Computational approaches to study the effects of small genomic variations. (Q30378925)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26350246%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

title

Computational approaches to study the effects of small genomic variations (English)

1 reference

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23 February 2020

4

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23 February 2020

author name string

Kamil Khafizov

series ordinal

1

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23 February 2020

Maxim V Ivanov

series ordinal

2

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23 February 2020

Olga V Glazova

series ordinal

3

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23 February 2020

publication date

8 September 2015

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26350246%20AND%20SRC:MED&resulttype=core&format=json

Journal of Molecular Modeling

23 February 2020

published in

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26350246%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

volume

21

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26350246%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

issue

10

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23 February 2020

page(s)

251

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Nature of the protein universe

23 February 2020

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21 January 2018

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21 January 2018

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21 January 2018

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The hydrophobic moment detects periodicity in protein hydrophobicity

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Identification and functions of usefully disordered proteins

21 January 2018

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Intrinsic disorder in cell-signaling and cancer-associated proteins

21 January 2018

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Predicting intrinsic disorder in proteins: an overview

21 January 2018

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The importance of intrinsic disorder for protein phosphorylation

21 January 2018

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CAPRI rounds 3-5 reveal promising successes and future challenges for RosettaDock

21 January 2018

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DDIG-in: detecting disease-causing genetic variations due to frameshifting indels and nonsense mutations employing sequence and structural properties at nucleotide and protein levels.

21 January 2018

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

21 January 2018

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

21 January 2018

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Ranking insertion, deletion and nonsense mutations based on their effect on genetic information

21 January 2018

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A general framework for estimating the relative pathogenicity of human genetic variants

21 January 2018

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Quantitative prediction of the effect of genetic variation using hidden Markov models

21 January 2018

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

21 January 2018

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PaPI: pseudo amino acid composition to score human protein-coding variants.

21 January 2018

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Discriminating between deleterious and neutral non-frameshifting indels based on protein interaction networks and hybrid properties.

21 January 2018

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Exome sequencing as a tool for Mendelian disease gene discovery

21 January 2018

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Evolution and functional impact of rare coding variation from deep sequencing of human exomes

21 January 2018

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Harnessing red cell membrane pathophysiology towards point-of-care diagnosis for sickle cell disease

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21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00894-015-2794-Y

Structural and functional restraints on the occurrence of single amino acid variations in human proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00894-015-2794-Y

Collective judgment predicts disease-associated single nucleotide variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00894-015-2794-Y

PredictSNP: robust and accurate consensus classifier for prediction of disease-related mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00894-015-2794-Y

PON-P: integrated predictor for pathogenicity of missense variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00894-015-2794-Y

A synonymous mutation in the CFTR gene causes aberrant splicing in an italian patient affected by a mild form of cystic fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00894-015-2794-Y

A synonymous variant in IRGM alters a binding site for miR-196 and causes deregulation of IRGM-dependent xenophagy in Crohn's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00894-015-2794-Y

Searching for polymorphisms that affect gene expression and mRNA processing: example ABCB1 (MDR1).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00894-015-2794-Y

Human catechol-O-methyltransferase haplotypes modulate protein expression by altering mRNA secondary structure.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00894-015-2794-Y

A "silent" polymorphism in the MDR1 gene changes substrate specificity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00894-015-2794-Y

Bioinformatics challenges for personalized medicine

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00894-015-2794-Y

A reality check for alignments and trees

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00894-015-2794-Y

Is there a biological cost of protein disorder? Analysis of cancer-associated mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00894-015-2794-Y

Evaluation of disorder predictions in CASP5

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00894-015-2794-Y

Performance of mutation pathogenicity prediction methods on missense variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00894-015-2794-Y

21 January 2018

1 reference

12 December 2020

Two novel PRP31 premessenger ribonucleic acid processing factor 31 homolog mutations including a complex insertion-deletion identified in Chinese families with retinitis pigmentosa

1 reference

12 December 2020

Assessment of computational methods for predicting the effects of missense mutations in human cancers

1 reference

12 December 2020

Calmodulin signaling: analysis and prediction of a disorder-dependent molecular recognition

1 reference

12 December 2020

The cancer genome atlas research network: a sight to behold

1 reference

12 December 2020

10.1007/S00894-015-2794-Y

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26350246%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

1 reference