Hi,
I want to import a vcf file which I created using GATK via 34 gvcf files merged using gvcf genotyper. I want to import the file into Plink to create a .raw and .map which I can import to R for use with the adegenet package.
My plink1.9 command line is:
./plink --vcf SNPs_34_combined_filtered.vcf --allow-extra-chr --double-id --biallelic-only --vcf-filter GATK_HQ_fail --recode A --out SNPs_34_combined_filtered
The error I get is
--vcf: 432k variants complete.Error: Too many distinct nonstandard chromosome/contig names.
The reference I used for SNP calling in GATK was a denovo assembled fasta with 9979 scaffolds
Thanks for any help