The fine-mapped associations of 35 lab biomarkers described in 'Genetics of 35 blood and urine biomarkers in the UK Biobank'
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https://nih.figshare.com/articles/The_fine-mapped_associations_of_35_lab_biomarkers_described_in_Genetics_of_35_blood_and_urine_biomarkers_in_the_UK_Biobank_/12344351
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The dataset contains the output from FINEMAP, a software to identify causal variants from genome-wide association summary statistics, for 35 biomarker traits described in the following preprint:<br>N. Sinnott-Armstrong*, Y. Tanigawa*, et al, Genetics of 38 blood and urine biomarkers in the UK Biobank. bioRxiv, 660506 (2019). doi:10.1101/660506<br><br>Note that we are preparing a revised version of the manuscript and this dataset contains 35 (instead of 38) biomarker phenotypes.<br><br>For each trait, we provide a tar archive file which contains the full output from FINEMAP for the regions with at least one genome-wide significant associations (p < 5e-9) from the multi-ethnic GWAS meta-analysis within UK Biobank. The content of the tar archive is organized by directories, named as <code>chr[CHROM]/[TRAIT]/range[RANGE]</code>, and contains the following files: <code>GLOBAL_[TRAIT]_chr[CHROM]_range[RANGE].bdose.zst</code><code>GLOBAL_[TRAIT]_chr[CHROM]_range[RANGE].config.zst</code><code>GLOBAL_[TRAIT]_chr[CHROM]_range[RANGE].cred.zst</code><code>GLOBAL_[TRAIT]_chr[CHROM]_range[RANGE].ld.zst</code><code>GLOBAL_[TRAIT]_chr[CHROM]_range[RANGE].master.zst</code><code>GLOBAL_[TRAIT]_chr[CHROM]_range[RANGE].snp.zst</code><code>GLOBAL_[TRAIT]_chr[CHROM]_range[RANGE].z.zst</code> where, [TRAIT]<code></code><code></code>: trait name[CHROM]<code></code><code></code>: chromosome[RANGE]<code></code><code></code>: the range of the region in the format of <code>[start position]-[end position]</code>. We provide the list of traits and regions included in this data release in <code>FINEMAP.index.tsv</code>. This is a flat table with 3 columns: trait: the biomarker traitchr: chromosomerange: the range Note that we used GRCh37/hg19 genome reference in the analysis and the BETA is always reported for the alternate allele. Please check the FINEMAP paper and software documentation for the detailed explanation of the file formats. Benner, C. et al. FINEMAP: efficient variable selection using summary data from genome-wide association studies. Bioinformatics 32, 1493–1501 (2016).Christian Benner. FINEMAP. http://christianbenner.com/. Also, all the files in the tar archive is compressed with Zstandard (as indicated by the <code>.zst</code> extension). You can check the contents with <code>zstdcat</code> command and uncompress the files with <code>zstd -d [file.zst]</code>. The Zstandard software can be built from source, or simply available from conda (https://anaconda.org/conda-forge/zstd), pip (https://pypi.org/project/zstd/) or brew (https://formulae.brew.sh/formula/zstd). Please check Zstandard website (http://facebook.github.io/zstd/) for more information.
提供机构:
National Institutes of Health
创建时间:
2020-05-23



