Rodor et al, 2016). The immunoprecipitation (IP) step was carried out using an anti-RBM10 antibody (ab72423, Abcam) that recognizes the two isoforms of the murine RBM10 proteins. Four independent experiments of the RBM10 protocol were performed. The four RBM10 iCLIP libraries with different barcodes were pooled together and sequenced on a single lane by single end sequencing 50nt on an Illumina HiSeq 2000 system (BGI). Equivalent volume of the control libraries was sequenced on a different lane. Illumina HiSeq 2000 gds 302363438 GEO Accession GSM2363438 SRX2279724 GSM2363439 SRP092246 SRS1766290 GSM2363439 OTHER TRANSCRIPTOMIC other iCLIP experiments were performed following a published protocol (Konig et al, 2011), with minor modifications (Rodor et al, 2016). The immunoprecipitation (IP) step was carried out using an anti-RBM10 antibody (ab72423, Abcam) that recognizes the two isoforms of the murine RBM10 proteins. Four independent experiments of the RBM10 protocol were performed. The four RBM10 iCLIP libraries with different barcodes were pooled together and sequenced on a single lane by single end sequencing 50nt on an Illumina HiSeq 2000 system (BGI). Equivalent volume of the control libraries was sequenced on a different lane. Illumina HiSeq 2000 gds 302363439 GEO Accession GSM2363439 SRX2279725 GSM2363440 SRP092246 SRS1766291 GSM2363440 OTHER TRANSCRIPTOMIC other iCLIP experiments were performed following a published protocol (Konig et al, 2011), with minor modifications (Rodor et al, 2016). The immunoprecipitation (IP) step was carried out using an anti-RBM10 antibody (ab72423, Abcam) that recognizes the two isoforms of the murine RBM10 proteins. Four independent experiments of the RBM10 protocol were performed. The four RBM10 iCLIP libraries with different barcodes were pooled together and sequenced on a single lane by single end sequencing 50nt on an Illumina HiSeq 2000 system (BGI). Equivalent volume of the control libraries was sequenced on a different lane. Illumina HiSeq 2000 gds 302363440 GEO Accession GSM2363440 SRX2279726 GSM2363441 SRP092246 SRS1766292 GSM2363441 OTHER TRANSCRIPTOMIC other iCLIP experiments were performed following a published protocol (Konig et al, 2011), with minor modifications (Rodor et al, 2016). The immunoprecipitation (IP) step was carried out using an anti-RBM10 antibody (ab72423, Abcam) that recognizes the two isoforms of the murine RBM10 proteins. Four independent experiments of the RBM10 protocol were performed. The four RBM10 iCLIP libraries with different barcodes were pooled together and sequenced on a single lane by single end sequencing 50nt on an Illumina HiSeq 2000 system (BGI). Equivalent volume of the control libraries was sequenced on a different lane. Illumina HiSeq 2000 gds 302363441 GEO Accession GSM2363441 SRX2279727 GSM2363442 SRP092246 SRS1766293 GSM2363442 OTHER TRANSCRIPTOMIC other iCLIP experiments were performed following a published protocol (Konig et al, 2011), with minor modifications (Rodor et al, 2016). The immunoprecipitation (IP) step was carried out using an anti-RBM10 antibody (ab72423, Abcam) that recognizes the two isoforms of the murine RBM10 proteins. Four independent experiments of the RBM10 protocol were performed. The four RBM10 iCLIP libraries with different barcodes were pooled together and sequenced on a single lane by single end sequencing 50nt on an Illumina HiSeq 2000 system (BGI). Equivalent volume of the control libraries was sequenced on a different lane. Illumina HiSeq 2000 gds 302363442 GEO Accession GSM2363442 SRX2279728 GSM2363443 SRP092246 SRS1766295 GSM2363443 RNA-Seq TRANSCRIPTOMIC cDNA RNA extractions were performed using RNeasy Mini Kit (Qiagen) with DNase treatment on column. The libraries have been obtained using the Truseq Transcriptome kit (polyA transcript enrichment) at the Beijing Genomics Institute (BGI). Illumina HiSeq 2000 gds 302363443 GEO Accession GSM2363443 SRX2279729 GSM2363444 SRP092246 SRS1766294 GSM2363444 RNA-Seq TRANSCRIPTOMIC cDNA RNA extractions were performed using RNeasy Mini Kit (Qiagen) with DNase treatment on column. The libraries have been obtained using the Truseq Transcriptome kit (polyA transcript enrichment) at the Beijing Genomics Institute (BGI). Illumina HiSeq 2000 gds 302363444 GEO Accession GSM2363444 SRX2279730 GSM2363445 SRP092246 SRS1766296 GSM2363445 RNA-Seq TRANSCRIPTOMIC cDNA RNA extractions were performed using RNeasy Mini Kit (Qiagen) with DNase treatment on column. The libraries have been obtained using the Truseq Transcriptome kit (polyA transcript enrichment) at the Beijing Genomics Institute (BGI). Illumina HiSeq 2000 gds 302363445 GEO Accession GSM2363445 SRX2279731 GSM2363446 SRP092246 SRS1766297 GSM2363446 RNA-Seq TRANSCRIPTOMIC cDNA RNA extractions were performed using RNeasy Mini Kit (Qiagen) with DNase treatment on column. The libraries have been obtained using the Truseq Transcriptome kit (polyA transcript enrichment) at the Beijing Genomics Institute (BGI). Illumina HiSeq 2000 gds 302363446 GEO Accession GSM2363446 SRX2279732 GSM2363447 SRP092246 SRS1766298 GSM2363447 RNA-Seq TRANSCRIPTOMIC cDNA RNA extractions were performed using RNeasy Mini Kit (Qiagen) with DNase treatment on column. The libraries have been obtained using the Truseq Transcriptome kit (polyA transcript enrichment) at the Beijing Genomics Institute (BGI). Illumina HiSeq 2000 gds 302363447 GEO Accession GSM2363447 SRX2279733 GSM2363448 SRP092246 SRS1766299 GSM2363448 RNA-Seq TRANSCRIPTOMIC cDNA RNA extractions were performed using RNeasy Mini Kit (Qiagen) with DNase treatment on column. The libraries have been obtained using the Truseq Transcriptome kit (polyA transcript enrichment) at the Beijing Genomics Institute (BGI). Illumina HiSeq 2000 gds 302363448 GEO Accession GSM2363448 SRX2279734 GSM2363449 SRP092246 SRS1766300 GSM2363449 RNA-Seq TRANSCRIPTOMIC cDNA RNA extractions were performed using RNeasy Mini Kit (Qiagen) with DNase treatment on column. The libraries have been obtained using the Truseq Transcriptome kit (polyA transcript enrichment) at the Beijing Genomics Institute (BGI). Illumina HiSeq 2000 gds 302363449 GEO Accession GSM2363449 SRX2279735 GSM2363450 SRP092246 SRS1766301 GSM2363450 RNA-Seq TRANSCRIPTOMIC cDNA RNA extractions were performed using RNeasy Mini Kit (Qiagen) with DNase treatment on column. The libraries have been obtained using the Truseq Transcriptome kit (polyA transcript enrichment) at the Beijing Genomics Institute (BGI). Illumina HiSeq 2000 gds 302363450 GEO Accession GSM2363450 SRX2279736 GSM2363451 SRP092246 SRS1766302 GSM2363451 RNA-Seq TRANSCRIPTOMIC cDNA RNA extractions were performed using RNeasy Mini Kit (Qiagen) with DNase treatment on column. The libraries have been obtained using the Truseq Transcriptome kit (polyA transcript enrichment) at the Beijing Genomics Institute (BGI). Illumina HiSeq 2000 gds 302363451 GEO Accession GSM2363451 SRX2279737 GSM2363452 SRP092246 SRS1766303 GSM2363452 RNA-Seq TRANSCRIPTOMIC cDNA RNA extractions were performed using RNeasy Mini Kit (Qiagen) with DNase treatment on column. The libraries have been obtained using the Truseq Transcriptome kit (polyA transcript enrichment) at the Beijing Genomics Institute (BGI). Illumina HiSeq 2000 gds 302363452 GEO Accession GSM2363452 SRX2279738 GSM2363453 SRP092246 SRS1766304 GSM2363453 RNA-Seq TRANSCRIPTOMIC cDNA RNA extractions were performed using RNeasy Mini Kit (Qiagen) with DNase treatment on column. The libraries have been obtained using the Truseq Transcriptome kit (polyA transcript enrichment) at the Beijing Genomics Institute (BGI). Illumina HiSeq 2000 gds 302363453 GEO Accession GSM2363453 SRX2279739 GSM2363454 SRP092246 SRS1766305 GSM2363454 RNA-Seq TRANSCRIPTOMIC cDNA RNA extractions were performed using RNeasy Mini Kit (Qiagen) with DNase treatment on column. The libraries have been obtained using the Truseq Transcriptome kit (polyA transcript enrichment) at the Beijing Genomics Institute (BGI). Illumina HiSeq 2000 gds 302363454 GEO Accession GSM2363454 SRX2279740 GSM2363455 SRP092246 SRS1766306 GSM2363455 RNA-Seq TRANSCRIPTOMIC cDNA RNA extractions were performed using RNeasy Mini Kit (Qiagen) with DNase treatment on column. The libraries have been obtained using the Truseq Transcriptome kit (polyA transcript enrichment) at the Beijing Genomics Institute (BGI). Illumina HiSeq 2000 gds 302363455 GEO Accession GSM2363455