(Q34176004)

31 July 2017

title

Incorporating predicted functions of nonsynonymous variants into gene-based analysis of exome sequencing data: a comparative study (English)

1 reference

31 July 2017

Peng Wei

1

0 references

author name string

Xiaoming Liu

series ordinal

2

1 reference

31 July 2017

Yun-Xin Fu

series ordinal

3

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31 July 2017

publication date

29 November 2011

1 reference

31 July 2017

1 reference

31 July 2017

volume

5 Suppl 9

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31 July 2017

page(s)

S20

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Creative Commons Attribution 2.0 Generic

31 July 2017

copyright license

start time

29 November 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Genetic Analysis Workshop 17 mini-exome simulation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287855

Network-based genomic discovery: application and comparison of Markov random field models

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287855

MutationTaster evaluates disease-causing potential of sequence alterations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287855

Uncovering the roles of rare variants in common disease through whole-genome sequencing

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287855

Pooled association tests for rare variants in exon-resequencing studies

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287855

A method and server for predicting damaging missense mutations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287855

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287855

A groupwise association test for rare mutations using a weighted sum statistic

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287855

SNAP predicts effect of mutations on protein function

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287855

Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287855

Using SIFT and PolyPhen to predict loss-of-function and gain-of-function mutations

5 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1753-6561-5-S9-S20

A simple implementation of a normal mixture approach to differential gene expression in multiclass microarrays

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1753-6561-5-S9-S20

10.1186/1753-6561-5-S9-S20

21 January 2018

Identifiers

DOI

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Fatcat

https://api.fatcat.wiki/v0/release/fpn6aunvofelrp7v32chuojx2e

30 July 2022

Dimensions Publication ID

1004468246

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Fatcat ID

release_fpn6aunvofelrp7v32chuojx2e

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Fatcat

https://api.fatcat.wiki/v0/release/fpn6aunvofelrp7v32chuojx2e

30 July 2022

https://api.fatcat.wiki/v0/release/fpn6aunvofelrp7v32chuojx2e

1 reference

30 July 2022

https://api.fatcat.wiki/v0/release/fpn6aunvofelrp7v32chuojx2e

1 reference

30 July 2022