STAC: A method for testing the significance of DNA copy number aberrations across multiple array-CGH experiments. - Wikidata - awgldk - TriplyDB

STAC: A method for testing the significance of DNA copy number aberrations across multiple array-CGH experiments.

STAC: A method for testing the significance of DNA copy number aberrations across multiple array-CGH experiments.

http://www.wikidata.org/entity/Q30821792

about

Detecting statistically significant common insertion sites in retroviral insertional mutagenesis screens Genome-wide copy number profiling on high-density bacterial artificial chromosomes, single-nucleotide polymorphisms, and oligonucleotide microarrays: a platform comparison based on statistical power analysis Genomic aberrations in lung adenocarcinoma in never smokers Flexible and accurate detection of genomic copy-number changes from aCGH.DiNAMIC: a method to identify recurrent DNA copy number aberrations in tumors Multisample aCGH data analysis via total variation and spectral regularization.Identification of cancer genes using a statistical framework for multiexperiment analysis of nondiscretized array CGH data.Assessing the significance of conserved genomic aberrations using high resolution genomic microarrays.Genome-wide genetic aberrations of thymoma using cDNA microarray based comparative genomic hybridization.SIRAC: Supervised Identification of Regions of Aberration in aCGH datasets.Functional copy-number alterations in cancer.Experimental design and data analysis for array comparative genomic hybridization.Exploratory analysis of the copy number alterations in glioblastoma multiforme.Markov Models for inferring copy number variations from genotype data on Illumina platforms High-resolution analysis of copy number alterations and associated expression changes in ovarian tumors.CGHregions: dimension reduction for array CGH data with minimal information loss Model-based clustering of array CGH data.A Bayesian approach to efficient differential allocation for resampling-based significance testing.Finding exclusively deleted or amplified genomic areas in lung adenocarcinomas using a novel chromosomal pattern analysis Analysis of array-CGH data using the R and Bioconductor software suite.CMDS: a population-based method for identifying recurrent DNA copy number aberrations in cancer from high-resolution data.Identification of recurrent regions of Copy-Number Variants across multiple individuals.Integrated high-resolution array CGH and SKY analysis of homozygous deletions and other genomic alterations present in malignant mesothelioma cell lines.Detecting independent and recurrent copy number aberrations using interval graphs.Accuracy of CNV Detection from GWAS Data.Detection of recurrent rearrangement breakpoints from copy number data Bayesian Random Segmentation Models to Identify Shared Copy Number Aberrations for Array CGH Data Wavelet-based identification of DNA focal genomic aberrations from single nucleotide polymorphism arrays.A fused lasso latent feature model for analyzing multi-sample aCGH data waviCGH: a web application for the analysis and visualization of genomic copy number alterations.A multi-sample based method for identifying common CNVs in normal human genomic structure using high-resolution aCGH data Discovering tumor suppressor genes through genome-wide copy number analysis.Highly aneuploid zebrafish malignant peripheral nerve sheath tumors have genetic alterations similar to human cancers.Mesenchymal transition and PDGFRA amplification/mutation are key distinct oncogenic events in pediatric diffuse intrinsic pontine gliomas.Identification of differential aberrations in multiple-sample array CGH studies TAGCNA: a method to identify significant consensus events of copy number alterations in cancer.Genome-wide identification of significant aberrations in cancer genome.A comprehensive characterization of genome-wide copy number aberrations in colorectal cancer reveals novel oncogenes and patterns of alterations Gender-associated genomic differences in colorectal cancer: clinical insight from feminization of male cancer cells.ROCK1 as a novel prognostic marker in vulvar cancer

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STAC: A method for testing the significance of DNA copy number aberrations across multiple array-CGH experiments.

http://www.wikidata.org/entity/Q30821792

description

2006 nî lūn-bûn

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2006 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2006 թվականի օգոստոսին հրատարակված գիտական հոդված

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年论文

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Barbara L Weber

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Christian J Stoeckert

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Joel Greshock

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John M Maris

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Yael P Mosse

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1-Mb resolution array-based comparative genomic hybridization using a BAC clone set optimized for cancer gene analysis

Cluster analysis and display of genome-wide expression patterns

High resolution genomic analysis of sporadic breast cancer using array-based comparative genomic hybridization

EGFR mutations in lung cancer: correlation with clinical response to gefitinib therapy.

Activating mutations in the epidermal growth factor receptor underlying responsiveness of non-small-cell lung cancer to gefitinib

Segmental duplications and copy-number variation in the human genome.

High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays

Recent segmental duplications in the human genome

A comparison study: applying segmentation to array CGH data for downstream analyses.

Comparative analysis of algorithms for identifying amplifications and deletions in array CGH data.

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Gregory R Grant

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