Circular binary segmentation for the analysis of array-based DNA copy number data
about
Tensor GSVD of patient- and platform-matched tumor and normal DNA copy-number profiles uncovers chromosome arm-wide patterns of tumor-exclusive platform-consistent alterations encoding for cell transformation and predicting ovarian cancer survivalGSVD comparison of patient-matched normal and tumor aCGH profiles reveals global copy-number alterations predicting glioblastoma multiforme survivalBAIT: Organizing genomes and mapping rearrangements in single cellsLarge-scale data integration framework provides a comprehensive view on glioblastoma multiformeGenomic and epigenetic evidence for oxytocin receptor deficiency in autismComputational tools for copy number variation (CNV) detection using next-generation sequencing data: features and perspectivesDNA methylation changes in genes frequently mutated in sporadic colorectal cancer and in the DNA repair and Wnt/β-catenin signaling pathway genesA complex genomic rearrangement involving the endothelin 3 locus causes dermal hyperpigmentation in the chickenCovariate assisted screening and estimationHuman CLP1 mutations alter tRNA biogenesis, affecting both peripheral and central nervous system functionEGFR/Met association regulates EGFR TKI resistance in breast cancermicroRNAs exhibit high frequency genomic alterations in human cancerGenomic 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 tumorsPrognostic significance of copy-number alterations in multiple myelomaMET amplification occurs with or without T790M mutations in EGFR mutant lung tumors with acquired resistance to gefitinib or erlotinibIntegrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1Molecular inversion probes reveal patterns of 9p21 deletion and copy number aberrations in childhood leukemiaA statistical approach for array CGH data analysisSW-ARRAY: a dynamic programming solution for the identification of copy-number changes in genomic DNA using array comparative genome hybridization dataAllele-specific amplification in cancer revealed by SNP array analysisCGHPRO -- a comprehensive data analysis tool for array CGH.CARAT: a novel method for allelic detection of DNA copy number changes using high density oligonucleotide arrays.Computational methods for detecting copy number variations in cancer genome using next generation sequencing: principles and challengesStructural variation discovery in the cancer genome using next generation sequencing: computational solutions and perspectivesModified screening and ranking algorithm for copy number variation detection.A high-resolution map of segmental DNA copy number variation in the mouse genomeElusive copy number variation in the mouse genomeCharacterization of a novel radiation-induced sarcoma cell lineMutational Landscapes of Sequential Prostate Metastases and Matched Patient Derived Xenografts during Enzalutamide TherapyWhole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine.Integrative clinical genomics of advanced prostate cancer.Focal DNA copy number changes in neuroblastoma target MYCN regulated genesVariation in crossover frequencies perturb crossover assurance without affecting meiotic chromosome segregation in Saccharomyces cerevisiaeGenome-wide copy number profiling on high-density bacterial artificial chromosomes, single-nucleotide polymorphisms, and oligonucleotide microarrays: a platform comparison based on statistical power analysisDetectable clonal mosaicism from birth to old age and its relationship to cancerAssessment of megabase-scale somatic copy number variation using single-cell sequencingConfirmation of the reported association of clonal chromosomal mosaicism with an increased risk of incident hematologic cancerA genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin doseFenton reaction induced cancer in wild type rats recapitulates genomic alterations observed in human cancerAnalysis of molecular cytogenetic alteration in rhabdomyosarcoma by array comparative genomic hybridization
P2860
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P2860
Circular binary segmentation for the analysis of array-based DNA copy number data
description
2004 nî lūn-bûn
@nan
2004 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
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
name
Circular binary segmentation for the analysis of array-based DNA copy number data
@ast
Circular binary segmentation for the analysis of array-based DNA copy number data
@en
type
label
Circular binary segmentation for the analysis of array-based DNA copy number data
@ast
Circular binary segmentation for the analysis of array-based DNA copy number data
@en
prefLabel
Circular binary segmentation for the analysis of array-based DNA copy number data
@ast
Circular binary segmentation for the analysis of array-based DNA copy number data
@en
P2093
P3181
P356
P1433
P1476
Circular binary segmentation for the analysis of array-based DNA copy number data
@en
P2093
Adam B Olshen
E S Venkatraman
Robert Lucito
P304
P3181
P356
10.1093/BIOSTATISTICS/KXH008
P407
P577
2004-10-01T00:00:00Z