SW-ARRAY: a dynamic programming solution for the identification of copy-number changes in genomic DNA using array comparative genome hybridization data
about
Elusive copy number variation in the mouse genomeSnoopCGH: software for visualizing comparative genomic hybridization dataFast Bayesian Inference of Copy Number Variants using Hidden Markov Models with Wavelet CompressionAsterias: a parallelized web-based suite for the analysis of expression and aCGH dataParsimonious higher-order hidden Markov models for improved array-CGH analysis with applications to Arabidopsis thaliana.Flexible and accurate detection of genomic copy-number changes from aCGH.FISH Oracle: a web server for flexible visualization of DNA copy number data in a genomic context.Interpreting genomic data via entropic dissection.Genovar: a detection and visualization tool for genomic variants.Asterias: integrated analysis of expression and aCGH data using an open-source, web-based, parallelized software suite.ADaCGH: A parallelized web-based application and R package for the analysis of aCGH data.A forward-backward fragment assembling algorithm for the identification of genomic amplification and deletion breakpoints using high-density single nucleotide polymorphism (SNP) array.Improved detection of global copy number variation using high density, non-polymorphic oligonucleotide probesCharacterization of hemizygous deletions in citrus using array-comparative genomic hybridization and microsynteny comparisons with the poplar genomeComparative genomic hybridization: microarray design and data interpretation.CGHnormaliter: an iterative strategy to enhance normalization of array CGH data with imbalanced aberrationsDynamic and physical clustering of gene expression during epidermal barrier formation in differentiating keratinocytesCGI: Java software for mapping and visualizing data from array-based comparative genomic hybridization and expression profilingConditional random pattern model for copy number aberration detection.Population-genetic nature of copy number variations in the human genome.rSW-seq: algorithm for detection of copy number alterations in deep sequencing data.Copy number variations in East-Asian population and their evolutionary and functional implicationsOn the adaptive partition approach to the detection of multiple change-points.Genomic imbalances are confined to non-proliferating cells in paediatric patients with acute myeloid leukaemia and a normal or incomplete karyotype.A multi-sample based method for identifying common CNVs in normal human genomic structure using high-resolution aCGH dataDiscovering tumor suppressor genes through genome-wide copy number analysis.An all-statistics, high-speed algorithm for the analysis of copy number variation in genomesAccurate and reliable high-throughput detection of copy number variation in the human genome.Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays.Genome instability model of metastatic neuroblastoma tumorigenesis by a dictionary learning algorithm.Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia.CNVs into the wild: screening the genomes of conifer trees (Picea spp.) reveals fewer gene copy number variations in hybrids and links to adaptation.Identification of disease genes by whole genome CGH arrays.α-Thalassemia, mental retardation, and myelodysplastic syndrome.Methods and strategies for analyzing copy number variation using DNA microarrays.A novel framework for the identification and analysis of duplicons between human and chimpanzee.Sites of differential DNA methylation between placenta and peripheral blood: molecular markers for noninvasive prenatal diagnosis of aneuploidies.The Role of Constitutional Copy Number Variants in Breast Cancer.A comprehensive profile of DNA copy number variations in a Korean population: identification of copy number invariant regions among KoreansA new method for non-invasive prenatal diagnosis of Down syndrome using MeDIP real time qPCR.
P2860
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P2860
SW-ARRAY: a dynamic programming solution for the identification of copy-number changes in genomic DNA using array comparative genome hybridization data
description
2005 nî lūn-bûn
@nan
2005 թուականին հրատարակուած գիտական յօդուած
@hyw
2005 թվականին 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
SW-ARRAY: a dynamic programmin ...... tive genome hybridization data
@ast
SW-ARRAY: a dynamic programmin ...... tive genome hybridization data
@en
SW-ARRAY: a dynamic programmin ...... tive genome hybridization data
@nl
type
label
SW-ARRAY: a dynamic programmin ...... tive genome hybridization data
@ast
SW-ARRAY: a dynamic programmin ...... tive genome hybridization data
@en
SW-ARRAY: a dynamic programmin ...... tive genome hybridization data
@nl
prefLabel
SW-ARRAY: a dynamic programmin ...... tive genome hybridization data
@ast
SW-ARRAY: a dynamic programmin ...... tive genome hybridization data
@en
SW-ARRAY: a dynamic programmin ...... tive genome hybridization data
@nl
P2093
P2860
P50
P3181
P356
P1476
SW-ARRAY: a dynamic programmin ...... tive genome hybridization data
@en
P2093
Ana Tiganescu
Andy Greenfield
Anita Salhan
Asa Hedman
Douglas R Higgs
Helena Ayyub
John Broxholme
Nicki Ventress
P2860
P304
P3181
P356
10.1093/NAR/GKI643
P407
P577
2005-01-01T00:00:00Z