Thanks a lot! Do you mean that I can impute variants with a single sample as long as I use a reference panel in the 'ref=' flag? I wanted to use the Michigan Imputation Server but it tells me it needs at least 50 samples.
Hello,
I am a new user of Beagle and I am trying to use it on a VCF with 1 patient sample. The VCF contains chromosomes 1-22, X and Y. It contains genotype information for all variants, but phasing information is only available for some variants. I wish to impute the phasing information using Beagle.
When I tried running it through Beagle, the following error message showed:
ERROR: there is only one sample
How can I circumvent this error? Can I subset the VCF by chromosome and merge them so that there are many different samples in the same VCF?
1 answer
You cannot impute variants with a single sample and no reference panel. You need to download a reference panel like the 1000 genomes and use that. Alternatively, use an imputation server like the Michigan Imputation Server or Sanger Imputation Server.
You cannot use Michigan Imputation Server. You do need a reference panel.
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phosphorus Wishing You a Happy New Year! Have you managed to address this issue? I'm encountering challenges with phasing a single-sample VCF as well."