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parklab / xTea

Comprehensive TE insertion identification with WGS/WES data from multiple sequencing technics
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Possible to merge TE sites and do genotyping in each sample? #104

Closed dr-ashu-geno closed 4 months ago

dr-ashu-geno commented 5 months ago

Hi.

Thank you for developing xTea.

A short question: any programs you recommend for merging TE sites in all samples and genotype the sites in each sample after merging step? In addition, I have SV data from other programs like Manta, DELLY, etc., do you know how I can merge xTea output with outputs from those programs? (and a program to genotype each sample for list of SVs after merge?).

Thank you in advance,

simoncchu commented 5 months ago

I have this script to merge vcfs to one: https://github.com/parklab/xTea/blob/master/xtea/x_vcf_merger.py, but it's not like the standard "genotyping" module, and just merge the vcfs. You can also do this using other tools like bedtoos/vcftools.

It's not straightforward to merge with Manta/DELLY output, as they also report some TE insertions in their output. I think the easiest way is to write your own scripts.