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Thank you for your interesting idea!
Actually, I would really love to develop such a module (for a long time), but I know I won't have the time at the moment. I need to completely change the code and integrate a database.
Currently, I would like to add a "barcode" feature, representing the presence/absence of SV (with homozygote/heterozygote status), to search for recurrence between families or group of individuals.
The user will be able to add a list of sorted samples to the configuration file. Then, the barcode will represent the SV’s zygosity status in this ordered list of samples:
Samples homozygotes for the reference allele will be represented using “0”
Heterozygous SV will be represented using “1”
Unknown SV will be represented using "2"
Homozygous variants will be represented with “3”
(like gt_types values from the cyvcf2 Python library).
I let this issue open, so that any user interested in such a development can participate.
Feel free to expand on your needs.
Hi!
Is there the possibility of developing a pipeline for family-based filtering of structural variants?
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