(Q50558398)

15 March 2018

title

Diving deeper to predict noncoding sequence function. (English)

1 reference

15 March 2018

author

Barbara E. Engelhardt

series ordinal

1

1 reference

15 March 2018

author name string

Christopher D Brown

series ordinal

2

1 reference

15 March 2018

publication date

1 September 2015

1 reference

15 March 2018

published in

Nature Methods

1 reference

15 March 2018

volume

12

1 reference

15 March 2018

issue

10

1 reference

15 March 2018

page(s)

925-926

1 reference

15 March 2018

https://scigraph.springernature.com/pub.10.1038/nmeth.3604

exact match

0 references

cites work

Predicting effects of noncoding variants with deep learning-based sequence model

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3604

Joint analysis of functional genomic data and genome-wide association studies of 18 human traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3604

Distribution and intensity of constraint in mammalian genomic sequence

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3604

Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3604

Recessive mutations in a distal PTF1A enhancer cause isolated pancreatic agenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3604

An integrated encyclopedia of DNA elements in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3604

An atlas of active enhancers across human cell types and tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3604

Integrative analysis of 111 reference human epigenomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3604

A general framework for estimating the relative pathogenicity of human genetic variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3604

A method for calculating probabilities of fitness consequences for point mutations across the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3604

Functional annotation of noncoding sequence variants.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3604

A method to predict the impact of regulatory variants from DNA sequence

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3604

Massively parallel functional dissection of mammalian enhancers in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.3604

21 January 2018

Identifiers

DOI

10.1038/NMETH.3604

1 reference

15 March 2018

1 reference

15 March 2018