(Q36088522)

12 August 2017

KD4v: Comprehensible Knowledge Discovery System for Missense Variant (English)

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12 August 2017

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8

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12 August 2017

11

Odile Lecompte

1 reference

12 August 2017

Tien-Dao Luu

1

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12 August 2017

Alin Rusu

2

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12 August 2017

Vincent Walter

3

1 reference

12 August 2017

Benjamin Linard

4

1 reference

12 August 2017

Laetitia Poidevin

5

1 reference

12 August 2017

Raymond Ripp

6

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12 August 2017

Luc Moulinier

7

1 reference

12 August 2017

Wolfgang Raffelsberger

9

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12 August 2017

Nicolas Wicker

10

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12 August 2017

Julie D Thompson

12

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12 August 2017

Olivier Poch

13

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12 August 2017

Hoan Nguyen

14

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12 August 2017

language of work or name

English

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publication date

27 May 2012

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12 August 2017

Nucleic Acids Research

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12 August 2017

40

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12 August 2017

Web Server issue

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12 August 2017

W71-5

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Creative Commons Attribution-NonCommercial 3.0 Unported

12 August 2017

start time

5 October 2016

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

MSV3d: database of human MisSense Variants mapped to 3D protein structure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3394327

SNPdbe: constructing an nsSNP functional impacts database

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3394327

M-ORBIS: mapping of molecular binding sites and surfaces

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3394327

A method and server for predicting damaging missense mutations

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3394327

Easy retrieval of single amino-acid polymorphisms and phenotype information using SwissVar

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3394327

SM2PH-db: an interactive system for the integrated analysis of phenotypic consequences of missense mutations in proteins involved in human genetic diseases.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3394327

Functional annotations improve the predictive score of human disease-related mutations in proteins

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3394327

SNAP predicts effect of mutations on protein function

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3394327

Protein structure modeling with MODELLER

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3394327

Data growth and its impact on the SCOP database: new developments

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3394327

MACSIMS: multiple alignment of complete sequences information management system

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3394327

SNPs3D: candidate gene and SNP selection for association studies.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3394327

nsSNPAnalyzer: identifying disease-associated nonsynonymous single nucleotide polymorphisms

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3394327

I-Mutant2.0: predicting stability changes upon mutation from the protein sequence or structure

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3394327

PANTHER: a library of protein families and subfamilies indexed by function

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3394327

PipeAlign: A new toolkit for protein family analysis

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3394327

SIFT: Predicting amino acid changes that affect protein function

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3394327

Automated analysis of interatomic contacts in proteins

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3394327

Décrypthon grid - grid resources dedicated to neuromuscular disorders.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3394327

Inductive logic programming

23 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FNAR%2FGKS474

Performance of mutation pathogenicity prediction methods on missense variants

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FNAR%2FGKS474

21 January 2018

Identifiers

DOI

10.1093/NAR/GKS474

1 reference

journals/nar/LuuRWLPRMMRWLTPN12

12 August 2017

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference

12 August 2017

1 reference