High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping.
about
A complex genomic rearrangement involving the endothelin 3 locus causes dermal hyperpigmentation in the chickenDetectable clonal mosaicism and its relationship to aging and cancerUnderstanding the development of human bladder cancer by using a whole-organ genomic mapping strategyDistant metastasis occurs late during the genetic evolution of pancreatic cancerAnalysis of molecular inversion probe performance for allele copy number determinationGenomic analysis using high-density single nucleotide polymorphism-based oligonucleotide arrays and multiplex ligation-dependent probe amplification provides a comprehensive analysis of INI1/SMARCB1 in malignant rhabdoid tumorsIntegrated analysis of homozygous deletions, focal amplifications, and sequence alterations in breast and colorectal cancersRecurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypesHighly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarraysHidden Markov Model-Based CNV Detection Algorithms for Illumina Genotyping MicroarraysDevelopment of personalized tumor biomarkers using massively parallel sequencingDetection of chromosomal alterations in the circulation of cancer patients with whole-genome sequencingGenome-wide copy number profiling on high-density bacterial artificial chromosomes, single-nucleotide polymorphisms, and oligonucleotide microarrays: a platform comparison based on statistical power analysisSensitive and specific detection of mosaic chromosomal abnormalities using the Parent-of-Origin-based Detection (POD) methodGenomic aberrations in lung adenocarcinoma in never smokersDetectable clonal mosaicism from birth to old age and its relationship to cancerMosaic structural variation in children with developmental disordersMosaic loss of chromosome Y is associated with common variation near TCL1ARare Germline Copy Number Variations and Disease Susceptibility in Familial MelanomaA genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin doseSNP and gene networks construction and analysis from classification of copy number variations dataGenome-wide profiling of structural genomic variations in Korean HapMap individualsQuantification of normal cell fraction and copy number neutral LOH in clinical lung cancer samples using SNP array dataA genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagusPennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping dataMultidimensional gene set analysis of genomic dataQuality control and quality assurance in genotypic data for genome-wide association studies.Inheritance model introduces differential bias in CNV calls between parents and offspringIncreased LIS1 expression affects human and mouse brain developmentCLImAT: accurate detection of copy number alteration and loss of heterozygosity in impure and aneuploid tumor samples using whole-genome sequencing data.Quantitative analysis of low-density SNP data for parentage assignment and estimation of family contributions to pooled samples.Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization.The role of copy number variation in susceptibility to amyotrophic lateral sclerosis: genome-wide association study and comparison with published loci.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.A new molecular signature method for prediction of driver cancer pathways from transcriptional data.A Method for Checking Genomic Integrity in Cultured Cell Lines from SNP Genotyping Data.QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data.CloneCNA: detecting subclonal somatic copy number alterations in heterogeneous tumor samples from whole-exome sequencing dataSiDCoN: a tool to aid scoring of DNA copy number changes in SNP chip dataSparse representation and Bayesian detection of genome copy number alterations from microarray data.
P2860
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P2860
High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping.
description
2006 nî lūn-bûn
@nan
2006 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
High-resolution genomic profil ...... inium whole-genome genotyping.
@ast
High-resolution genomic profil ...... inium whole-genome genotyping.
@en
type
label
High-resolution genomic profil ...... inium whole-genome genotyping.
@ast
High-resolution genomic profil ...... inium whole-genome genotyping.
@en
prefLabel
High-resolution genomic profil ...... inium whole-genome genotyping.
@ast
High-resolution genomic profil ...... inium whole-genome genotyping.
@en
P2093
P2860
P356
P1433
P1476
High-resolution genomic profil ...... inium whole-genome genotyping.
@en
P2093
Daniel A Peiffer
David L Barker
Francisco Garcia
Frank J Steemers
Jennie M Le
Jiangzhen Li
Kevin L Gunderson
Kirt Haden
Richard M Shen
Sau Wai Cheung
P2860
P304
P356
10.1101/GR.5402306
P577
2006-08-09T00:00:00Z