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Hi there,
Thanks for making the fastqtl tool. I have been trying to test it for some of my data.
I realised that it requires the sample count in the phenotype bed and the genotype vcf to be exactly the same, as shown here:
fastqtl/src/readGenotypes.cpp
Line 55 in 4d03819
and throws an error otherwise.
I was wondering if this could be made slightly more friendly, for example, using only intersecting samples for further analysis.
It is not rare having slightly different numbers of samples in the genotype file and the phenotype file.
Thanks, Zhihao
The text was updated successfully, but these errors were encountered:
Sorry just realised that this is not the official repository. Never mind.
Zhihao
Sorry, something went wrong.
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Hi there,
Thanks for making the fastqtl tool. I have been trying to test it for some of my data.
I realised that it requires the sample count in the phenotype bed and the genotype vcf to be exactly the same, as shown here:
fastqtl/src/readGenotypes.cpp
Line 55 in 4d03819
and throws an error otherwise.
I was wondering if this could be made slightly more friendly, for example, using only intersecting samples for further analysis.
It is not rare having slightly different numbers of samples in the genotype file and the phenotype file.
Thanks,
Zhihao
The text was updated successfully, but these errors were encountered: