Comments (2)
Hello @Alteroldis,
This is a very interesting question.
cuteSV can identify the breakend which enrolled in two different chromosomes or different haplotypes of homologous chromosomes. Also, cuteSV can report the read ID that supports the breakend event. So I guess cuteSV can help your purpose in this circumstance. You can use minimap2 to align long-reads to the diploid genome, and then run cuteSV.
Best,
Tao
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Dear Dr Jiang, thank you for quick answer.
I think it makes sense to remove reads that give exactly translocation events, and use the remaining ones for assembly. But, since I have both haplotypes in the assembly and it is unknown which two contigs belong to homologous chromosomes, a problem arises. Let's say reads 1-10 support translocations between contigs A and B. Then there will be another translocation event between contigs B and A with reads 11-21. Is everything correct? By deleting reads 1-21, I will lose part of the genome.
And it seemed strange to me that there was a huge translocation event in the logs, but only about 2000 remained in vcf. Perhaps itβs worth tweaking some settings?
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Related Issues (20)
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