Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNV
about
GROM-RD: resolving genomic biases to improve read depth detection of copy number variantsCOPS: a sensitive and accurate tool for detecting somatic Copy Number Alterations using short-read sequence data from paired samplesComputational tools for copy number variation (CNV) detection using next-generation sequencing data: features and perspectivesSingle-cell sequencing analysis characterizes common and cell-lineage-specific mutations in a muscle-invasive bladder cancerExome sequencing identifies recurrent somatic RAC1 mutations in melanomaA genetic model for neurodevelopmental diseaseComputational methods for detecting copy number variations in cancer genome using next generation sequencing: principles and challengesDetection of Genomic Structural Variants from Next-Generation Sequencing DataDetectable clonal mosaicism in the human genomeHigh-resolution mutational profiling suggests the genetic validity of glioblastoma patient-derived pre-clinical modelsAtaxia and hypogonadism caused by the loss of ubiquitin ligase activity of the U box protein CHIPCopy number variation detection and genotyping from exome sequence data.A robust model for read count data in exome sequencing experiments and implications for copy number variant callingA survey of copy-number variation detection tools based on high-throughput sequencing data.Modeling read counts for CNV detection in exome sequencing data.Copy Number Variation detection from 1000 Genomes Project exon capture sequencing data.Estimation of copy number alterations from exome sequencing data.CEQer: a graphical tool for copy number and allelic imbalance detection from whole-exome sequencing data.SomatiCA: identifying, characterizing and quantifying somatic copy number aberrations from cancer genome sequencing data.Detection of structural DNA variation from next generation sequencing data: a review of informatic approaches.Identification of novel point mutations in splicing sites integrating whole-exome and RNA-seq data in myeloproliferative diseasesComparative analysis of methods for identifying somatic copy number alterations from deep sequencing data.Using XHMM Software to Detect Copy Number Variation in Whole-Exome Sequencing Data.CANOES: detecting rare copy number variants from whole exome sequencing data.CLImAT: accurate detection of copy number alteration and loss of heterozygosity in impure and aneuploid tumor samples using whole-genome sequencing data.PatternCNV: a versatile tool for detecting copy number changes from exome sequencing data.Multi-factor data normalization enables the detection of copy number aberrations in amplicon sequencing data.Identification of copy number variants from exome sequence data.cnvOffSeq: detecting intergenic copy number variation using off-target exome sequencing dataInferring copy number and genotype in tumour exome data.cnvCapSeq: detecting copy number variation in long-range targeted resequencing data.ExomeAI: detection of recurrent allelic imbalance in tumors using whole-exome sequencing data.Quantifying tumor heterogeneity in whole-genome and whole-exome sequencing data.CopywriteR: DNA copy number detection from off-target sequence dataDeAnnCNV: a tool for online detection and annotation of copy number variations from whole-exome sequencing dataEvaluation of somatic copy number estimation tools for whole-exome sequencing data.A Sparse Model Based Detection of Copy Number Variations From Exome Sequencing DataBubbleTree: an intuitive visualization to elucidate tumoral aneuploidy and clonality using next generation sequencing data.SAAS-CNV: A Joint Segmentation Approach on Aggregated and Allele Specific Signals for the Identification of Somatic Copy Number Alterations with Next-Generation Sequencing Data.VisCap: inference and visualization of germ-line copy-number variants from targeted clinical sequencing data.
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P2860
Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNV
description
2011 nî lūn-bûn
@nan
2011 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի օգոստոսին 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
Exome sequencing-based copy-nu ...... rozygosity detection: ExomeCNV
@ast
Exome sequencing-based copy-nu ...... rozygosity detection: ExomeCNV
@en
type
label
Exome sequencing-based copy-nu ...... rozygosity detection: ExomeCNV
@ast
Exome sequencing-based copy-nu ...... rozygosity detection: ExomeCNV
@en
prefLabel
Exome sequencing-based copy-nu ...... rozygosity detection: ExomeCNV
@ast
Exome sequencing-based copy-nu ...... rozygosity detection: ExomeCNV
@en
P2093
P2860
P356
P1433
P1476
Exome sequencing-based copy-nu ...... rozygosity detection: ExomeCNV
@en
P2093
Alistair J Cochran
Basil A J Horst
Georg Brunner
Jarupon Fah Sathirapongsasuti
Scott Binder
Stanley F Nelson
P2860
P304
P356
10.1093/BIOINFORMATICS/BTR462
P407
P577
2011-08-09T00:00:00Z