Genome-wide analysis of human disease alleles reveals that their locations are correlated in paralogous proteins. - Test2 - elhamkhani - TriplyDB

Genome-wide analysis of human disease alleles reveals that their locations are correlated in paralogous proteins.

Genome-wide analysis of human disease alleles reveals that their locations are correlated in paralogous proteins.

http://www.wikidata.org/entity/Q33383215

about

Integrating phenotype ontologies across multiple species Single nucleotide differences (SNDs) in the dbSNP database may lead to errors in genotyping and haplotyping studies Human aldo-keto reductases and the metabolic activation of polycyclic aromatic hydrocarbons HDAM: a resource of human disease associated mutations from next generation sequencing studies Global analysis of disease-related DNA sequence variation in 10 healthy individuals: implications for whole genome-based clinical diagnostics A probabilistic disease-gene finder for personal genomes.Phevor combines multiple biomedical ontologies for accurate identification of disease-causing alleles in single individuals and small nuclear families.Functional assays provide a robust tool for the clinical annotation of genetic variants of uncertain significance.

P2860

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P2860

Genome-wide analysis of human disease alleles reveals that their locations are correlated in paralogous proteins.

http://www.wikidata.org/entity/Q33383215

description

2008 nî lūn-bûn

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2008 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2008 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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name

Genome-wide analysis of human ...... elated in paralogous proteins.

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Genome-wide analysis of human ...... elated in paralogous proteins.

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type

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Genome-wide analysis of human ...... elated in paralogous proteins.

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Genome-wide analysis of human ...... elated in paralogous proteins.

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Genome-wide analysis of human ...... elated in paralogous proteins.

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Genome-wide analysis of human ...... elated in paralogous proteins.

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JOURNAL.PCBI.1000218

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PLOS Computational Biology

P1476

Genome-wide analysis of human ...... elated in paralogous proteins.

@en

P2093

Andrew MacBride

http://www.w3.org/2001/XMLSchema#string

Barry Moore

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Charles White

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Chris Mungall

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Fidel Salas

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Mark Yandell

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Martin G Reese

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P2860

Large-scale trends in the evolution of gene structures within 11 animal genomes.

Predicting deleterious amino acid substitutions

Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1

Spectrum and frequency of jagged1 (JAG1) mutations in Alagille syndrome patients and their families

Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders

Amino acid substitution matrices from protein blocks

dbSNP: the NCBI database of genetic variation

Basic local alignment search tool

Predicting the effects of amino acid substitutions on protein function

SIFT: Predicting amino acid changes that affect protein function

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e1000218

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scholarly article

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11

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4

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18989397

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2565504

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