any advice on where i can find the genetic map for the GRCh38 version of 1000Genomes? this is needed as a parameter in the imputation process by IMPUTE2.
impute2 is extremely outdated now, its nearly 10 years and and 3 versions have been released since then. Unless there is a very good reason, you should be using impute5 https://journals.plos.org/plosgenetics/article?id=10.1371/journal.pgen.1009049
thanks for the recommendation. the reason behind using IMPUTE2 is the -merge_ref_panels option which is not available in IMPUTE5
why not just merge them using e.g. bcftools before and then run IMPUTE5?
the idea behind the -merge_ref_panels from IMPUTE5 is that it merges one reference panel into the other then use the output for imputation. i am interested to see is one reference panel would be unable to impute the rare variants and hence the impact on the imputation process
i finally found the genetic map for build GRCh38. it is at the below link if anyone needs to have it
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