This image facilitates the usage of MafFilter, a multiple genome alignment files processor.
You should adapt and run the following command: docker run --rm -v /your/data/dir:/data pegi3s/maffilter input.file=/data/mafFile input.file.compression=none input.format=Maf output.log=/data/out_name.log "maf.filter=XFullGap(species=(hg18, panTro1, baboon, mm4, rn3)), Output(file=/data/filtered.maf)"
In this command, you should replace:
/your/data/dir to point to the directory that contains the input file(s).mafFile to the actual name of your MAF alignment file.output/out_name.log to the actual name of your output file.XFullGap(...) to the MafFilter filter(s) you want to apply.filtered.maf to the actual name of your output file.To see the MafFilter help, just run docker run --rm pegi3s/maffilter.
Content type
Image
Digest
sha256:491120dad…
Size
1.3 GB
Last updated
17 days ago
docker pull pegi3s/maffilter