Breakpoint identification and smoothing of array comparative genomic hybridization data.
about
SW-ARRAY: a dynamic programming solution for the identification of copy-number changes in genomic DNA using array comparative genome hybridization dataRapid detection of genomic imbalances using micro-arrays consisting of pooled BACs covering all human chromosome arms.Human and mouse oligonucleotide-based array CGH.arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays.Large fragment Bst DNA polymerase for whole genome amplification of DNA from formalin-fixed paraffin-embedded tissuesDivergent genomic and epigenomic landscapes of lung cancer subtypes underscore the selection of different oncogenic pathways during tumor developmentParsimonious higher-order hidden Markov models for improved array-CGH analysis with applications to Arabidopsis thaliana.Genomic markers for malignant progression in pulmonary adenocarcinoma with bronchioloalveolar featuresComparative analysis of algorithms for identifying amplifications and deletions in array CGH data.CGHScan: finding variable regions using high-density microarray comparative genomic hybridization data.Exploiting noise in array CGH data to improve detection of DNA copy number change.aCGHViewer: a generic visualization tool for aCGH data.Normalization of array-CGH data: influence of copy number imbalances.MD-SeeGH: a platform for integrative analysis of multi-dimensional genomic data.GeneCount: genome-wide calculation of absolute tumor DNA copy numbers from array comparative genomic hybridization data.Quantile smoothing of array CGH data.Genomic alterations identified by array comparative genomic hybridization as prognostic markers in tamoxifen-treated estrogen receptor-positive breast cancer.SIGMA: a system for integrative genomic microarray analysis of cancer genomes.High-resolution copy number analysis of paraffin-embedded archival tissue using SNP BeadArrays.A forward-backward fragment assembling algorithm for the identification of genomic amplification and deletion breakpoints using high-density single nucleotide polymorphism (SNP) array.Using expression arrays for copy number detection: an example from E. coliAnalysis of array CGH data for cancer studies using fused quantile regression.DNA copy number profiles of gastric cancer precursor lesions.SIRAC: Supervised Identification of Regions of Aberration in aCGH datasets.Jacobsen syndrome and Beckwith-Wiedemann syndrome caused by a parental pericentric inversion inv(11)(p15q24).Array CGH data modeling and smoothing in Stationary Wavelet Packet Transform domain.Advanced analysis and visualization of gene copy number and expression dataAlterations in genes of the EGFR signaling pathway and their relationship to EGFR tyrosine kinase inhibitor sensitivity in lung cancer cell lines.Comparative genomic hybridization: microarray design and data interpretation.Overlay tool for aCGHViewer: an analysis module built for aCGHViewer used to perform comparisons of data derived from different microarray platforms.Normalized, segmented or called aCGH data?Genomic profiling distinguishes familial multiple and sporadic multiple meningiomas.Gene copy number analysis for family data using semiparametric copula model.Anti-proliferative action of vitamin D in MCF7 is still active after siRNA-VDR knock-downCGI: Java software for mapping and visualizing data from array-based comparative genomic hybridization and expression profilingCMDS: a population-based method for identifying recurrent DNA copy number aberrations in cancer from high-resolution data.Transcriptome profiles of carcinoma-in-situ and invasive non-small cell lung cancer as revealed by SAGEAn integrative multi-dimensional genetic and epigenetic strategy to identify aberrant genes and pathways in cancer.Integrative genomic analyses identify BRF2 as a novel lineage-specific oncogene in lung squamous cell carcinomaA genome assembly-integrated dog 1 Mb BAC microarray: a cytogenetic resource for canine cancer studies and comparative genomic analysis.
P2860
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P2860
Breakpoint identification and smoothing of array comparative genomic hybridization data.
description
2004 nî lūn-bûn
@nan
2004 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի հունիսին 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
Breakpoint identification and smoothing of array comparative genomic hybridization data.
@ast
Breakpoint identification and smoothing of array comparative genomic hybridization data.
@en
type
label
Breakpoint identification and smoothing of array comparative genomic hybridization data.
@ast
Breakpoint identification and smoothing of array comparative genomic hybridization data.
@en
prefLabel
Breakpoint identification and smoothing of array comparative genomic hybridization data.
@ast
Breakpoint identification and smoothing of array comparative genomic hybridization data.
@en
P2093
P356
P1433
P1476
Breakpoint identification and smoothing of array comparative genomic hybridization data.
@en
P2093
A V D Vaart
Elena Marchiori
Gerrit Meijer
P304
P356
10.1093/BIOINFORMATICS/BTH355
P407
P50
P577
2004-06-16T00:00:00Z