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Error: Type checker found wrong number of fields while tokenizing data line (while building reference) #167
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@sheilazuniga What is your OS environment? Have you tried to re-compile the irfinder core? |
Thanks for your answer, I'm user of cluster: |
@sheilazuniga The conda package is maintained by a third party so I don't know how it is built. The only suggestion I can provide here is to download the GitHub version and try to recompile according to the wiki page. |
Hi @dg520 In v1.3.1:
I got this output information:
The output directory is like following. It seems to run successfully?
In v1.2.6
I got this output information:
The output directory is like following.
My OS information:
What can i do to fix it? Can I quantify IR with this reference? Thanks |
@yangjywhu Is this extra TAB problem due to the version of Bedtools you used? I have never seen this before, so I cannot judge whether your reference has been successfully prepared or not. I would suggest you to update your Bedtools or try a clean installation of Bedtools v2.30.0 (make sure the new Bedtools is set to the default one to be called). |
Hi,
I'm not sure why this is happening, I call:
IRFinder -m BuildRefFromSTARRef -r /my_dir/GRCh38/irfinder/ -x /my_dir/GRCh38/genome-index_STAR -e /my_dir/GRCh38/extra-input-files-IRFinder/RNA.SpikeIn.ERCC.fasta.gz -b /my_dir/GRCh38/extra-input-files-IRFinder/Human_hg38_nonPolyA_ROI.bed
I got: merging from 64 files and 64 in-memory blocks...
Error: Type checker found wrong number of fields while tokenizing data line.
Perhaps you have extra TAB at the end of your line? Check with "cat -t"
Error: Type checker found wrong number of fields while tokenizing data line.
Perhaps you have extra TAB at the end of your line? Check with "cat -t"
The output file containts the following content:
Launching reference build process. The full build might take hours.
<Phase 1: STAR Reference Preparation>
Oct 27 17:01:21 ... copying the genome FASTA file...
Oct 27 17:01:37 ... copying the transcriptome GTF file...
Oct 27 17:01:42 ... copying the STAR reference folder...
<Phase 2: Mapability Calculation>
Oct 27 17:03:11 ... mapping genome fragments back to genome...
Oct 27 17:29:03 ... sorting aligned genome fragments...
Oct 27 17:35:40 ... indexing aligned genome fragments...
Oct 27 17:36:02 ... filtering aligned genome fragments by chromosome/scaffold...
Oct 27 17:39:12 ... merging filtered genome fragments...
Oct 27 17:39:57 ... calculating regions for exclusion...
Oct 27 17:45:01 ... cleaning temporary files...
<Phase 3: IRFinder Reference Preparation>
Oct 27 17:45:03 ... building Ref 1...
Oct 27 17:45:21 ... building Ref 2...
Oct 27 17:45:23 ... building Ref 3...
Oct 27 17:45:23 ... building Ref 4...
Oct 27 17:45:29 ... building Ref 5...
Oct 27 17:45:39 ... building Ref 6...
Oct 27 17:45:39 ... building Ref 7...
Oct 27 17:45:41 ... building Ref 8...
Oct 27 17:45:41 ... building Ref 9...
Oct 27 17:45:41 ... building Ref 10c...
Oct 27 17:45:41 ... building Ref 11c...
And when I enter in the directory
-rw-r--r-- 1 szm group 5.2K Oct 27 17:45 ref-ROI.bed
-rw-r--r-- 1 szm group 0 Oct 27 17:45 intergenic.ROI.bed
-rw-r--r-- 1 szm group 81M Oct 27 17:45 ref-cover.bed
-rw-r--r-- 1 szm group 5.8M Oct 27 17:45 ref-sj.ref
-rw-r--r-- 1 szm group 6.5M Oct 27 17:45 ref-read-continues.ref
-rw-r--r-- 1 szm group 31M Oct 27 17:45 exclude.omnidirectional.bed
-rw-r--r-- 1 szm group 22M Oct 27 17:45 exclude.directional.bed
-rw-r--r-- 1 szm group 13M Oct 27 17:45 introns.unique.bed
Could you please help me?
Thank you in advance,
Sheila
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