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I'm trying to use this tool for WGS data on C. elegans so I'm using the -m wgs flag. Furthermore, I have no normal samples to use for the reference so I use the -n flag without specifying any additional BAM files but I'm getting an error:
[moldach@cdr767 first_batch]$ cnvkit.py batch N2_trim_bwaMEM_sort_dedupped.bam -n -m wgs -f /scratch/moldach/data/references/c_elegans.PRJNA13758.WS265.genomic.fa --annotate refFlat.txt
CNVkit 0.9.7.b1
I: Scanning for accessible regions
Accessible region I:0-15072434 (size 15072434)
II: Scanning for accessible regions
Accessible region II:0-15279421 (size 15279421)
III: Scanning for accessible regions
Accessible region III:0-13783801 (size 13783801)
IV: Scanning for accessible regions
Accessible region IV:0-17493829 (size 17493829)
V: Scanning for accessible regions
Accessible region V:0-20924180 (size 20924180)
X: Scanning for accessible regions
Accessible region X:0-17718942 (size 17718942)
MtDNA: Scanning for accessible regions
Accessible region MtDNA:0-13794 (size 13794)
I: Joining over small gaps
II: Joining over small gaps
III: Joining over small gaps
IV: Joining over small gaps
V: Joining over small gaps
X: Joining over small gaps
MtDNA: Joining over small gaps
Wrote c_elegans.PRJNA13758.WS265.genomic.bed with 7 regions
Detected file format: bed
Splitting large targets
Applying annotations as target names
Traceback (most recent call last):
File "/scratch/moldach/bin/cnvkit/.venv/bin/cnvkit.py", line 7, in <module>
exec(compile(f.read(), __file__, 'exec'))
File "/scratch/moldach/bin/cnvkit/cnvkit.py", line 9, in <module>
args.func(args)
File "/scratch/moldach/bin/cnvkit/cnvlib/commands.py", line 110, in _cmd_batch
args.reference, args.targets, args.antitargets = batch.batch_make_reference(
File "/scratch/moldach/bin/cnvkit/cnvlib/batch.py", line 89, in batch_make_reference
target_arr = target.do_target(bait_arr, annotate, short_names, True,
File "/scratch/moldach/bin/cnvkit/cnvlib/target.py", line 20, in do_target
annotation = tabio.read_auto(annotate)
File "/scratch/moldach/bin/cnvkit/skgenome/tabio/__init__.py", line 102, in read_auto
fmt = sniff_region_format(infile)
File "/scratch/moldach/bin/cnvkit/skgenome/tabio/__init__.py", line 224, in sniff_region_format
with as_handle(infile, 'rU') as handle:
File "/cvmfs/soft.computecanada.ca/easybuild/software/2017/Core/python/3.8.0/lib/python3.8/contextlib.py", line 113, in __enter__
return next(self.gen)
File "/scratch/moldach/bin/cnvkit/.venv/lib/python3.8/site-packages/Bio/File.py", line 120, in as_handle
with open(handleish, mode, **kwargs) as fp:
FileNotFoundError: [Errno 2] No such file or directory: 'refFlat.txt'
I thought this command should create the "flat"reference for me? What's going on here?
The text was updated successfully, but these errors were encountered:
It should work if you leave off the --annotate refFlat.txt part. The --annotate option is for providing gene labels, and the argument is a tabular file downloaded from the UCSC Genome Browser FTP site (or another annotation source, as long as it's in GFF, UCSC BED, or UCSC RefGene format.)
I'm trying to use this tool for WGS data on C. elegans so I'm using the
-m wgs
flag. Furthermore, I have no normal samples to use for the reference so I use the-n
flag without specifying any additional BAM files but I'm getting an error:I thought this command should create the "flat"reference for me? What's going on here?
The text was updated successfully, but these errors were encountered: