Reference-unbiased copy number variant analysis using CGH microarrays - Wikidata - awgldk - TriplyDB

Reference-unbiased copy number variant analysis using CGH microarrays

Reference-unbiased copy number variant analysis using CGH microarrays

http://www.wikidata.org/entity/Q34298242

about

TIARA: a database for accurate analysis of multiple personal genomes based on cross-technology Increased de novo copy number variants in the offspring of older males Global assessment of genomic variation in cattle by genome resequencing and high-throughput genotyping.Genetic association studies of copy-number variation: should assignment of copy number states precede testing?The first Irish genome and ways of improving sequence accuracy TIARA genome database: update 2013.CNV instability associated with DNA replication dynamics: evidence for replicative mechanisms in CNV mutagenesis.Family-Based Benchmarking of Copy Number Variation Detection Software.Identification of functionally active, low frequency copy number variants at 15q21.3 and 12q21.31 associated with prostate cancer risk.Increased genome instability in human DNA segments with self-chains: homology-induced structural variations via replicative mechanisms tRNA gene copy number variation in humans.Copy Number Variations in Candidate Genes and Intergenic Regions Affect Body Mass Index and Abdominal Obesity in Mexican Children Copy number variation in transcriptionally active regions of sexual and apomictic Boechera demonstrates independently derived apomictic lineages.Complex brain malformations associated with chromosome 6q27 gain that includes THBS2, which encodes thrombospondin 2, an astrocyte-derived protein of the extracellular matrix.Extensive genomic and transcriptional diversity identified through massively parallel DNA and RNA sequencing of eighteen Korean individuals.

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Reference-unbiased copy number variant analysis using CGH microarrays

http://www.wikidata.org/entity/Q34298242

description

2010 nî lūn-bûn

@nan

2010 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2010年の論文

@ja

2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

Reference-unbiased copy number variant analysis using CGH microarrays

@ast

Reference-unbiased copy number variant analysis using CGH microarrays

@en

Reference-unbiased copy number variant analysis using CGH microarrays

@nl

type

label

Reference-unbiased copy number variant analysis using CGH microarrays

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Reference-unbiased copy number variant analysis using CGH microarrays

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Reference-unbiased copy number variant analysis using CGH microarrays

@nl

prefLabel

Reference-unbiased copy number variant analysis using CGH microarrays

@ast

Reference-unbiased copy number variant analysis using CGH microarrays

@en

Reference-unbiased copy number variant analysis using CGH microarrays

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Nucleic Acids Research

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Reference-unbiased copy number variant analysis using CGH microarrays

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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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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

Initial sequencing and analysis of the human genome

The diploid genome sequence of an Asian individual

Fine-scale structural variation of the human genome

Mapping and sequencing of structural variation from eight human genomes

The complete genome of an individual by massively parallel DNA sequencing

Accurate whole human genome sequencing using reversible terminator chemistry

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

Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation

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