Closed Shinichiro03 closed 2 years ago
Hi Shin,
That is expected, the final GeneTagged bam file contains both the exon and intron gene information derived from featureCounts:
https://github.com/sdparekh/zUMIs/wiki/Output#explanation-of-the-bam-tags-zumis-uses
Best, Christoph
Hi Christoph,
Thank you for your reply. Should I use .filtered.Aligned.GeneTagged.sorted.bam for running ss3iso? This is because ss3iso option part mention that "Use 'filtered.tagged.Aligned.out.bam.ex.featureCounts.UBfix.sort.bam' generated by zUMIs. Every read should have a UB:Z tag.”
Best, Shin
Hi Shin,
yes this is the appropriate bam file. since it seems this is smartseq3 data, I do strongly recommend to use the UMI error correction in zUMIs. In case of issues or doubt with other scripts like ss3iso please refer to those GitHub repositories.
Best Christoph
Hi Christoph,
Thank you very much for your help!
Best, Shin
Hi Christoph,
Thank you for your reply. Should I use .filtered.Aligned.GeneTagged.sorted.bam for running ss3iso? This is because ss3iso option part mention that "Use 'filtered.tagged.Aligned.out.bam.ex.featureCounts.UBfix.sort.bam' generated by zUMIs. Every read should have a UB:Z tag.”
Best, Shin
On Jun 23, 2022, at 2:46 AM, cziegenhain @.***> wrote:
Hi Shin,
That is expected, the final GeneTagged bam file contains both the exon and intron gene information derived from featureCounts:
https://github.com/sdparekh/zUMIs/wiki/Output#explanation-of-the-bam-tags-zumis-uses https://github.com/sdparekh/zUMIs/wiki/Output#explanation-of-the-bam-tags-zumis-uses Best, Christoph
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Sounds correct, yes!
I run example data. In my output directory, I can .filtered.Aligned.GeneTagged.sorted.bam, but without any featureCounts.bam such as .aligned.sorted.bam.featureCounts .ex.featureCounts and .in.featureCounts. I saw those files in /.temp directory, and can not see any error in the terminal.
Could you please tell me how to solve this issue? Really appreciate any of your suggestions and help. Best, Shin