Open jgrundstad opened 8 years ago
For now, it is not possible to process insertion/deletion variants.
We are planning to add this feature in a future release, but this might take some time since we want to upgrade the different components to improve performance.
I'm running into an error in the duplicated_snps module:
pyGenClean ERROR] duplicated_snps: ATGCATGC: unknown allele
Is it possible to process datasets that include deletion/insertion variants? Let me know if I can clarify further.
Thanks!