CNAseg--a novel framework for identification of copy number changes in cancer from second-generation sequencing data.
about
GROM-RD: resolving genomic biases to improve read depth detection of copy number variantsCurrent challenges in the bioinformatics of single cell genomics.COPS: 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 perspectivesDetection of Genomic Structural Variants from Next-Generation Sequencing DataSummarizing and correcting the GC content bias in high-throughput sequencingParsimonious higher-order hidden Markov models for improved array-CGH analysis with applications to Arabidopsis thaliana.A survey of copy-number variation detection tools based on high-throughput sequencing data.Modeling read counts for CNV detection in 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.Comparative analysis of methods for identifying somatic copy number alterations from deep sequencing data.Identification of copy number variants in whole-genome data using Reference Coverage Profiles.G-CNV: A GPU-Based Tool for Preparing Data to Detect CNVs with Read-Depth Methods.Modeling the next generation sequencing read count data for DNA copy number variant study.CNV-CH: A Convex Hull Based Segmentation Approach to Detect Copy Number Variations (CNV) Using Next-Generation Sequencing Data.CRCDA--Comprehensive resources for cancer NGS data analysis.PSE-HMM: genome-wide CNV detection from NGS data using an HMM with Position-Specific Emission probabilities.Copy number variation detection using next generation sequencing read counts.Identification of structural variation in mouse genomes.cn.MOPS: mixture of Poissons for discovering copy number variations in next-generation sequencing data with a low false discovery rateCorrecting for cancer genome size and tumour cell content enables better estimation of copy number alterations from next-generation sequence data.Common copy number variation detection from multiple sequenced samplesCONTRA: copy number analysis for targeted resequencing.CoNVEX: copy number variation estimation in exome sequencing data using HMMRobust Detection and Identification of Sparse Segments in Ultra-High Dimensional Data Analysis.Comparative studies of copy number variation detection methods for next-generation sequencing technologiesCNV-TV: a robust method to discover copy number variation from short sequencing reads.Future medical applications of single-cell sequencing in cancer.A somatic reference standard for cancer genome sequencing.Copy number alterations detected by whole-exome and whole-genome sequencing of esophageal adenocarcinoma.Improving detection of copy-number variation by simultaneous bias correction and read-depth segmentationUse of autocorrelation scanning in DNA copy number analysis.Read count approach for DNA copy number variants detection.Technical and implementation issues in using next-generation sequencing of cancers in clinical practice.WaveCNV: allele-specific copy number alterations in primary tumors and xenograft models from next-generation sequencing.Whole-genome CNV analysis: advances in computational approachesA Total-variation Constrained Permutation Model for Revealing Common Copy Number Patterns.Clinical Applications of Next-Generation Sequencing in Cancer Diagnosis.PSCC: sensitive and reliable population-scale copy number variation detection method based on low coverage sequencing
P2860
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P2860
CNAseg--a novel framework for identification of copy number changes in cancer from second-generation sequencing data.
description
2010 nî lūn-bûn
@nan
2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հոտեմբերին 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
CNAseg--a novel framework for ...... nd-generation sequencing data.
@ast
CNAseg--a novel framework for ...... nd-generation sequencing data.
@en
type
label
CNAseg--a novel framework for ...... nd-generation sequencing data.
@ast
CNAseg--a novel framework for ...... nd-generation sequencing data.
@en
prefLabel
CNAseg--a novel framework for ...... nd-generation sequencing data.
@ast
CNAseg--a novel framework for ...... nd-generation sequencing data.
@en
P2093
P2860
P356
P1433
P1476
CNAseg--a novel framework for ...... ond-generation sequencing data
@en
P2093
Dirk J Evers
R Keira Cheetham
Sergii Ivakhno
Simon Tavaré
P2860
P304
P356
10.1093/BIOINFORMATICS/BTQ587
P407
P577
2010-10-21T00:00:00Z