Closed xingwu2 closed 2 months ago
OK, I have found a way to bypass the error. The names of the RNAseq files have to follow this
/([A-Za-z0-9]+).{1,2}$/
according to the bin/egapx/nf/./subworkflows/ncbi/./rnaseq_short/star_wnode/main.nf.
That means there is no special character allowed in the file names and they must end in .1 or .2.
Sorry that I encountered another issue with my local RNAseq read files.
Caused by:
Process `egapx:rnaseq_collapse:run_rnaseq_collapse (3)` terminated with an error exit status (3)
Command error:
00398/018/0054/RE FDC3018E691B8D21 0301/0018 2024-07-12T23:14:36.877003 bse-2021-001.bsehpc.carnegiescience.edu UNK_CLIENT UNK_SESSION rnaseq_collapse request-stop 500 4.473060131 0 40
00398/007/0051/R FDC3018E691B8D21 0302/0009 2024-07-12T23:14:36.890048 bse-2021-001.bsehpc.carnegiescience.edu UNK_CLIENT UNK_SESSION rnaseq_collapse extra num_skipped=359328
00398/007/0051/R FDC3018E691B8D21 0303/0010 2024-07-12T23:14:36.890279 bse-2021-001.bsehpc.carnegiescience.edu UNK_CLIENT UNK_SESSION rnaseq_collapse Error: RNASEQ(CException::eUnknown) "collapse_group.cpp", line 167: SMemberAlignment::SMemberAlignment() --- Failed to get redundant counts from SRA alignment
Hi, We're working on a new release which will be out in a couple weeks. That should take care of these issues. Thank you for reporting.
Pooja
Hi @xingwu2, A new version is out. Please give it a try! Pooja
Hi,
I am trying out the egapx for a genome that is not hosted on NCBI. I have all the required inputs (genome fasta, RNAseq reads in fastq, and protein sequences in fasta from related species). I wonder does egapx work with local files?
This is the error I got from the program.
Attached is my yaml file.
Xing
Ca.yaml.txt