proteomicslfq
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Proteomics label-free quantification (LFQ) analysis pipeline
First try to include XTandem as another search engine.
E.g. different enzymes. Note that e.g. Comet can directly search with a second enzyme. The difficulty is that you usually need to specify if the enzyme was applied after each...
My pipeline fails when using Lys-C as a digestion enzyme, ```NT=Lys-C;AC=MS:1001309 ``` or ```NT=Lys-C/P;AC=MS_1001310```. It works with trypsin ```NT=Trypsin;AC=MS_1001251```. My command is: ``` nextflow run nf-core/proteomicslfq -r 43c77e5 -profile singularity...
Hi, Congratulations for the 1.0.0 release! I'm testing it with a QC HeLa sample but I got some errors. Could you help me? Thanks! ``` nextflow N E X T...
Useful for huge studies where the samples are actually unrelated. Unrelatedness could be one or more of the following: - Different number of fractions - Different instruments - Unrelated conditions...
This would introduce a for-loop around ProteomicsLFQ with the contrasts you actually want to test. That: a) you reduce memory consumption significantly since not all maps are loaded and aligned...
We could also overwrite the experimental design generated from the SDRF but I don't know if that gets even more confusing. Maybe in the long run we even deprecated the...
@jpfeuffer sometimes the pipeline fails in the id part because of the peak-peaking step by the ThermoRawFileParser. Would be great to "restart" the pipeline, same parameters but with the openms...
- Address remaining TODOs. - Adhere to nextflow coding standard by prefixing all channels with ch (required by some code highlighters).