SRX3456028 GSM2881275 SRP126359 SRS2744725 GSM2881275 OTHER TRANSCRIPTOMIC other Cell pellets were thawed, lysed with bead beating, and treated with micrococcal nuclease to release single monosomes. Ribosomes were isolated by ultracentrifuging lysate over a sucrose cushion. Ribosome protected fragments (RPF) were extracted from the pelleted ribosomes with miRNeasy RNA Extraction Kit (Qiagen) and size selected between 20 and 35 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881275 GSM2881275 GEO Accession GSM2881275 SRX3456029 GSM2881276 SRP126359 SRS2744726 GSM2881276 OTHER TRANSCRIPTOMIC other Cell pellets were thawed, lysed with bead beating, and treated with micrococcal nuclease to release single monosomes. Ribosomes were isolated by ultracentrifuging lysate over a sucrose cushion. Ribosome protected fragments (RPF) were extracted from the pelleted ribosomes with miRNeasy RNA Extraction Kit (Qiagen) and size selected between 20 and 35 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881276 GSM2881276 GEO Accession GSM2881276 SRX3456030 GSM2881277 SRP126359 SRS2744728 GSM2881277 OTHER TRANSCRIPTOMIC other Cell pellets were thawed, lysed with bead beating, and treated with micrococcal nuclease to release single monosomes. Ribosomes were isolated by ultracentrifuging lysate over a sucrose cushion. Ribosome protected fragments (RPF) were extracted from the pelleted ribosomes with miRNeasy RNA Extraction Kit (Qiagen) and size selected between 20 and 35 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881277 GSM2881277 GEO Accession GSM2881277 SRX3456031 GSM2881278 SRP126359 SRS2744729 GSM2881278 OTHER TRANSCRIPTOMIC other Cell pellets were thawed, lysed with bead beating, and treated with micrococcal nuclease to release single monosomes. Ribosomes were isolated by ultracentrifuging lysate over a sucrose cushion. Ribosome protected fragments (RPF) were extracted from the pelleted ribosomes with miRNeasy RNA Extraction Kit (Qiagen) and size selected between 20 and 35 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881278 GSM2881278 GEO Accession GSM2881278 SRX3456032 GSM2881279 SRP126359 SRS2744727 GSM2881279 OTHER TRANSCRIPTOMIC other Cell pellets were thawed, lysed with bead beating, and treated with micrococcal nuclease to release single monosomes. Ribosomes were isolated by ultracentrifuging lysate over a sucrose cushion. Ribosome protected fragments (RPF) were extracted from the pelleted ribosomes with miRNeasy RNA Extraction Kit (Qiagen) and size selected between 20 and 35 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881279 GSM2881279 GEO Accession GSM2881279 SRX3456033 GSM2881280 SRP126359 SRS2744730 GSM2881280 OTHER TRANSCRIPTOMIC other Cell pellets were thawed, lysed with bead beating, and treated with micrococcal nuclease to release single monosomes. Ribosomes were isolated by ultracentrifuging lysate over a sucrose cushion. Ribosome protected fragments (RPF) were extracted from the pelleted ribosomes with miRNeasy RNA Extraction Kit (Qiagen) and size selected between 20 and 35 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881280 GSM2881280 GEO Accession GSM2881280 SRX3456034 GSM2881281 SRP126359 SRS2744731 GSM2881281 OTHER TRANSCRIPTOMIC other Cell pellets were thawed, lysed with bead beating, and treated with micrococcal nuclease to release single monosomes. Ribosomes were isolated by ultracentrifuging lysate over a sucrose cushion. Ribosome protected fragments (RPF) were extracted from the pelleted ribosomes with miRNeasy RNA Extraction Kit (Qiagen) and size selected between 20 and 35 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881281 GSM2881281 GEO Accession GSM2881281 SRX3456035 GSM2881282 SRP126359 SRS2744732 GSM2881282 OTHER TRANSCRIPTOMIC other Cell pellets were thawed, lysed with bead beating, and treated with micrococcal nuclease to release single monosomes. Ribosomes were isolated by ultracentrifuging lysate over a sucrose cushion. Ribosome protected fragments (RPF) were extracted from the pelleted ribosomes with miRNeasy RNA Extraction Kit (Qiagen) and size selected between 20 and 35 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881282 GSM2881282 GEO Accession GSM2881282 SRX3456036 GSM2881283 SRP126359 SRS2744733 GSM2881283 OTHER TRANSCRIPTOMIC other Cell pellets were thawed and lysed with bead beating. Total RNA was extracted with miRNeasy RNA Extraction Kit (Qiagen). rRNA was subtracted with the Ribozero Gram Negative Kit (Illumina). RNA was then fragmented with heat and alkalinity and size selected between 20 and 40 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881283 GSM2881283 GEO Accession GSM2881283 SRX3456037 GSM2881284 SRP126359 SRS2744734 GSM2881284 OTHER TRANSCRIPTOMIC other Cell pellets were thawed and lysed with bead beating. Total RNA was extracted with miRNeasy RNA Extraction Kit (Qiagen). rRNA was subtracted with the Ribozero Gram Negative Kit (Illumina). RNA was then fragmented with heat and alkalinity and size selected between 20 and 40 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881284 GSM2881284 GEO Accession GSM2881284 SRX3456038 GSM2881285 SRP126359 SRS2744735 GSM2881285 OTHER TRANSCRIPTOMIC other Cell pellets were thawed and lysed with bead beating. Total RNA was extracted with miRNeasy RNA Extraction Kit (Qiagen). rRNA was subtracted with the Ribozero Gram Negative Kit (Illumina). RNA was then fragmented with heat and alkalinity and size selected between 20 and 40 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881285 GSM2881285 GEO Accession GSM2881285 SRX3456039 GSM2881286 SRP126359 SRS2744736 GSM2881286 OTHER TRANSCRIPTOMIC other Cell pellets were thawed and lysed with bead beating. Total RNA was extracted with miRNeasy RNA Extraction Kit (Qiagen). rRNA was subtracted with the Ribozero Gram Negative Kit (Illumina). RNA was then fragmented with heat and alkalinity and size selected between 20 and 40 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881286 GSM2881286 GEO Accession GSM2881286 SRX3456040 GSM2881287 SRP126359 SRS2744737 GSM2881287 OTHER TRANSCRIPTOMIC other Cell pellets were thawed and lysed with bead beating. Total RNA was extracted with miRNeasy RNA Extraction Kit (Qiagen). rRNA was subtracted with the Ribozero Gram Negative Kit (Illumina). RNA was then fragmented with heat and alkalinity and size selected between 20 and 40 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881287 GSM2881287 GEO Accession GSM2881287 SRX3456041 GSM2881288 SRP126359 SRS2744738 GSM2881288 OTHER TRANSCRIPTOMIC other Cell pellets were thawed and lysed with bead beating. Total RNA was extracted with miRNeasy RNA Extraction Kit (Qiagen). rRNA was subtracted with the Ribozero Gram Negative Kit (Illumina). RNA was then fragmented with heat and alkalinity and size selected between 20 and 40 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881288 GSM2881288 GEO Accession GSM2881288 SRX3456042 GSM2881289 SRP126359 SRS2744739 GSM2881289 OTHER TRANSCRIPTOMIC other Cell pellets were thawed and lysed with bead beating. Total RNA was extracted with miRNeasy RNA Extraction Kit (Qiagen). rRNA was subtracted with the Ribozero Gram Negative Kit (Illumina). RNA was then fragmented with heat and alkalinity and size selected between 20 and 40 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881289 GSM2881289 GEO Accession GSM2881289 SRX3456043 GSM2881290 SRP126359 SRS2744741 GSM2881290 OTHER TRANSCRIPTOMIC other Cell pellets were thawed and lysed with bead beating. Total RNA was extracted with miRNeasy RNA Extraction Kit (Qiagen). rRNA was subtracted with the Ribozero Gram Negative Kit (Illumina). RNA was then fragmented with heat and alkalinity and size selected between 20 and 40 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881290 GSM2881290 GEO Accession GSM2881290 SRX3456044 GSM2881291 SRP126359 SRS2744740 GSM2881291 OTHER TRANSCRIPTOMIC other Cell pellets were thawed, lysed with bead beating, and treated with micrococcal nuclease to release single monosomes. Ribosomes were isolated by ultracentrifuging lysate over a sucrose cushion. Ribosome protected fragments (RPF) were extracted from the pelleted ribosomes with miRNeasy RNA Extraction Kit (Qiagen) and size selected between 20 and 35 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881291 GSM2881291 GEO Accession GSM2881291 SRX3456045 GSM2881292 SRP126359 SRS2744742 GSM2881292 OTHER TRANSCRIPTOMIC other Cell pellets were thawed, lysed with bead beating, and treated with micrococcal nuclease to release single monosomes. Ribosomes were isolated by ultracentrifuging lysate over a sucrose cushion. Ribosome protected fragments (RPF) were extracted from the pelleted ribosomes with miRNeasy RNA Extraction Kit (Qiagen) and size selected between 20 and 35 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881292 GSM2881292 GEO Accession GSM2881292 SRX3456046 GSM2881293 SRP126359 SRS2744743 GSM2881293 OTHER TRANSCRIPTOMIC other Cell pellets were thawed, lysed with bead beating, and treated with micrococcal nuclease to release single monosomes. Ribosomes were isolated by ultracentrifuging lysate over a sucrose cushion. Ribosome protected fragments (RPF) were extracted from the pelleted ribosomes with miRNeasy RNA Extraction Kit (Qiagen) and size selected between 20 and 35 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881293 GSM2881293 GEO Accession GSM2881293 SRX3456047 GSM2881294 SRP126359 SRS2744744 GSM2881294 OTHER TRANSCRIPTOMIC other Cell pellets were thawed, lysed with bead beating, and treated with micrococcal nuclease to release single monosomes. Ribosomes were isolated by ultracentrifuging lysate over a sucrose cushion. Ribosome protected fragments (RPF) were extracted from the pelleted ribosomes with miRNeasy RNA Extraction Kit (Qiagen) and size selected between 20 and 35 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881294 GSM2881294 GEO Accession GSM2881294 SRX3456048 GSM2881295 SRP126359 SRS2744745 GSM2881295 OTHER TRANSCRIPTOMIC other Cell pellets were thawed, lysed with bead beating, and treated with micrococcal nuclease to release single monosomes. Ribosomes were isolated by ultracentrifuging lysate over a sucrose cushion. Ribosome protected fragments (RPF) were extracted from the pelleted ribosomes with miRNeasy RNA Extraction Kit (Qiagen) and size selected between 20 and 35 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881295 GSM2881295 GEO Accession GSM2881295 SRX3456049 GSM2881296 SRP126359 SRS2744746 GSM2881296 OTHER TRANSCRIPTOMIC other Cell pellets were thawed, lysed with bead beating, and treated with micrococcal nuclease to release single monosomes. Ribosomes were isolated by ultracentrifuging lysate over a sucrose cushion. Ribosome protected fragments (RPF) were extracted from the pelleted ribosomes with miRNeasy RNA Extraction Kit (Qiagen) and size selected between 20 and 35 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881296 GSM2881296 GEO Accession GSM2881296 SRX3456050 GSM2881297 SRP126359 SRS2744747 GSM2881297 OTHER TRANSCRIPTOMIC other Cell pellets were thawed, lysed with bead beating, and treated with micrococcal nuclease to release single monosomes. Ribosomes were isolated by ultracentrifuging lysate over a sucrose cushion. Ribosome protected fragments (RPF) were extracted from the pelleted ribosomes with miRNeasy RNA Extraction Kit (Qiagen) and size selected between 20 and 35 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881297 GSM2881297 GEO Accession GSM2881297 SRX3456051 GSM2881298 SRP126359 SRS2744748 GSM2881298 OTHER TRANSCRIPTOMIC other Cell pellets were thawed, lysed with bead beating, and treated with micrococcal nuclease to release single monosomes. Ribosomes were isolated by ultracentrifuging lysate over a sucrose cushion. Ribosome protected fragments (RPF) were extracted from the pelleted ribosomes with miRNeasy RNA Extraction Kit (Qiagen) and size selected between 20 and 35 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881298 GSM2881298 GEO Accession GSM2881298 SRX3456052 GSM2881299 SRP126359 SRS2744751 GSM2881299 OTHER TRANSCRIPTOMIC other Cell pellets were thawed and lysed with bead beating. Total RNA was extracted with miRNeasy RNA Extraction Kit (Qiagen). rRNA was subtracted with the Ribozero Gram Negative Kit (Illumina). RNA was then fragmented with heat and alkalinity and size selected between 20 and 40 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881299 GSM2881299 GEO Accession GSM2881299 SRX3456053 GSM2881300 SRP126359 SRS2744750 GSM2881300 OTHER TRANSCRIPTOMIC other Cell pellets were thawed and lysed with bead beating. Total RNA was extracted with miRNeasy RNA Extraction Kit (Qiagen). rRNA was subtracted with the Ribozero Gram Negative Kit (Illumina). RNA was then fragmented with heat and alkalinity and size selected between 20 and 40 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881300 GSM2881300 GEO Accession GSM2881300 SRX3456054 GSM2881301 SRP126359 SRS2744752 GSM2881301 OTHER TRANSCRIPTOMIC other Cell pellets were thawed and lysed with bead beating. Total RNA was extracted with miRNeasy RNA Extraction Kit (Qiagen). rRNA was subtracted with the Ribozero Gram Negative Kit (Illumina). RNA was then fragmented with heat and alkalinity and size selected between 20 and 40 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881301 GSM2881301 GEO Accession GSM2881301 SRX3456055 GSM2881302 SRP126359 SRS2744753 GSM2881302 OTHER TRANSCRIPTOMIC other Cell pellets were thawed and lysed with bead beating. Total RNA was extracted with miRNeasy RNA Extraction Kit (Qiagen). rRNA was subtracted with the Ribozero Gram Negative Kit (Illumina). RNA was then fragmented with heat and alkalinity and size selected between 20 and 40 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881302 GSM2881302 GEO Accession GSM2881302 SRX3456056 GSM2881303 SRP126359 SRS2744754 GSM2881303 OTHER TRANSCRIPTOMIC other Cell pellets were thawed and lysed with bead beating. Total RNA was extracted with miRNeasy RNA Extraction Kit (Qiagen). rRNA was subtracted with the Ribozero Gram Negative Kit (Illumina). RNA was then fragmented with heat and alkalinity and size selected between 20 and 40 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881303 GSM2881303 GEO Accession GSM2881303 SRX3456057 GSM2881304 SRP126359 SRS2744755 GSM2881304 OTHER TRANSCRIPTOMIC other Cell pellets were thawed and lysed with bead beating. Total RNA was extracted with miRNeasy RNA Extraction Kit (Qiagen). rRNA was subtracted with the Ribozero Gram Negative Kit (Illumina). RNA was then fragmented with heat and alkalinity and size selected between 20 and 40 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881304 GSM2881304 GEO Accession GSM2881304 SRX3456058 GSM2881305 SRP126359 SRS2744756 GSM2881305 OTHER TRANSCRIPTOMIC other Cell pellets were thawed and lysed with bead beating. Total RNA was extracted with miRNeasy RNA Extraction Kit (Qiagen). rRNA was subtracted with the Ribozero Gram Negative Kit (Illumina). RNA was then fragmented with heat and alkalinity and size selected between 20 and 40 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881305 GSM2881305 GEO Accession GSM2881305 SRX3456059 GSM2881306 SRP126359 SRS2744830 GSM2881306 OTHER TRANSCRIPTOMIC other Cell pellets were thawed and lysed with bead beating. Total RNA was extracted with miRNeasy RNA Extraction Kit (Qiagen). rRNA was subtracted with the Ribozero Gram Negative Kit (Illumina). RNA was then fragmented with heat and alkalinity and size selected between 20 and 40 bases with denaturing PAGE. RNA samples were ligated to a 3' adaptor and reverse transcribed. The cDNA was circularized to add a 5' adaptor then PCR amplified to add sample specific barcodes. Illumina HiSeq 2000 gds 302881306 GSM2881306 GEO Accession GSM2881306