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I made a draft for a new tutorial for RNAseq data. It uses reads from a TEX-treated sample in V. Cholerae and computes putative transcription start sites in it. It shows how to
download reads from SRA
align reads using bwa-mem
read .bam files and .gff files
annotate alignments with features from .gff files
compute coverage from alignments
compute maxima in the difference along the coverage as putative TSS
Go ahead an make a PR and we can discuss there. When you push to your fork, there should be a button that says "open pull request," but if not, you can open the pull requests tab here or on your repo, click "new PR", and then have your branch target main here:
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maltesie commentedon Apr 16, 2023
I made a draft for a new tutorial for RNAseq data. It uses reads from a TEX-treated sample in V. Cholerae and computes putative transcription start sites in it. It shows how to
Does that make sense? I put everything here
kescobo commentedon Apr 17, 2023
Go ahead an make a PR and we can discuss there. When you push to your fork, there should be a button that says "open pull request," but if not, you can open the pull requests tab here or on your repo, click "new PR", and then have your branch target
mainhere:kescobo commentedon Apr 18, 2023
(if you'd like, I can kick off the PR from your fork, but it's good practice :-) )
maltesie commentedon Apr 18, 2023
I created a PR, I think. Thanks for all the help :)