A comprehensive study of small non-frameshift insertions/deletions in proteins and prediction of their phenotypic effects by a machine learning method (KD4i). (Q33612884)

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English	A comprehensive study of small non-frameshift insertions/deletions in proteins and prediction of their phenotypic effects by a machine learning method (KD4i).	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

28 July 2017

A comprehensive study of small non-frameshift insertions/deletions in proteins and prediction of their phenotypic effects by a machine learning method (KD4i). (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

machine learning

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author name string

Carlos Bermejo-Das-Neves

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Hoan-Ngoc Nguyen

2

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Olivier Poch

3

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Julie D Thompson

4

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Europe PubMed Central

PubMed publication ID

28 July 2017

publication date

17 April 2014

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Europe PubMed Central

PubMed publication ID

28 July 2017

BMC Bioinformatics

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Europe PubMed Central

PubMed publication ID

28 July 2017

15

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Europe PubMed Central

PubMed publication ID

28 July 2017

111

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

SIFT Indel: predictions for the functional effects of amino acid insertions/deletions in proteins

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DDIG-in: discriminating between disease-associated and neutral non-frameshifting micro-indels

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Spastic paraplegia mutation N256S in the neuronal microtubule motor KIF5A disrupts axonal transport in a Drosophila HSP model

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New and continuing developments at PROSITE.

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14 July 2018

Predicting the functional effect of amino acid substitutions and indels

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Evolutionary diagnosis method for variants in personal exomes

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KD4v: Comprehensible Knowledge Discovery System for Missense Variant

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14 July 2018

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14 July 2018

Natural genetic variation caused by small insertions and deletions in the human genome

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14 July 2018

Small insertions and deletions (INDELs) in human genomes

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14 July 2018

A method and server for predicting damaging missense mutations

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14 July 2018

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

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14 July 2018

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

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14 July 2018

The UCSC Genome Browser database: update 2010

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14 July 2018

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

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14 July 2018

Next-generation DNA sequencing

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14 July 2018

Genetic variation in an individual human exome

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14 July 2018

The complete genome of an individual by massively parallel DNA sequencing

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14 July 2018

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14 July 2018

Database resources of the National Center for Biotechnology Information

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14 July 2018

An initial map of insertion and deletion (INDEL) variation in the human genome.

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14 July 2018

Predicting the effects of amino acid substitutions on protein function

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14 July 2018

A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10)

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14 July 2018

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14 July 2018

Origins of structure in globular proteins

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Parathyroid MEN1 gene mutations in relation to clinical characteristics of nonfamilial primary hyperparathyroidism

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Sequence-based prediction of pathological mutations

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based on heuristic

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1000 Genomes project

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Identifiers

10.1186/1471-2105-15-111

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

DBLP publication ID

journals/bmcbi/Bermejo-Das-NevesNPT14

1 reference

DBLP Dataset 2021-01-02

28 January 2021

Dimensions Publication ID

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PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

ResearchGate publication ID

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