Log in to save to my catalogue

CAUSEL: an epigenome- and genome-editing pipeline for establishing function of noncoding GWAS varian...

CAUSEL: an epigenome- and genome-editing pipeline for establishing function of noncoding GWAS varian...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1808617411

CAUSEL: an epigenome- and genome-editing pipeline for establishing function of noncoding GWAS variants

About this item

Full title

CAUSEL: an epigenome- and genome-editing pipeline for establishing function of noncoding GWAS variants

Publisher

New York: Nature Publishing Group US

Journal title

Nature medicine, 2015-11, Vol.21 (11), p.1357-1363

Language

English

Formats

Publication information

Publisher

New York: Nature Publishing Group US

More information

Scope and Contents

Contents

A pipeline incorporating genetic fine mapping, epigenome editing, and genome editing enables functional analysis of disease-associated SNPs located in non-protein-coding regions of the genome.
The vast majority of disease-associated single-nucleotide polymorphisms (SNPs) mapped by genome-wide association studies (GWASs) are located in the non-pr...

Alternative Titles

Full title

CAUSEL: an epigenome- and genome-editing pipeline for establishing function of noncoding GWAS variants

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_1808617411

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1808617411

Other Identifiers

ISSN

1078-8956

E-ISSN

1546-170X

DOI

10.1038/nm.3975

How to access this item