Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants
about
A preliminary study of copy number variation in TibetansDetectable clonal mosaicism and its relationship to aging and cancerRare deletions at the neurexin 3 locus in autism spectrum disorderSHANK1 Deletions in Males with Autism Spectrum DisorderUsing ERDS to infer copy-number variants in high-coverage genomesMicroarray resources for genetic and genomic studies in chicken: a reviewComputational methods for detecting copy number variations in cancer genome using next generation sequencing: principles and challengesZebrafish sex: a complicated affairGuidelines for the design, analysis and interpretation of 'omics' data: focus on human endometriumHidden Markov Model-Based CNV Detection Algorithms for Illumina Genotyping MicroarraysConnecting Anxiety and Genomic Copy Number Variation: A Genome-Wide Analysis in CD-1 MiceCopy number variations and strokeA copy number variation map of the human genomeDetectable clonal mosaicism from birth to old age and its relationship to cancerTranscriptome sequencing of tumor subpopulations reveals a spectrum of therapeutic options for squamous cell lung cancerRare Copy Number Variants Identified Suggest the Regulating Pathways in Hypertension-Related Left Ventricular HypertrophyBurden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsiesNovel population specific autosomal copy number variation and its functional analysis amongst Negritos from Peninsular MalaysiaThe Growing Importance of CNVs: New Insights for Detection and Clinical InterpretationCNVs leading to fusion transcripts in individuals with autism spectrum disorderChromosomal variation in lymphoblastoid cell linesGenome-wide survey of large rare copy number variants in Alzheimer's disease among Caribbean hispanicsGenome-wide copy number variation analysis in extended families and unrelated individuals characterized for musical aptitude and creativity in music.The genome-wide landscape of copy number variations in the MUSGEN study provides evidence for a founder effect in the isolated Finnish population.Non-random DNA fragmentation in next-generation sequencing.Exploration of large, rare copy number variants associated with psychiatric and neurodevelopmental disorders in individuals with anorexia nervosa.Inheritance model introduces differential bias in CNV calls between parents and offspringA survey of copy-number variation detection tools based on high-throughput sequencing data.Effect of Combining Multiple CNV Defining Algorithms on the Reliability of CNV Calls from SNP Genotyping DataEnhancing systems medicine beyond genotype data by dynamic patient signatures: having information and using it tooCase report: whole exome sequencing of primary cardiac angiosarcoma highlights potential for targeted therapiesConcordance of copy number alterations using a common analytic pipeline for genome-wide analysis of Illumina and Affymetrix genotyping data: a report from the Children's Oncology Group.Evaluation of somatic copy number estimation tools for whole-exome sequencing data.A simplicial complex-based approach to unmixing tumor progression data.Medoidshift clustering applied to genomic bulk tumor data.DNA fragmentation simulation method (FSM) and fragment size matching improve aCGH performance of FFPE tissues.Copy number analysis of whole-genome data using BIC-seq2 and its application to detection of cancer susceptibility variants.Comparative Analysis of CNV Calling Algorithms: Literature Survey and a Case Study Using Bovine High-Density SNP DataGenome-wide copy number variant discovery in dogs using the CanineHD genotyping array.De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.
P2860
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P2860
Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants
description
2011 nî lūn-bûn
@nan
2011 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Comprehensive assessment of ar ...... ection of copy number variants
@ast
Comprehensive assessment of ar ...... ection of copy number variants
@en
Comprehensive assessment of ar ...... ection of copy number variants
@nl
type
label
Comprehensive assessment of ar ...... ection of copy number variants
@ast
Comprehensive assessment of ar ...... ection of copy number variants
@en
Comprehensive assessment of ar ...... ection of copy number variants
@nl
prefLabel
Comprehensive assessment of ar ...... ection of copy number variants
@ast
Comprehensive assessment of ar ...... ection of copy number variants
@en
Comprehensive assessment of ar ...... ection of copy number variants
@nl
P2093
P2860
P50
P3181
P356
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P1476
Comprehensive assessment of ar ...... ection of copy number variants
@en
P2093
Anath C Lionel
Charles Lee
Diana Rajan
Diane Rigler
Elena Prigmore
Ji Hyeon Park
Katayoon Darvishi
Kristin Noonan
Matthew E Hurles
P2860
P2888
P304
P3181
P356
10.1038/NBT.1852
P407
P50
P577
2011-05-08T00:00:00Z