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Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for twelve imm...

Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for twelve imm...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2338875807

Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for twelve immune-mediated diseases

About this item

Full title

Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for twelve immune-mediated diseases

Publisher

Cold Spring Harbor: Cold Spring Harbor Laboratory Press

Journal title

bioRxiv, 2020-01

Language

English

Formats

Publication information

Publisher

Cold Spring Harbor: Cold Spring Harbor Laboratory Press

More information

Scope and Contents

Contents

The identification of causal genetic variants for common diseases improves understanding of disease biology. Here we use data from the BLUEPRINT project to identify regulatory quantitative trait loci (QTL) for three primary human immune cell types and use these to fine-map putative causal variants for twelve immune-mediated diseases. We identify 34...

Alternative Titles

Full title

Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for twelve immune-mediated diseases

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_journals_2338875807

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2338875807

Other Identifiers

ISSN

2692-8205

E-ISSN

2692-8205

DOI

10.1101/2020.01.15.907436

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