You signed in with another tab or window. Reload to refresh your session.You signed out in another tab or window. Reload to refresh your session.You switched accounts on another tab or window. Reload to refresh your session.Dismiss alert
{{ message }}
This repository has been archived by the owner on Oct 2, 2020. It is now read-only.
At least when running samtools-faidx without docker, the input fasta (.fa) file is replaced with a symlink pointing to itself:
[samuel 002-resequencing]$ ll *fa
lrwxrwxrwx 1 samuel samuel 98 maj 18 20:43 Homo_sapiens.GRCh37.75.dna.chromosome.17.fa -> /home/samuel/code/bils/cwl-evaluation/002-resequencing/Homo_sapiens.GRCh37.75.dna.chromosome.17.fa
The problem is solved (at least for me), when uncommenting the .fai part on line 34 in samtools-faidx.cwl, so as to let samtools faidx only return the newly created .fai file.
The text was updated successfully, but these errors were encountered:
samuell
added a commit
to NBISweden/workflows
that referenced
this issue
May 18, 2016
At least when running samtools-faidx without docker, the input fasta (.fa) file is replaced with a symlink pointing to itself:
The problem is solved (at least for me), when uncommenting the
.fai
part on line 34 in samtools-faidx.cwl, so as to let samtools faidx only return the newly created.fai
file.The text was updated successfully, but these errors were encountered: