(Q34555349)

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

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scholarly article

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Europe PubMed Central

PubMed publication ID

3 August 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

vector-borne disease

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support vector machine

1 reference

based on heuristic

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author name string

Capriotti E

1

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Calabrese R

2

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Casadio R

3

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Europe PubMed Central

PubMed publication ID

3 August 2017

language of work or name

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publication date

7 August 2006

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Europe PubMed Central

PubMed publication ID

3 August 2017

number of pages

6

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based on heuristic

inferred from page(s)

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Europe PubMed Central

PubMed publication ID

3 August 2017

22

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Europe PubMed Central

PubMed publication ID

3 August 2017

22

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

2729-2734

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

describes a project that uses

support vector machine

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based on heuristic

inferred from title

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

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTL423

21 January 2018

Assessing the accuracy of prediction algorithms for classification: an overview

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTL423

21 January 2018

Africans and Asians abroad: genetic diversity in Europe

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTL423

21 January 2018

Predicting disease using genomics

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTL423

21 January 2018

The SWISS-PROT protein knowledgebase and its supplement TrEMBL in 2003

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTL423

21 January 2018

Predicting protein stability changes from sequences using support vector machines

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTL423

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTL423

21 January 2018

Carbohydrate Structure Suite (CSS): analysis of carbohydrate 3D structures derived from the PDB

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTL423

21 January 2018

Mutations arising in the wave front of an expanding population

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTL423

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTL423

21 January 2018

Clustering of highly homologous sequences to reduce the size of large protein databases

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTL423

21 January 2018

Accounting for human polymorphisms predicted to affect protein function

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTL423

21 January 2018

SIFT: Predicting amino acid changes that affect protein function

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTL423

21 January 2018

Human non-synonymous SNPs: server and survey

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTL423

21 January 2018

SNPeffect: a database mapping molecular phenotypic effects of human non-synonymous coding SNPs

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTL423

21 January 2018

SNPper: retrieval and analysis of human SNPs

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTL423

21 January 2018

dbSNP: the NCBI database of genetic variation

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTL423

21 January 2018

Human Gene Mutation Database (HGMD): 2003 update

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTL423

21 January 2018

Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTL423

21 January 2018

SNPs, protein structure, and disease.

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTL423

21 January 2018

Identification and analysis of deleterious human SNPs.

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTL423

21 January 2018

Understanding human diversity

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTL423

21 January 2018

Identifiers

10.1093/BIOINFORMATICS/BTL423

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

DBLP publication ID

journals/bioinformatics/CapriottiCC06

1 reference

DBLP Dataset 2021-01-02

28 January 2021

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

ResearchGate publication ID

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