Major copy proportion analysis of tumor samples using SNP arrays.
about
Two-round coamplification at lower denaturation temperature-PCR (COLD-PCR)-based sanger sequencing identifies a novel spectrum of low-level mutations in lung adenocarcinomaSubcloneSeeker: a computational framework for reconstructing tumor clone structure for cancer variant interpretation and prioritization.An assessment of computational methods for estimating purity and clonality using genomic data derived from heterogeneous tumor tissue samplesPICNIC: an algorithm to predict absolute allelic copy number variation with microarray cancer data.TumorBoost: normalization of allele-specific tumor copy numbers from a single pair of tumor-normal genotyping microarraysMixHMM: inferring copy number variation and allelic imbalance using SNP arrays and tumor samples mixed with stromal cellsGenome Alteration Print (GAP): a tool to visualize and mine complex cancer genomic profiles obtained by SNP arrays.A new analysis tool for individual-level allele frequency for genomic studies.Computational analysis of whole-genome differential allelic expression data in human.Estimation of parent specific DNA copy number in tumors using high-density genotyping arrays.Model-integrated estimation of normal tissue contamination for cancer SNP allelic copy number data.Profiles of genomic instability in high-grade serous ovarian cancer predict treatment outcomeParadoxical relationship between chromosomal instability and survival outcome in cancer.Parent-specific copy number in paired tumor-normal studies using circular binary segmentationRelationship of extreme chromosomal instability with long-term survival in a retrospective analysis of primary breast cancerAn integrated analysis tool for analyzing hybridization intensities and genotypes using new-generation population-optimized human arrays.Getting DNA copy numbers without control samples.Segmentation-based detection of allelic imbalance and loss-of-heterozygosity in cancer cells using whole genome SNP arrays.The Role of Constitutional Copy Number Variants in Breast Cancer.Use of autocorrelation scanning in DNA copy number analysis.Single nucleotide polymorphism arrays: a decade of biological, computational and technological advances.Comparing CNV detection methods for SNP arrays.Loss of heterozygosity analysis in malignant gliomas.Sexual dimorphism in glioma glycolysis underlies sex differences in survivalAllele-specific copy number analysis of tumor samples with aneuploidy and tumor heterogeneityLOHAS: loss-of-heterozygosity analysis suite.Allele-specific copy number profiling by next-generation DNA sequencingAmerican Association for Cancer Research Genetics and Biology of Brain Cancers 2009, December 13-15, 2009, San Diego, CA.
P2860
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P2860
Major copy proportion analysis of tumor samples using SNP arrays.
description
2008 nî lūn-bûn
@nan
2008 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Major copy proportion analysis of tumor samples using SNP arrays.
@ast
Major copy proportion analysis of tumor samples using SNP arrays.
@en
Major copy proportion analysis of tumor samples using SNP arrays.
@nl
type
label
Major copy proportion analysis of tumor samples using SNP arrays.
@ast
Major copy proportion analysis of tumor samples using SNP arrays.
@en
Major copy proportion analysis of tumor samples using SNP arrays.
@nl
prefLabel
Major copy proportion analysis of tumor samples using SNP arrays.
@ast
Major copy proportion analysis of tumor samples using SNP arrays.
@en
Major copy proportion analysis of tumor samples using SNP arrays.
@nl
P2093
P2860
P50
P356
P1433
P1476
Major copy proportion analysis of tumor samples using SNP arrays.
@en
P2093
Barbara A Weir
Rameen Beroukhim
William R Sellers
P2860
P2888
P356
10.1186/1471-2105-9-204
P577
2008-04-21T00:00:00Z
P5875
P6179
1038304946