Data description

File naming pattern and file structure

Summary association statistics

GWAS summary statistics (tab-delimited, bgzipped, genome build 38, tabixarrow-up-right index files included) are named as {endpoint}.gz. For example, endpoint I9_CHD has I9_CHD.gz and I9_CHD.gz.tbi.

To learn more about the methods used, see section GWAS.

The {endpoint}.gz have the following structure:

Column name

Description

#chrom

chromosome on build GRCh38 (1-22, X)

pos

position in base pairs on build GRCh38

ref

reference allele

alt

alternative allele (effect allele)

rsids

variant identifier

nearest_genes

nearest gene name from variant

pval

p-value from SAIGEarrow-up-right

beta

effect size estimated with SAIGEarrow-up-right for the alternative allele

sebeta

standard deviation of effect size estimated with SAIGEarrow-up-right

maf

alternative (effect) allele frequency

maf_cases

alternative (effect) allele frequency among cases

maf_controls

alternative (effect) allele frequency among controls

Fine-mapping results

Two fine-mapping methods were used:

Fine-mapping results are tab-delimited and bgzipped.

SuSiE results have the following filename pattern:

  • {endpoint}.SUSIE.cred.bgz

  • {endpoint}.SUSIE.snp.bgz

FINEMAP results have the following filename pattern:

  • {endpoint}.FINEMAP.region.bgz

  • {endpoint}.FINEMAP.snp.bgz

  • {endpoint}.FINEMAP.cred.bgz

To learn more about the methods used, see section fine-mapping.

SuSiE output files {endpoint}.SUSIE.snp.bgz have the following structure:

Column name

Description

trait

endpoint name

region

chr:start-end

v

variant identifier

rsid

rs variant identifier

chromosome

chromosome on build GRCh38 (1-22, X)

position

position in base pairs on build GRCh38

allele1

reference allele

allele2

alternative allele (effect allele)

maf

minor allele frequency

beta

effect size GWAS

se

standard error GWAS

p

p-value GWAS

mean

posterior expectation of true effect size

sd

posterior standard deviation of true effect size

prob

posterior probability of association

cs

identifier of 95% credible set (-1 = variant is not part of credible set)

LD estimation

Linkage disequilibrium (LD) was estimated from SISU v3 for each chromosome. Use the tool LDstore (v1.1)arrow-up-right for further usage of the bcor files.

ldstore --bcor FG_LD_chr1.bcor --incl-range 20000000-50000000 --table output_file_name.table

To learn more about the methods used, see section LD estimation.

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