An integrated view of copy number and allelic alterations in the cancer genome using single nucleotide polymorphism arrays.
about
Inferring loss-of-heterozygosity from unpaired tumors using high-density oligonucleotide SNP arraysHomozygously deleted gene DACH1 regulates tumor-initiating activity of glioma cellsMutations in DCPS and EDC3 in autosomal recessive intellectual disability indicate a crucial role for mRNA decapping in neurodevelopmentIncreased copy number at 3p14 in breast cancerAllele quantification using molecular inversion probes (MIP).Genomic representations using concatenates of Type IIB restriction endonuclease digestion fragmentsCaSNP: a database for interrogating copy number alterations of cancer genome from SNP array dataAnalysis 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 tumorsA collection of breast cancer cell lines for the study of functionally distinct cancer subtypesCharacterizing the cancer genome in lung adenocarcinoma.Impact of whole genome amplification on analysis of copy number variantsCC2D2A, encoding a coiled-coil and C2 domain protein, causes autosomal-recessive mental retardation with retinitis pigmentosaStructural variation of chromosomes in autism spectrum disorderHighly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarraysA haplotype map of the human genomeAllele-specific amplification in cancer revealed by SNP array analysisAnalysis and visualization of chromosomal abnormalities in SNP data with SNPscanBAC to the future! or oligonucleotides: a perspective for micro array comparative genomic hybridization (array CGH)Integrating genetics and epigenetics in breast cancer: biological insights, experimental, computational methods and therapeutic potentialA systematic comparison of copy number alterations in four types of female cancerFast Bayesian Inference of Copy Number Variants using Hidden Markov Models with Wavelet CompressionSNP microarray analyses reveal copy number alterations and progressive genome reorganization during tumor development in SVT/t driven mice breast cancerSNP and gene networks construction and analysis from classification of copy number variations dataQuantification of normal cell fraction and copy number neutral LOH in clinical lung cancer samples using SNP array dataAutomating dChip: toward reproducible sharing of microarray data analysisA genome-wide screen for microdeletions reveals disruption of polarity complex genes in diverse human cancersConcurrent loss of heterozygosity and copy number analysis in adenoid cystic carcinoma by SNP genotyping arrays.Parsimonious higher-order hidden Markov models for improved array-CGH analysis with applications to Arabidopsis thaliana.DiNAMIC: a method to identify recurrent DNA copy number aberrations in tumorsRapid visualisation of microarray copy number data for the detection of structural variations linked to a disease phenotypeProgenetix: 12 years of oncogenomic data curation.A Hidden Markov Model to estimate population mixture and allelic copy-numbers in cancers using Affymetrix SNP arrays.Outlier reset CUSUM for the exploration of copy number alteration data.Bayesian estimation of genomic copy number with single nucleotide polymorphism genotyping arraysQuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data.ADaCGH: A parallelized web-based application and R package for the analysis of aCGH data.Assessment of algorithms for high throughput detection of genomic copy number variation in oligonucleotide microarray data.Sparse representation and Bayesian detection of genome copy number alterations from microarray data.wuHMM: a robust algorithm to detect DNA copy number variation using long oligonucleotide microarray data
P2860
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P2860
An integrated view of copy number and allelic alterations in the cancer genome using single nucleotide polymorphism arrays.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
An integrated view of copy num ...... ucleotide polymorphism arrays.
@en
type
label
An integrated view of copy num ...... ucleotide polymorphism arrays.
@en
prefLabel
An integrated view of copy num ...... ucleotide polymorphism arrays.
@en
P2093
P1433
P1476
An integrated view of copy num ...... ucleotide polymorphism arrays.
@en
P2093
David Christiani
J Guillermo Paez
Joe W Gray
John Minna
Luc Girard
Tzu-Hsiu Chen
William R Sellers
P304
P356
10.1158/0008-5472.CAN-03-3308
P407
P577
2004-05-01T00:00:00Z