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Hi, Thanks for developing the pipeline to detect the SV. I got some error when I run the speedseq sv pipeline
[E::bgzf_read] Read block operation failed with error 33 after 0 of 4 bytes
Traceback (most recent call last):
File "/home/taoyan/miniconda3/envs/speedseq/speedseq//bin/svtyper", line 1806, in <module>
sys.exit(main())
File "/home/taoyan/miniconda3/envs/speedseq/speedseq//bin/svtyper", line 1801, in main
args.max_reads)
File "/home/taoyan/miniconda3/envs/speedseq/speedseq//bin/svtyper", line 1532, in sv_genotype
read_batch, many = gather_reads(sample, chromB, posB, ciB, z, read_batch, max_reads)
File "/home/taoyan/miniconda3/envs/speedseq/speedseq//bin/svtyper", line 1315, in gather_reads
min(pos + ci[1] + fetch_flank, chrom_length))):
File "pysam/libcalignmentfile.pyx", line 2094, in pysam.libcalignmentfile.IteratorRowRegion.__next__
IOError: truncated file
The text was updated successfully, but these errors were encountered:
Hi, Thanks for developing the pipeline to detect the SV. I got some error when I run the speedseq sv pipeline
The text was updated successfully, but these errors were encountered: