Allele-specific amplification in cancer revealed by SNP array analysis
about
Tumor transcriptome sequencing reveals allelic expression imbalances associated with copy number alterationsFunctional polymorphism of the CK2alpha intronless gene plays oncogenic roles in lung cancerThe application of single nucleotide polymorphism microarrays in cancer researchCARAT: a novel method for allelic detection of DNA copy number changes using high density oligonucleotide arrays.Genome wide SNP comparative analysis between EGFR and KRAS mutated NSCLC and characterization of two models of oncogenic cooperation in non-small cell lung carcinomaThe Growing Importance of CNVs: New Insights for Detection and Clinical InterpretationQuantification of normal cell fraction and copy number neutral LOH in clinical lung cancer samples using SNP array dataA Hidden Markov Model to estimate population mixture and allelic copy-numbers in cancers using Affymetrix SNP arrays.Mismatch and G-stack modulated probe signals on SNP microarrays.QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data.Assessment of algorithms for high throughput detection of genomic copy number variation in oligonucleotide microarray data.A molecular scheme for improved characterization of human embryonic stem cell linesToward accurate high-throughput SNP genotyping in the presence of inherited copy number variation.SNPExpress: integrated visualization of genome-wide genotypes, copy numbers and gene expression levels.Major copy proportion analysis of tumor samples using SNP arrays.An integrated epigenetic and genetic analysis of DNA methyltransferase genes (DNMTs) in tumor resistant and susceptible chicken lines.Assessing batch effects of genotype calling algorithm BRLMM for the Affymetrix GeneChip Human Mapping 500 K array set using 270 HapMap samples.Estimation of tumor heterogeneity using CGH array data.Oncogene mutations, copy number gains and mutant allele specific imbalance (MASI) frequently occur together in tumor cells.PICNIC: 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 microarraysAn integrated Bayesian analysis of LOH and copy number data.Allelic selection of amplicons in glioblastoma revealed by combining somatic and germline analysis.A statistical approach for detecting genomic aberrations in heterogeneous tumor samples from single nucleotide polymorphism genotyping dataEstimation of parent specific DNA copy number in tumors using high-density genotyping arrays.Making sense of cancer genomic data.Network-guided analysis of genes with altered somatic copy number and gene expression reveals pathways commonly perturbed in metastatic melanoma.Calling amplified haplotypes in next generation tumor sequence data.Common alleles in candidate susceptibility genes associated with risk and development of epithelial ovarian cancer.Identification and validation of copy number variants using SNP genotyping arrays from a large clinical cohortMutation discovery in regions of segmental cancer genome amplifications with CoNAn-SNV: a mixture model for next generation sequencing of tumorsHuman spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1.Differences help recognition: a probabilistic interpretationMicroarray MAPH: accurate array-based detection of relative copy number in genomic DNA.Cancer gene discovery in mouse and man.A Likelihood-Based Framework for Association Analysis of Allele-Specific Copy Numbers.Parent-specific copy number in paired tumor-normal studies using circular binary segmentationGenome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays.DNA copy number variation and loss of heterozygosity in relation to recurrence of and survival from head and neck squamous cell carcinoma: a review.Genome-Wide Loss of Heterozygosity and DNA Copy Number Aberration in HPV-Negative Oral Squamous Cell Carcinoma and Their Associations with Disease-Specific Survival.
P2860
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P2860
Allele-specific amplification in cancer revealed by SNP array analysis
description
2005 nî lūn-bûn
@nan
2005 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Allele-specific amplification in cancer revealed by SNP array analysis
@ast
Allele-specific amplification in cancer revealed by SNP array analysis
@en
Allele-specific amplification in cancer revealed by SNP array analysis
@nl
type
label
Allele-specific amplification in cancer revealed by SNP array analysis
@ast
Allele-specific amplification in cancer revealed by SNP array analysis
@en
Allele-specific amplification in cancer revealed by SNP array analysis
@nl
prefLabel
Allele-specific amplification in cancer revealed by SNP array analysis
@ast
Allele-specific amplification in cancer revealed by SNP array analysis
@en
Allele-specific amplification in cancer revealed by SNP array analysis
@nl
P2093
P2860
P1476
Allele-specific amplification in cancer revealed by SNP array analysis
@en
P2093
Barbara A Weir
David Harrington
Rameen Beroukhim
Thomas LaFramboise
William R Sellers
Xiaojun Zhao
P2860
P356
10.1371/JOURNAL.PCBI.0010065
P407
P577
2005-11-25T00:00:00Z