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Post by jgoudet on Jul 16, 2019 22:29:11 GMT
Hi all, I am trying to run an asociation test, and have been successful previously, but I encounter the following with one of my simulated data set:
Analysis started at 16:30:46 UTC on Tue Jul 16 2019.
Accepted options: --mlma --bfile adm8 --grm adm8gcta --pheno pheno_nm.txt --mpheno 50 --out adm8_nm_asstest_gcta50 --thread-num 20
Note: the program will be running on 20 threads.
Reading PLINK FAM file from [adm8.fam]. 3000 individuals to be included from [adm8.fam]. Reading PLINK BIM file from [adm8.bim]. 994596 SNPs to be included from [adm8.bim]. Warning: Duplicated SNP ID "M_994595" has been changed to "M_994595_994596" .Reading PLINK BED file from [adm8.bed] in SNP-major format ... Genotype data for 3000 individuals and 994596 SNPs to be included from [adm8.bed].
The analysis run, but only for 994596 SNPs instead of the 1727769 intended.
The BED file used does not seem to have any issue, I don't see any duplicate SNPs, and plink reports the correct number of SNPs with the same BED file:
wc -l plink.snplist 1727769 plink.snplist
Any idea what could be wrong? Many thanks in advance
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Post by jgoudet on Jul 16, 2019 23:56:09 GMT
Solved (the SNP position had been truncated)
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