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If using hg38:

Source vcf files of 1000G phase 3, hg38 downloaded from: http://ftp.1000genomes.ebi.ac.uk/vol1/ftp/release/20130502/supporting/GRCh38_positions/

1000g hg38 phase 3 plink & vcf files are on oak:

/oak/stanford/groups/akundaje/refs/1000genomes

SNPs from "1000G.phase3.hg38.merged-merge.missnp" were multi-allelic, so removed from the 1000G Phase 3 VCF file set before creating the PLINK bed files.

  • The code to generate the plink files from the souce VCF files is in makebed/make_bed_1kg.sh
  • The code to filter the resulting bed/bim/fam files to Caucasian genotypes is in getcaucasian/get_samples_to_keep.sh
  • The code to calculate r^2 LD values for a GWAS summary stats file is in get_ld.sh

If using hg19:

bed/bim/fam files are on oak in /oak/stanford/groups/akundaje/refs/1000genomes/hg19
ethnicity filtering can be done with same approach as hg38 (see getcaucasian/get_samples_to_keep.sh)

Alternatively to the workflow described for hg38,Peyton Greenside has pre-computed LD for hg19, with those files here:

/mnt/lab_data/kundaje/users/pgreens/LD

these are cited on zenodo: https://zenodo.org/record/3404275#.X9GGBpNKgxM

So you can grep for the rsid's of interest in these files.

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