Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing.
about
COPS: a sensitive and accurate tool for detecting somatic Copy Number Alterations using short-read sequence data from paired samplesA preliminary study of copy number variation in TibetansGenome-wide copy number analysis uncovers a new HSCR gene: NRG3Towards a comprehensive structural variation map of an individual human genomeHuman genetics and genomics a decade after the release of the draft sequence of the human genomeThe genetics of attention deficit/hyperactivity disorder in adults, a reviewSHANK1 Deletions in Males with Autism Spectrum DisorderAccurate and comprehensive sequencing of personal genomesTIARA: a database for accurate analysis of multiple personal genomes based on cross-technologyGenome-wide association analyses identify 18 new loci associated with serum urate concentrationsIntegrating genetics and epigenetics in breast cancer: biological insights, experimental, computational methods and therapeutic potentialSInC: an accurate and fast error-model based simulator for SNPs, Indels and CNVs coupled with a read generator for short-read sequence dataClinical implementation of whole-genome array CGH as a first-tier test in 5080 pre and postnatal casesExploring the role of copy number variants in human adaptationGenome-wide association analysis identifies 13 new risk loci for schizophreniaCNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencingRoutes for breaching and protecting genetic privacyCopy number variation of age-related macular degeneration relevant genes in the Korean populationComparative analysis of copy number variation detection methods and database constructionGenome-wide association analyses of esophageal squamous cell carcinoma in Chinese identify multiple susceptibility loci and gene-environment interactionsGenome-wide association study identifies a new melanoma susceptibility locus at 1q21.3Network biology concepts in complex disease comorbiditiesSeven prostate cancer susceptibility loci identified by a multi-stage genome-wide association studyGenome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder.The genome-wide landscape of copy number variations in the MUSGEN study provides evidence for a founder effect in the isolated Finnish population.Simultaneous copy number losses within multiple subtelomeric regions in early-onset type 2 diabetes mellitusTUFT1, a novel candidate gene for metatarsophalangeal osteoarthritis, plays a role in chondrogenesis on a calcium-related pathwayIncreased CNV-region deletions in mild cognitive impairment (MCI) and Alzheimer's disease (AD) subjects in the ADNI sampleEvaluation of copy number variation detection for a SNP array platform.Positive selection of primate genes that promote HIV-1 replication.Ultra high throughput sequencing in human DNA variation detection: a comparative study on the NDUFA3-PRPF31 region.An initial comparative map of copy number variations in the goat (Capra hircus) genomeA genomic copy number variant analysis implicates the MBD5 and HNRNPU genes in Chinese children with infantile spasms and expands the clinical spectrum of 2q23.1 deletionUse of clinical chromosomal microarray in Chinese patients with autism spectrum disorder-implications of a copy number variation involving DPP10Data-driven approach to detect common copy-number variations and frequency profiles in a population-based Korean cohort.Relating CNVs to transcriptome data at fine resolution: assessment of the effect of variant size, type, and overlap with functional regions.Genome-wide detection of copy number variations among diverse horse breeds by array CGH.A multi-sample based method for identifying common CNVs in normal human genomic structure using high-resolution aCGH dataGlobal assessment of genomic variation in cattle by genome resequencing and high-throughput genotyping.A map of copy number variations in Chinese populations.
P2860
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P2860
Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing.
description
2010 nî lūn-bûn
@nan
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
2010年论文
@zh
2010年论文
@zh-cn
name
Discovery of common Asian copy ...... ively parallel DNA sequencing.
@ast
Discovery of common Asian copy ...... ively parallel DNA sequencing.
@en
type
label
Discovery of common Asian copy ...... ively parallel DNA sequencing.
@ast
Discovery of common Asian copy ...... ively parallel DNA sequencing.
@en
prefLabel
Discovery of common Asian copy ...... ively parallel DNA sequencing.
@ast
Discovery of common Asian copy ...... ively parallel DNA sequencing.
@en
P2093
P2860
P50
P356
P1433
P1476
Discovery of common Asian copy ...... ively parallel DNA sequencing.
@en
P2093
Charles Lee
Dongwhan Suh
Ga-Ram Hwang
Hansoo Park
Hyeran Kim
Hyun-Jin Kim
Hyungtae Kim
Hyunseok Peter Kang
Jeong-Sun Seo
Jong-Il Kim
P2860
P2888
P304
P356
10.1038/NG.555
P407
P577
2010-04-04T00:00:00Z
P5875
P6179
1006886726