Computation of recurrent minimal genomic alterations from array-CGH data.
about
Flexible and accurate detection of genomic copy-number changes from aCGH.STAC: A method for testing the significance of DNA copy number aberrations across multiple array-CGH experiments.Risk of hormone escape in a human prostate cancer model depends on therapy modalities and can be reduced by tyrosine kinase inhibitorsMarkers improve clustering of CGH data.ACTuDB, a new database for the integrated analysis of array-CGH and clinical data for tumors.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.High-resolution analysis of copy number alterations and associated expression changes in ovarian tumors.CGHregions: dimension reduction for array CGH data with minimal information lossModel-based clustering of array CGH data.CMDS: a population-based method for identifying recurrent DNA copy number aberrations in cancer from high-resolution data.An ANOCEF genomic and transcriptomic microarray study of the response to radiotherapy or to alkylating first-line chemotherapy in glioblastoma patients.Discovering tumor suppressor genes through genome-wide copy number analysis.Identification of differential aberrations in multiple-sample array CGH studiesGenetic characterization of large parathyroid adenomasGenomic landscape of pancreatic neuroendocrine tumorsCancer gene discovery in mouse and man.CAPweb: a bioinformatics CGH array Analysis PlatformGSTT1 copy number gain and ZNF overexpression are predictors of poor response to imatinib in gastrointestinal stromal tumorsCopy number alterations in small intestinal neuroendocrine tumors determined by array comparative genomic hybridizationStability-based comparison of class discovery methods for DNA copy number profiles.Genome-wide scan identifies a copy number variable region at 3p21.1 that influences the TLR9 expression levels in IgA nephropathy patientsDetecting simultaneous changepoints in multiple sequences.High-resolution aCGH and expression profiling identifies a novel genomic subtype of ER negative breast cancerCombining chromosomal arm status and significantly aberrant genomic locations reveals new cancer subtypesSequential model selection-based segmentation to detect DNA copy number variation.RJaCGH: Bayesian analysis of aCGH arrays for detecting copy number changes and recurrent regions.Improved Statistical Analysis for Array CGH-Based DNA Copy Number Aberrations.A scale-space method for detecting recurrent DNA copy number changes with analytical false discovery rate control.A Novel Graph-based Algorithm to Infer Recurrent Copy Number Variations in Cancer.Prevalence of targetable oncogenic mutations and genomic alterations in Epstein-Barr virus-associated diffuse large B-cell lymphoma of the elderly.Joint segmentation, calling, and normalization of multiple CGH profiles.A Bayesian segmentation approach to ascertain copy number variations at the population level.Array CGH demonstrates characteristic aberration signatures in human papillary thyroid carcinomas governed by RET/PTC.DNA copy number alterations, gene expression changes and disease-free survival in patients with colorectal cancer: a 10 year follow-up.Array CGH and gene-expression profiling reveals distinct genomic instability patterns associated with DNA repair and cell-cycle checkpoint pathways in Ewing's sarcoma.Comparison of Clinical Subgroup aCGH Profiles through Pseudolikelihood Ratio Tests.
P2860
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P2860
Computation of recurrent minimal genomic alterations from array-CGH data.
description
2006 nî lūn-bûn
@nan
2006 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հունվարին 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
Computation of recurrent minimal genomic alterations from array-CGH data.
@ast
Computation of recurrent minimal genomic alterations from array-CGH data.
@en
type
label
Computation of recurrent minimal genomic alterations from array-CGH data.
@ast
Computation of recurrent minimal genomic alterations from array-CGH data.
@en
prefLabel
Computation of recurrent minimal genomic alterations from array-CGH data.
@ast
Computation of recurrent minimal genomic alterations from array-CGH data.
@en
P2093
P356
P1433
P1476
Computation of recurrent minimal genomic alterations from array-CGH data.
@en
P2093
P304
P356
10.1093/BIOINFORMATICS/BTL004
P407
P577
2006-01-24T00:00:00Z