Statistical challenges associated with detecting copy number variations with next-generation sequencing.
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Computational tools for copy number variation (CNV) detection using next-generation sequencing data: features and perspectivesEstrogen receptor alpha gene amplification in breast cancer: 25 years of debateNovel bioinformatic developments for exome sequencingOverview of recurrent chromosomal losses in retinoblastoma detected by low coverage next generation sequencingStatistical analysis for genome-wide association studyComputational methods for detecting copy number variations in cancer genome using next generation sequencing: principles and challengesDetection of Genomic Structural Variants from Next-Generation Sequencing DataThe genetic basis of music abilitySomatiCA: identifying, characterizing and quantifying somatic copy number aberrations from cancer genome sequencing data.Prevention, diagnosis and treatment of high-throughput sequencing data pathologies.Parametric modeling of whole-genome sequencing data for CNV identification.Mining genome sequencing data to identify the genomic features linked to breast cancer histopathology.Identification of copy number variants in whole-genome data using Reference Coverage Profiles.Combined Analysis of SNP Array Data Identifies Novel CNV Candidates and Pathways in Ependymoma and MesotheliomaAnalysis of exome sequencing data sets reveals structural variation in the coding region of ABO in individuals of African ancestry.Homozygous and hemizygous CNV detection from exome sequencing data in a Mendelian disease cohort.Biological relevance of CNV calling methods using familial relatedness including monozygotic twins.seqCNA: an R package for DNA copy number analysis in cancer using high-throughput sequencing.SegAnnDB: interactive Web-based genomic segmentation.Good Laboratory Standards for Clinical Next-Generation Sequencing Cancer Panel Tests.An evaluation of copy number variation detection tools for cancer using whole exome sequencing data.ExCNVSS: A Noise-Robust Method for Copy Number Variation Detection in Whole Exome Sequencing Data.Common copy number variation detection from multiple sequenced samplesGenome-wide patterns of copy number variation in the diversified chicken genomes using next-generation sequencingDNA copy number analysis of fresh and formalin-fixed specimens by shallow whole-genome sequencing with identification and exclusion of problematic regions in the genome assembly.Dynamics of copy number variation in host races of the pea aphid.Copy number variation analysis based on AluScan sequencesESR1 amplification in breast cancer by optimized RNase FISH: frequent but low-level and heterogeneous.Improved molecular diagnosis by the detection of exonic deletions with target gene capture and deep sequencing.CODOC: efficient access, analysis and compression of depth of coverage signals.Sequence variation within the KIV-2 copy number polymorphism of the human LPA gene in African, Asian, and European populations.Quantitative analysis of differences in copy numbers using read depth obtained from PCR-enriched samples and controls.Comparison of sequencing based CNV discovery methods using monozygotic twin quartets.Identifying Human Genome-Wide CNV, LOH and UPD by Targeted Sequencing of Selected Regions.TAFFYS: An Integrated Tool for Comprehensive Analysis of Genomic Aberrations in Tumor Samples.One CNV Discordance in NRXN1 Observed Upon Genome-wide Screening in 38 Pairs of Adult Healthy Monozygotic Twins.Copy number variants in the sheep genome detected using multiple approachesBetween-species differences in gene copy number are enriched among functions critical for adaptive evolution in Arabidopsis halleri.CNV discovery for milk composition traits in dairy cattle using whole genome resequencing.A rapid NGS strategy for comprehensive molecular diagnosis of Birt-Hogg-Dubé syndrome in patients with primary spontaneous pneumothorax
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P2860
Statistical challenges associated with detecting copy number variations with next-generation sequencing.
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
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artigo científico
@pt-br
artikel ilmiah
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artikull shkencor
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artículo científico
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name
Statistical challenges associa ...... th next-generation sequencing.
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type
label
Statistical challenges associa ...... th next-generation sequencing.
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prefLabel
Statistical challenges associa ...... th next-generation sequencing.
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P2093
P2860
P356
P1433
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Statistical challenges associa ...... ith next-generation sequencing
@en
P2093
Chee Seng Ku
Kee Seng Chia
Yudi Pawitan
P2860
P304
P356
10.1093/BIOINFORMATICS/BTS535
P407
P577
2012-08-31T00:00:00Z