(Q46952242)

26 December 2017

title

Use of estimated evolutionary strength at the codon level improves the prediction of disease-related protein mutations in humans (English)

1 reference

26 December 2017

author

Emidio Capriotti

1

1 reference

26 December 2017

Marc A. Martí‐Renom

6

1 reference

26 December 2017

Joaquín Dopazo

object named as

Joaquín Dopazo

4

0 references

Rita Casadio

3

object named as

Rita Casadio

1 reference

26 December 2017

Leonardo Arbiza

2

1 reference

26 December 2017

Hernán Dopazo

5

1 reference

26 December 2017

publication date

1 January 2008

1 reference

26 December 2017

published in

Human Mutation

1 reference

26 December 2017

volume

29

1 reference

26 December 2017

issue

1

1 reference

26 December 2017

page(s)

198-204

1 reference

26 December 2017

Basic local alignment search tool

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

Understanding mutations and protein stability through tripeptides.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

Selective Pressures at a Codon-level Predict Deleterious Mutations in Human Disease Genes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

The Universal Protein Resource (UniProt)

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

Assessing the accuracy of prediction algorithms for classification: an overview

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

Prediction of the phenotypic effects of non-synonymous single nucleotide polymorphisms using structural and evolutionary information.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

nsSNPAnalyzer: identifying disease-associated nonsynonymous single nucleotide polymorphisms

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

Predicting protein stability changes from sequences using support vector machines

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

Predicting the insurgence of human genetic diseases associated to single point protein mutations with support vector machines and evolutionary information

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

Deleterious SNP prediction: be mindful of your training data!

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

Characterization of single-nucleotide polymorphisms in coding regions of human genes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

Interpreting missense variants: comparing computational methods in human disease genes CDKN2A, MLH1, MSH2, MECP2, and tyrosinase (TYR).

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

Training v-Support Vector Classifiers: Theory and Algorithms

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

A DNA Polymorphism Discovery Resource for Research on Human Genetic Variation: Table 1

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

MUSCLE: a multiple sequence alignment method with reduced time and space complexity

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

Molecular basis of mucopolysaccharidosis type II: mutations in the iduronate-2-sulphatase gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

https://api.crossref.org/works/10.1002%2FHUMU.20628

1 reference

7 January 2021

LS-SNP: large-scale annotation of coding non-synonymous SNPs based on multiple information sources.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

Human Gene Mutation Database?A biomedical information and research resource

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

Cd-hit: a fast program for clustering and comparing large sets of protein or nucleotide sequences

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

Accounting for human polymorphisms predicted to affect protein function

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

SIFT: Predicting amino acid changes that affect protein function

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

Human non-synonymous SNPs: server and survey

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

A phylogenetic approach to assessing the significance of missense mutations in disease genes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

dbSNP: the NCBI database of genetic variation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

Molecules consolidate the placental mammal tree

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

Human Gene Mutation Database (HGMD): 2003 update

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

Assessing the relative importance of the biophysical properties of amino acid substitutions associated with human genetic disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

PANTHER: a browsable database of gene products organized by biological function, using curated protein family and subfamily classification

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

Bayes empirical bayes inference of amino acid sites under positive selection

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

Identification and analysis of deleterious human SNPs.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20628

7 January 2021

Identifiers

DOI

10.1002/HUMU.20628

1 reference

26 December 2017

1 reference

26 December 2017