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I am running PCA for 1kGP merged SV vcf files and I am getting the seg fault error when I run the PBS script with 150G memory. The run command is in the last line. It worked fine when I extracted a single chromosome (chr21) from the VCF and run the same script.
Input: bcftool_merge.sv_chr1_22_maf_ge0.05.annotated.vcf.gz
MAF lower bound: 0
Thin: 1
Number principle components: 20
Reading data...
1793 samples
Kept 2028657 markers out of 2028657
/var/spool/torque/mom_priv/jobs/3377732.sug-moab.SC: line 12: 11059 Segmentation fault /hgsc_software/akt/akt-0.3.3/bin/akt pca ${vcf}.vcf.gz --force -Oz -o ${vcf}.pca.cf.gz > ${vcf}.txt
The text was updated successfully, but these errors were encountered:
I got it. Yes, it's merged SVs of all 3,202 so it contains too many variants. I actually extracted the variants with MAF > 0.05 (using bcftools). I think the MAF input parameter option in AKT is not working although I see some lines in the source code.
I am running PCA for 1kGP merged SV vcf files and I am getting the seg fault error when I run the PBS script with 150G memory. The run command is in the last line. It worked fine when I extracted a single chromosome (chr21) from the VCF and run the same script.
The text was updated successfully, but these errors were encountered: