Comments (3)
Hi David, thank you for the reporting.
What I think weird is this part since it's not possible.
[2017-3-2 15:15:57] 0 from read-pair evidences
What kind of dataset did you use?
Vaquita needs short & paired-end dataset.
eg. The current version does not support long-reads dataset.
hg19.fa must contain all the reference sequences that were used in making .bam files.
Sometimes it can be different. For example, one can consider mitochondrial genome in alignment while your hg19 does not contain it.
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Regarding 2 you can check it like this
shell > samtools view -H input.bam
@hd VN:1.5 SO:coordinate
@sq SN:chr10 LN:135534747
@sq SN:chr11 LN:135006516
@sq SN:chr11_gl000202_random LN:40103
.
.
@sq SN:chrX LN:155270560
@sq SN:chrY LN:59373566
@rg ID:1 LB:lib1 PL:illumina SM:20 PU:unit1
All the name after "SN" should be listed like this.
shell> cat hg19.fa | grep ">"
>chr10
>chr11
>chr11_gl000202_random
.
.
>chrX
>chrY
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Thanks for the super quick reply!
Yeah, the cause of the error is that I used long read data. I didn't catch that Vaquita isn't for long reads just yet. So I will try again with short paired end reads.
Thanks again!
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Related Issues (15)
- Better .vcf outputs.
- Adding test cases
- Connect with Travis for CI HOT 1
- Set user group / mailing lists
- Better packaging
- Build binaries for other OS HOT 1
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- Use new SeqAn library
- Multisample genotpying. HOT 1
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- Don't segfault when no bam index file exists.
- Converting to seqan3
- q
- take too much time to run vaquita
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