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View Code? Open in Web Editor NEWA bioinformatics tool for SV detection and virus integration discovery
License: Apache License 2.0
A bioinformatics tool for SV detection and virus integration discovery
License: Apache License 2.0
Hi, I'm running into errors in the seeksv getsv step.
When running "seeksv getsv sample.clip.bam $file sample.clip.gz sample.sv.txt sample.unmapped.clip.fq.gz" it gives:
'InputSoftInfoStoreBreakpoint' finished
Bam/sam sample.bam Mean insert size : 182
Mean deviation: 71
'CalculateInsertsizeDeviation' finished
[bam_index_load] fail to load BAM index.
[main_samview] random alignment retrieval only works for indexed BAM files.
My orignal bam file is indexed, and I've also tried to index the generated sample.clip.bam but this did not help.
Any ideas?
Best,
Hi, thanks for the tool - looking forward to using it. It seems seeksv is using the full sequence as the sequence header/name in the getclip stage, and samtools is choking on this when aligning with bwa (i've tried samtools v1.5 and 1.8):
[M::mem_process_seqs] Processed 161232 reads in 3.408 CPU sec, 3.115 real sec
[E::sam_parse1] query name too long
[W::sam_read1] Parse error at line 235
[main_samview] truncated file.
viewing a sam file gives the same issue:
samtools view -c 14140.clip.sam
[E::sam_parse1] query name too long
[W::sam_read1] Parse error at line 235
[main_samview] truncated file.
example read from clip.fq.gz
@AGGCAATATAAAGATTGCTTTCAATAACCAAGAAGAATTAAACAGAATTATCAACACTCTAAAATAAGGGTGTTGATTATTTTTTTATTTAATCAAACTTATCCACAAGGTATTTTGCTATTTTTCTGTTGATTCTCTAAGCTTTTCTAATTTCCACAGTCTGTGGAAAACTTT
AGGCAATATAAAGATTGCTTTCAATAACCAAGAAGAATTAAACAGAATTATCAACACTCTAAAATAAGGGTGTTGATTATTTTTTTATTTAATCAAACTTATCCACAAGGTATTTTGCTATTTTTCTGTTGATTCTCTAAGCTTTTCTAATTTCCACAGTCTGTGGAAAACTTT
+
+;,+CGCFCFFF<F9=6FCCCCGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
Any suggestions? Thank you
Hi,
is it possible to run seeksv with multiple threads?
I could not find this option in the help and in the online material. I am running a job for an RNA-seq experiment with 30M reads and is taking more than 2 days for the getsv part. Is it normal?
Thanks in advance
it seems seeksv generates more somatic SVs than other callers - do you have any suggestion for applying filtering? thanks
I have get the Final SV output named output.sv.txt
, while I can't find the file format Description.
Some columns of output.sv.txt
is easy to enderstand by its name, some are not. Please add this file format description. Thanks.
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