Entering edit mode
3.8 years ago
gubrins
▴
350
Heys everybody,
I'm trying to run some ROHs with Plink from a vcf file produced by GATK, with HaplotypeCaller
and GenotypeGVCFs
. I set -ERC
from Haplotypecaller
as BP_RESOLUTION
and with GenotypeGVCFs
I included --included-non-variant-sites true
.
When I run homozyg from Plink, I get 0 ROHs:
Options in effect:
--allow-extra-chr
--bfile out_name
--homozyg
Hostname: trueno128.hpc.csic.es
Working directory: /home/ibe/gmochales/leopards/definitive/gvcf/ROHS
Start time: Tue Mar 2 11:45:39 2021
Random number seed: 1614681939
32168 MB RAM detected; reserving 16084 MB for main workspace.
9911762 variants loaded from .bim file.
1 person (0 males, 0 females, 1 ambiguous) loaded from .fam.
Ambiguous sex ID written to plink.nosex .
Using 1 thread (no multithreaded calculations invoked).
Before main variant filters, 1 founder and 0 nonfounders present.
Calculating allele frequencies... done.
Total genotyping rate is 0.912456.
9911762 variants and 1 person pass filters and QC.
Note: No phenotypes present.
--homozyg: Scan complete, found 0 ROH.
Results saved to plink.hom + plink.hom.indiv + plink.hom.summary .
Is --included-non-variant-sites
not working with the current version?
Thanks in advance!