Hi Jen, Thanks for your reply! I know this workflow. I am just wondering if there is a tool in Galaxy to combine the reads that mapped to the same gene with different positions before running cufflinks. Thanks again, Yan -----邮件原件----- 发件人: Jennifer Jackson [mailto:jen@bx.psu.edu] 发送时间: Wednesday, August 15, 2012 11:01 AM 收件人: Yan He 抄送: galaxy-user@lists.bx.psu.edu 主题: Re: [galaxy-user] how to sort mapped data? Hello Yan, To sort a SAM file produced by Bowtie before using it with Cufflinks (a requirement), please see this FAQ and workflow: http://main.g2.bx.psu.edu/u/jeremy/p/transcriptome-analysis-faq#faq2 Best, Jen Galaxy team On 8/14/12 7:33 PM, Yan He wrote:
Hi everyone,
I am working on RNA-seq data. First, I mapped the reads to the reference transcriptome using bowtie. I found some different reads mapped to the same gene with different positions. Before running Cufflinks, I would like to combine the reads that mapped to the same gene though with different positions. Is there a tool in Galaxy can fulfill this purpose? Any suggestion would be much appreciated. Thanks!
Yan
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