CODEX: a normalization and copy number variation detection method for whole exome sequencing.
about
Novel bioinformatic developments for exome sequencingDetection of Genomic Structural Variants from Next-Generation Sequencing DataCoNVaDING: Single Exon Variation Detection in Targeted NGS Data.Enhanced copy number variants detection from whole-exome sequencing data using EXCAVATOR2Homozygous and hemizygous CNV detection from exome sequencing data in a Mendelian disease cohort.Research progress of neuroblastoma related gene variations.Gene-based comparative analysis of tools for estimating copy number alterations using whole-exome sequencing data.The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk.Korean Variant Archive (KOVA): a reference database of genetic variations in the Korean population.CNVkit: Genome-Wide Copy Number Detection and Visualization from Targeted DNA Sequencing.Comparison of the Lonidamine Potentiated Effect of Nitrogen Mustard Alkylating Agents on the Systemic Treatment of DB-1 Human Melanoma Xenografts in MiceTargeted capture in evolutionary and ecological genomics.Assessing the reproducibility of exome copy number variations predictions.Whole-exome sequencing in the molecular diagnosis of individuals with congenital anomalies of the kidney and urinary tract and identification of a new causative gene.SynthEx: a synthetic-normal-based DNA sequencing tool for copy number alteration detection and tumor heterogeneity profiling.Exome sequencing of oral squamous cell carcinoma in users of Arabian snuff reveals novel candidates for driver genes.Heterozygous HNRNPU variants cause early onset epilepsy and severe intellectual disability.ALLELE-SPECIFIC COPY NUMBER ESTIMATION BY WHOLE EXOME SEQUENCING.Genetic and Genomic Characterization of 462 Melanoma Patient-Derived Xenografts, Tumor Biopsies, and Cell Lines.WISExome: a within-sample comparison approach to detect copy number variations in whole exome sequencing data.Sensitivity of whole exome sequencing in detecting infantile- and late-onset Pompe disease.Accounting for GC-content bias reduces systematic errors and batch effects in ChIP-seq data.A randomized approach to speed up the analysis of large-scale read-count data in the application of CNV detection.Whole-exome sequencing identifies novel pathogenic mutations and putative phenotype-influencing variants in Polish limb-girdle muscular dystrophy patients.Ximmer: A system for improving accuracy and consistency of CNV calling from exome dataDeviCNV: detection and visualization of exon-level copy number variants in targeted next-generation sequencing data
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P2860
CODEX: a normalization and copy number variation detection method for whole exome sequencing.
description
2015 nî lūn-bûn
@nan
2015 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2015年の論文
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2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
CODEX: a normalization and cop ...... od for whole exome sequencing.
@ast
CODEX: a normalization and cop ...... od for whole exome sequencing.
@en
type
label
CODEX: a normalization and cop ...... od for whole exome sequencing.
@ast
CODEX: a normalization and cop ...... od for whole exome sequencing.
@en
prefLabel
CODEX: a normalization and cop ...... od for whole exome sequencing.
@ast
CODEX: a normalization and cop ...... od for whole exome sequencing.
@en
P2093
P2860
P356
P1476
CODEX: a normalization and cop ...... od for whole exome sequencing.
@en
P2093
Derek A Oldridge
Nancy R Zhang
Sharon J Diskin
P2860
P356
10.1093/NAR/GKU1363
P407
P50
P577
2015-01-23T00:00:00Z