Comparative analyses of seven algorithms for copy number variant identification from single nucleotide polymorphism arrays.
about
Detectable clonal mosaicism and its relationship to aging and cancerHidden Markov Model-Based CNV Detection Algorithms for Illumina Genotyping MicroarraysIntegration of transcript expression, copy number and LOH analysis of infiltrating ductal carcinoma of the breastComprehensive assessment of array-based platforms and calling algorithms for detection of copy number variantsComparative analysis of copy number variation detection methods and database constructionMassive screening of copy number population-scale variation in Bos taurus genomeGenome-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.Rapid visualisation of microarray copy number data for the detection of structural variations linked to a disease phenotypeEffect of Combining Multiple CNV Defining Algorithms on the Reliability of CNV Calls from SNP Genotyping DataContinuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients.Comparative Analysis of CNV Calling Algorithms: Literature Survey and a Case Study Using Bovine High-Density SNP DataIncreased CNV-region deletions in mild cognitive impairment (MCI) and Alzheimer's disease (AD) subjects in the ADNI sampleCopy number variation in the porcine genome inferred from a 60 k SNP BeadChipAnalysis of copy loss and gain variations in Holstein cattle autosomes using BeadChip SNPsExpanding the genetic basis of copy number variation in familial breast cancer.Absence/presence calling in microarray-based CGH experiments with non-model organismscn.FARMS: a latent variable model to detect copy number variations in microarray data with a low false discovery rate.Detection of genome-wide copy number variations in two chicken lines divergently selected for abdominal fat content.Genomic profiling by whole-genome single nucleotide polymorphism arrays in Wilms tumor and association with relapse.Change-point analysis of paired allele-specific copy number variation data.Identification and validation of copy number variants using SNP genotyping arrays from a large clinical cohortUsing family data as a verification standard to evaluate copy number variation calling strategies for genetic association studiesGenome-wide CNV analysis replicates the association between GSTM1 deletion and bladder cancer: a support for using continuous measurement from SNP-array dataStructural architecture of SNP effects on complex traits.Fast detection of de novo copy number variants from SNP arrays for case-parent trios.Genetic copy number variation and general cognitive abilityAnalysis of copy number variations in the sheep genome using 50K SNP BeadChip arrayDNA copy number variants of known glaucoma genes in relation to primary open-angle glaucomaGenetic Analyses of a Three Generation Family Segregating Hirschsprung Disease and Iris Heterochromia.Analysis of copy number variants by three detection algorithms and their association with body size in horses.Genomic Copy Number Analysis in Alzheimer's Disease and Mild Cognitive Impairment: An ADNI StudyGenome-scale analysis of replication timing: from bench to bioinformatics.Genome wide analysis reveals single nucleotide polymorphisms associated with fatness and putative novel copy number variants in three pig breeds.Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patients.Copy number variation accuracy in genome-wide association studies.Assessment of copy number variation using the Illumina Infinium 1M SNP-array: a comparison of methodological approaches in the Spanish Bladder Cancer/EPICURO study.Genomic population structure and prevalence of copy number variations in South African Nguni cattle.An integrated analysis tool for analyzing hybridization intensities and genotypes using new-generation population-optimized human arrays.CNV analysis in the Lithuanian population.
P2860
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P2860
Comparative analyses of seven algorithms for copy number variant identification from single nucleotide polymorphism arrays.
description
2010 nî lūn-bûn
@nan
2010 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի փետրվարին 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
Comparative analyses of seven ...... ucleotide polymorphism arrays.
@ast
Comparative analyses of seven ...... ucleotide polymorphism arrays.
@en
type
label
Comparative analyses of seven ...... ucleotide polymorphism arrays.
@ast
Comparative analyses of seven ...... ucleotide polymorphism arrays.
@en
prefLabel
Comparative analyses of seven ...... ucleotide polymorphism arrays.
@ast
Comparative analyses of seven ...... ucleotide polymorphism arrays.
@en
P2093
P2860
P50
P356
P1476
Comparative analyses of seven ...... ucleotide polymorphism arrays.
@en
P2093
Andrew E Dellinger
Liang K Goh
Terri L Young
P2860
P356
10.1093/NAR/GKQ040
P407
P577
2010-02-08T00:00:00Z