TIARA: a database for accurate analysis of multiple personal genomes based on cross-technology - Wikidata - awgldk - TriplyDB

TIARA: a database for accurate analysis of multiple personal genomes based on cross-technology

TIARA: a database for accurate analysis of multiple personal genomes based on cross-technology

http://www.wikidata.org/entity/Q24613521

about

Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing Sequencing technologies and genome sequencing Recessive C10orf2 mutations in a family with infantile-onset spinocerebellar ataxia, sensorimotor polyneuropathy, and myopathy TIARA genome database: update 2013.Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families FX: an RNA-Seq analysis tool on the cloud.Exploring the implications of INDELs in neuropsychiatric genetics: challenges and perspectives.Two Korean siblings with recently described ovarioleukodystrophy related to AARS2 mutations.Exome sequencing is an efficient tool for genetic screening of Charcot-Marie-Tooth disease.Extensive genomic and transcriptional diversity identified through massively parallel DNA and RNA sequencing of eighteen Korean individuals.

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TIARA: a database for accurate analysis of multiple personal genomes based on cross-technology

http://www.wikidata.org/entity/Q24613521

description

2011 nî lūn-bûn

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2011 թուականի Յունուարին հրատարակուած գիտական յօդուած

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2011 թվականի հունվարին հրատարակված գիտական հոդված

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2011年の論文

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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TIARA: a database for accurate ...... omes based on cross-technology

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Dongwan Hong

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Hansoo Park

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Jeong-Sun Seo

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Jong-Il Kim

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Jong-Yeon Shin

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Saet-Byeol Yu

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Seungbok Lee

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Sheehyun Kim

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Sujung Kim

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Sung-Soo Park

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P2860

The diploid genome sequence of an individual human

The diploid genome sequence of an Asian individual

Personal genome sequencing: current approaches and challenges

The complete genome of an individual by massively parallel DNA sequencing

Accurate whole human genome sequencing using reversible terminator chemistry

Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding

Paired-end mapping reveals extensive structural variation in the human genome

Global variation in copy number in the human genome

Detection of large-scale variation in the human genome

Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays

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10.1093/NAR/GKQ1101

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39

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