Developments in FINDbase worldwide database for clinically relevant genomic variation allele frequencies - Wikidata - wikimedia - TriplyDB

Developments in FINDbase worldwide database for clinically relevant genomic variation allele frequencies

Developments in FINDbase worldwide database for clinically relevant genomic variation allele frequencies

http://www.wikidata.org/entity/Q24567762

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ePGA: A Web-Based Information System for Translational Pharmacogenomics A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics Genomics into Healthcare: the 5th Pan Arab Human Genetics Conference and 2013 Golden Helix Symposium A pan-cancer analysis of prognostic genes.GenInfoGuard--a robust and distortion-free watermarking technique for genetic data.Calling genotypes from public RNA-sequencing data enables identification of genetic variants that affect gene-expression levels Expanded national database collection and data coverage in the FINDbase worldwide database for clinically relevant genomic variation allele frequencies.Variation Interpretation Predictors: Principles, Types, Performance, and Choice.HEROD: a human ethnic and regional specific omics database.Human genotype-phenotype databases: aims, challenges and opportunities.β-Thalassemia Haplotypes in Romania in the Context of Genetic Mixing in the Mediterranean Area.β-Thalassemia gene mutations in Antalya, Turkey: results from a single centre study.Pharmacogenomics education and research at the Department of Pharmacy, University of Patras, Greece.The 24th annual Nucleic Acids Research database issue: a look back and upcoming changes.Bridging genomics research between developed and developing countries: the Genomic Medicine Alliance

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P2860

Developments in FINDbase worldwide database for clinically relevant genomic variation allele frequencies

http://www.wikidata.org/entity/Q24567762

description

2014 nî lūn-bûn

@nan

2014 թուականի Յունուարին հրատարակուած գիտական յօդուած

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2014 թվականի հունվարին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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name

Developments in FINDbase world ...... c variation allele frequencies

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Developments in FINDbase world ...... c variation allele frequencies

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Developments in FINDbase world ...... c variation allele frequencies

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Developments in FINDbase world ...... c variation allele frequencies

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Developments in FINDbase world ...... c variation allele frequencies

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Developments in FINDbase world ...... c variation allele frequencies

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Developments in FINDbase world ...... c variation allele frequencies

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Developments in FINDbase world ...... c variation allele frequencies

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Developments in FINDbase world ...... c variation allele frequencies

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Nucleic Acids Research

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Developments in FINDbase world ...... c variation allele frequencies

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Abdelaziz Sefiani

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Cristiana Pavlidis

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Emmanouil Viennas

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George P Patrinos

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Ilham Ratbi

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John Tsaknakis

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Konstantinos Poulas

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Marina Bartsakoulia

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Vassiliki Gkantouna

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Zafeiria-Marina Ioannou

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P2860

Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach

FINDbase: a worldwide database for genetic variation allele frequencies updated

Cystic fibrosis: a worldwide analysis of CFTR mutations--correlation with incidence data and application to screening

Microattribution and nanopublication as means to incentivize the placement of human genome variation data into the public domain

Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collection.

Population-ethnic group specific genome variation allele frequency data: a querying and visualization journey.

Documentation of inherited disorders and mutation frequencies in the different religious communities in Israel in the Israeli National Genetic Database.

Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies

Pharmacogenetics: a practical role in predicting antiretroviral drug toxicity?

FINDbase: a relational database recording frequencies of genetic defects leading to inherited disorders worldwide.

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scholarly article

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3493532

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10.1093/NAR/GKT1125

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Database issue

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42

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Petros Papadopoulos

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2014-01-01T00:00:00Z

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