Hi Kevin,
I'm reading about imputation, but one thing is not clear. Assuming phasing and imputation of genotypes of a given population that is not present in the 1000 reference genome, could you please kindly let me know if just the VCF files generated from whole-genome sequencing of this specific population can be used as the reference (instead of using 1000 genome reference) for phasing and imputation by these tools?
Many thanks for all your help in advance
There is this a recent paper:
Molgenis-impute: imputation pipeline in a box
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4541731/
or a pipeline from github:
https://github.com/CNSGenomics/impute-pipe
Thanks, I'll look into it.
In any case, I would be very grateful if someone could share even just a fake little example with me. I start from .hap .legend and genetic_map* files I retrieve from Impute2 website and then I use my binary plink format files with genotypes as input. I think this is all I need, since I have installed all necessary software.