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FORGEdb: a tool for identifying candidate functional variants and uncovering target genes and mechanisms for complex diseases

descriptionPublicationkeyboard_double_arrow_right Article 28 Aug 2023Publisher:Zenodo
Authors: Breeze, Charles;

doi: 10.5281/zenodo.10067458 , 10.5281/zenodo.10067457 , 10.5281/zenodo.8293407 , 10.5281/zenodo.8293408

FORGEdb: a tool for identifying candidate functional variants and uncovering target genes and mechanisms for complex diseases

Abstract

This dataset contains files associated with the manuscript "FORGEdb: a tool for identifying candidate functional variants and uncovering target genes and mechanisms for complex diseases". This manuscript presents Functional element Overlap analysis of the Results of GWAS Experiments database (FORGEdb), a new method for analysing genetic variants and their regulatory context. FORGEdb scores for 37 million variants (as of 28 August 2023) are contained in the compressed file rsid.scores.final.s.txt.zip FORGEdb code is contained on GitHub at https://github.com/CBIIT/nci-webtools-dceg-forgedb/tree/forgedb_1.0.0

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popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
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influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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