I use this software according to the article, and I got this error:
Extracting reads from S3
skipped 98412 duplicated reads
Aligning reads to IMGT database
processing FASTQ file
found 151748 reads
processing MSA file
found 26381 HLA exons
processing FASTQ file
terminate called after throwing an instance of 'std::bad_alloc'
what(): std::bad_alloc
matched to 0 HLA exons
0 reads matched to HLA types not in the MSA file
translating matches to MSA
Typing
Error in fread(align.path) : File is empty: hla-1c/1c.tsv
Execution halted
Traceback (most recent call last):
File "/opt/bin/run.py", line 64, in
check_call(bin_args)
File "/usr/lib/python2.7/subprocess.py", line 540, in check_call
raise CalledProcessError(retcode, cmd)
subprocess.CalledProcessError: Command '['/opt/bin/typer.sh', 'HLA-1-clean_sorted.bam', '1c']' returned non-zero exit status 1
I use this software according to the article, and I got this error: Extracting reads from S3 skipped 98412 duplicated reads Aligning reads to IMGT database processing FASTQ file found 151748 reads processing MSA file found 26381 HLA exons processing FASTQ file terminate called after throwing an instance of 'std::bad_alloc' what(): std::bad_alloc matched to 0 HLA exons 0 reads matched to HLA types not in the MSA file translating matches to MSA Typing Error in fread(align.path) : File is empty: hla-1c/1c.tsv Execution halted Traceback (most recent call last): File "/opt/bin/run.py", line 64, in
check_call(bin_args)
File "/usr/lib/python2.7/subprocess.py", line 540, in check_call
raise CalledProcessError(retcode, cmd)
subprocess.CalledProcessError: Command '['/opt/bin/typer.sh', 'HLA-1-clean_sorted.bam', '1c']' returned non-zero exit status 1