Closed akhats closed 7 years ago
Could you provide the command line you used?
I am trying to extract fastq files from one of the bam files of TCGA whole-exome dataset.
bamtofastq \
collate=1 \
exclude=QCFAIL,SECONDARY,SUPPLEMENTARY \
filename= <input.bam> \
gz=1 \
inputformat=bam
level=5 \
outputperreadgroup=1 \
outputperreadgroupsuffixF=_1.fq.gz \
outputperreadgroupsuffixF2=_2.fq.gz \
outputperreadgroupsuffixO=_o1.fq.gz \
outputperreadgroupsuffixO2=_o2.fq.gz \
outputperreadgroupsuffixS=_s.fq.gz \
tryoq=1 \
Assuming you really do have a space after filename= then please retry without, i.e.
bamtofastq filename=in.bam
instead of
bamtofastq filename= in.bam
On 13.03.2017 16:00, akhats wrote:
I am trying to extract fastq files from one of the bam files of TCGA whole-exome dataset.
- I initially tried the command they have mentioned on gdc docs https://docs.gdc.cancer.gov/Data/Bioinformatics_Pipelines/DNA_Seq_Variant_Calling_Pipeline/.
|bamtofastq \ collate=1 \ exclude=QCFAIL,SECONDARY,SUPPLEMENTARY \ filename=
\ gz=1 \ inputformat=bam level=5 \ outputperreadgroup=1 \ outputperreadgroupsuffixF=_1.fq.gz \ outputperreadgroupsuffixF2=_2.fq.gz \ outputperreadgroupsuffixO=_o1.fq.gz \ outputperreadgroupsuffixO2=_o2.fq.gz \ outputperreadgroupsuffixS=_s.fq.gz \ tryoq=1 \ |
- I also tried removing tryoq=1 and level=5 options.
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Ohh, the space!! Thanks 👍 It works now.
Hi there, I tried installing it with
conda install biobimbam
which install version 2.0.62-0. When I run bamtofastq in gives me this error which seems to be related to libmaus2I tried to compile it (version 2.0.70) with libmaus2 as described in README.md but it again throws similar looking error :