Published March 4, 2022
| Version v0.7.2
Software
Open
seq2science
Authors/Creators
- 1. Radboud University
Description
Automated preprocessing of Next-Generation Sequencing data, including full (sc)ATAC-seq, ChIP-seq, and (sc)RNA-seq workflows.
Added- TPM to gene counts conversion with pytxi
- by default attempts to use the GTF file to convert transcript_ids to gene_names
- otherwise will use MyGene.info
- config option
tpm2countsto chose which TPM to counts converter to use
- pytxi is now the default TPM to gene counts converter (over tximeta)
- peak/gene counts tables now use descriptive names (if given)
- MultiQC DESeq2 correlation plots now display correlation metrics in the figure
- using awful practices to eliminate checkpoint strandedness
- deeptools_flags renamed to deeptools_bamcoverage
- rna-seq trackhub per base tracks by default instead of bins per 50
- edge-cases where seq2science was too strict with rerunning
- assembly stats log scale on the y-axis
- s2s explain wont tell you about subsampling to -1 (all) reads
- tn5 shift cigar string parsing edge-case (reference deletions/insertions)
Files
vanheeringen-lab/seq2science-v0.7.2.zip
Files
(21.9 MB)
| Name | Size | Download all |
|---|---|---|
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md5:74777eb844ff94c5fec7d2759c62588e
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21.9 MB | Preview Download |
Additional details
Related works
- Is supplement to
- https://github.com/vanheeringen-lab/seq2science/tree/v0.7.2 (URL)