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Thread | Thread Starter | Forum | Replies | Last Post |
how to calculate the mean sequencing depth of RNA-seq | wangli | RNA Sequencing | 3 | 02-19-2014 05:44 PM |
RNA-seq sequencing depth | NicoBxl | RNA Sequencing | 4 | 02-19-2014 03:48 PM |
Displaying RNA-Seq reads scaled in proportion to the depth of sequencing? | mudpud | RNA Sequencing | 1 | 04-10-2013 03:34 PM |
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#1 |
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Location: https://www.researchgate.net/profile/Woody_Lin Join Date: Jan 2010
Posts: 52
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Greetings,
Does anyone know the number of reads per sample in TCGA RNA-Seq data? Any cancer type will do. Approximate 20 million reads per sample? Woody |
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#2 |
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Location: East Coast USA Join Date: Feb 2008
Posts: 7,089
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TCGA RNA-seq data (submitted by UNC) sequenced on HiSeq typically has between 60M - 150M reads per sample.
Last edited by GenoMax; 02-19-2014 at 01:13 PM. |
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#3 |
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Location: https://www.researchgate.net/profile/Woody_Lin Join Date: Jan 2010
Posts: 52
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Hi GenoMax,
Thanks for the reply. Did you mean 60M to 150M pair-end reads per samples? I assume that most of the TCGA samples don't have this much sequencing depth because some of samples were sequenced before HiSeq became popular. But, I might be out-dated with the information. If most of the TCGA samples have 60M to 150M pair-end reads, that would be nice. Sincerely, Woody |
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#4 |
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Location: East Coast USA Join Date: Feb 2008
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The read number is reflective of the way Illumina counts reads (30M clusters = 60M PE Reads) and is only for samples sequenced on HiSeq.
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#5 |
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Location: https://www.researchgate.net/profile/Woody_Lin Join Date: Jan 2010
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Hi GenoMax,
Thanks for the reply. In other words, that's equal to 30M to 75M "read pairs". Am I right? Bests, Woody |
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