snakepipes
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Customizable workflows based on snakemake and python for the analysis of NGS data
I dug a bit into the logs and I noticed that even if the data are paired-end MACS2 is not in paired end mode. I am feeding the --peakCallerOptions "-f...
This is the error I encountered: ```bash ChIP-seq -d /mnt/c/AP01/bamSpikes -j 8 --local --useSpikeInForNorm --getSizeFactorsFrom genome --spikeinExt Chromosome --sampleSheet /mnt/c/AP01/bamSpikes/H3K36me3.tsv --windowSize 500 mm10_gencodeM19_spikes /mnt/c/AP01/bamSpikes/H3K36me3_chip_type.yaml mambaforge/envs/snakePipes/lib/python3.11/site-packages/snakePipes/workflows/ChIP-seq/internals.snakefile:71: UserWarning: fragmentSize.metric.tsv is empty, this...
Using -q / --quiet on top of a dryrun would make parsing the proposed number of rules more straight forward and easier to replicate with changing versions of snakemake. (which...
AnnotatedResults_MACS2_sampleSheet/Filtered.results.*_withNearestGene.txt had only 'NA' for GeneID and GeneSymbol. Looks like the wrong columns in the input bed (AnnotatedResults_MACS2_sampleSheet/Filtered.results.*_withNearestTranscript.txt) were used.
Using the following command, I tried running the DNA-mapping pipeline using a customized cluster config yaml to circumvent issues with one node on our server: `DNA-mapping --DAG --trim --trimmerOptions '-a...
- [ ] update outputs, DAGs and folder descriptions for workflows - [ ] section on common options? - [ ] add a cookbook/FAQ section - [ ] update example...
bwa aligned bams aren't properly filtered because of this and just sym-linked
We recently came across the issue where the spikein GTF as specified using createIndices is not considered when using featureCounts in the mRNA-seq pipeline.
currently, `mincount` is hardcoded to 20, which might be too high for some cutNx experiments