Comparative study of exome copy number variation estimation tools using array comparative genomic hybridization as control.
about
SciClone: inferring clonal architecture and tracking the spatial and temporal patterns of tumor evolutionEvaluation of somatic copy number estimation tools for whole-exome sequencing data.arrEYE: a customized platform for high-resolution copy number analysis of coding and noncoding regions of known and candidate retinal dystrophy genes and retinal noncoding RNAs.The validation and clinical implementation of BRCAplus: a comprehensive high-risk breast cancer diagnostic assay.Gene-based comparative analysis of tools for estimating copy number alterations using whole-exome sequencing data.Current status of comprehensive chromosome screening for elective single-embryo transfer.An evaluation of copy number variation detection tools from whole-exome sequencing data.Detection of internal exon deletion with exon Del.Combined Targeted DNA Sequencing in Non-Small Cell Lung Cancer (NSCLC) Using UNCseq and NGScopy, and RNA Sequencing Using UNCqeR for the Detection of Genetic Aberrations in NSCLC.Allele-specific copy-number discovery from whole-genome and whole-exome sequencingCopy number alterations detected by whole-exome and whole-genome sequencing of esophageal adenocarcinoma.panelcn.MOPS: Copy-number detection in targeted NGS panel data for clinical diagnostics.Reliability of algorithmic somatic copy number alteration detection from targeted capture data.Assessing the reproducibility of exome copy number variations predictions.Evolutionary and Functional Features of Copy Number Variation in the Cattle Genome.Evaluation of three read-depth based CNV detection tools using whole-exome sequencing dataCertified DNA Reference Materials to Compare HER2 Gene Amplification Measurements Using Next-Generation Sequencing Methods.Application of whole-exome sequencing for detecting copy number variants in CMT1A/HNPP.Corrigendum to "Comparative Study of Exome Copy Number Variation Estimation Tools Using Array Comparative Genomic Hybridization as Control".Onco-proteogenomics: Multi-omics level data integration for accurate phenotype prediction.Ximmer: A system for improving accuracy and consistency of CNV calling from exome dataDetecting Copy Number Variation via Next Generation Technology
P2860
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P2860
Comparative study of exome copy number variation estimation tools using array comparative genomic hybridization as control.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
Comparative study of exome cop ...... omic hybridization as control.
@en
Comparative study of exome cop ...... omic hybridization as control.
@nl
type
label
Comparative study of exome cop ...... omic hybridization as control.
@en
Comparative study of exome cop ...... omic hybridization as control.
@nl
prefLabel
Comparative study of exome cop ...... omic hybridization as control.
@en
Comparative study of exome cop ...... omic hybridization as control.
@nl
P2093
P2860
P50
P356
P1476
Comparative study of exome cop ...... omic hybridization as control.
@en
P2093
Jennifer Pietenpol
Joshua A Bauer
P2860
P304
P356
10.1155/2013/915636
P407
P577
2013-11-04T00:00:00Z