VAMP: Visualization and analysis of array-CGH, transcriptome and other molecular profiles
暂无分享,去创建一个
Céline Rouveirol | Emmanuel Barillot | Nicolas Servant | Isabelle Janoueix-Lerosey | Philippe Hupé | Philippe La Rosa | Olivier Delattre | Pierre Neuvial | Isabel Brito | Stéphane Liva | Elodie Manié | Caroline Brennetot | Eric Viara | Nicolas Robine | Séverine Lair | Nicolas Stransky | Gaëlle Pierron | Virginie Raynal | Nadège Gruel | Marc-Henri Stern | Alain Aurias | François Radvanyi | Nicolas Stransky | P. Neuvial | E. Barillot | C. Rouveirol | O. Delattre | F. Radvanyi | N. Robine | A. Aurias | M. Stern | N. Servant | P. Hupé | E. Viara | I. Janoueix-Lerosey | G. Pierron | P. L. Rosa | S. Liva | S. Lair | Caroline Brennetot | N. Gruel | Elodie Manié | V. Raynal | I. Brito | N. Stransky
[1] Christian A. Rees,et al. Microarray analysis reveals a major direct role of DNA copy number alteration in the transcriptional program of human breast tumors , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[2] Emmanuel Barillot,et al. Analysis of array CGH data: from signal ratio to gain and loss of DNA regions , 2004, Bioinform..
[3] Calum MacAulay,et al. SeeGH – A software tool for visualization of whole genome array comparative genomic hybridization data , 2004, BMC Bioinformatics.
[4] N. Carter,et al. Array Comparative Genomic Hybridization Analysis of Colorectal Cancer Cell Lines and Primary Carcinomas , 2004, Cancer Research.
[5] M. Wigler,et al. Circular binary segmentation for the analysis of array-based DNA copy number data. , 2004, Biostatistics.
[6] H. Döhner,et al. Matrix‐based comparative genomic hybridization: Biochips to screen for genomic imbalances , 1997, Genes, chromosomes & cancer.
[7] Jane Fridlyand,et al. High-resolution analysis of DNA copy number alterations in colorectal cancer by array-based comparative genomic hybridization. , 2004, Carcinogenesis.
[8] Y. Nakamura,et al. Allelotype of colorectal carcinomas. , 1989, Science.
[9] M. Shapero,et al. High-resolution analysis of DNA copy number using oligonucleotide microarrays. , 2004, Genome research.
[10] W. Kuo,et al. High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays , 1998, Nature Genetics.
[11] Elena Marchiori,et al. Chromosomal Breakpoint Detection in Human Cancer , 2003, EvoWorkshops.
[12] Ali S. Hadi,et al. Finding Groups in Data: An Introduction to Chster Analysis , 1991 .
[13] Franck Picard,et al. A statistical approach for array CGH data analysis , 2005, BMC Bioinformatics.
[14] Wei Chen,et al. CGHPRO – A comprehensive data analysis tool for array CGH , 2005, BMC Bioinformatics.
[15] D. Albertson,et al. Chromosome aberrations in solid tumors , 2003, Nature Genetics.
[16] Emmanuel Barillot,et al. Spatial normalization of array-CGH data , 2006, BMC Bioinformatics.
[17] Céline Rouveirol,et al. Bioinformatics Original Paper Computation of Recurrent Minimal Genomic Alterations from Array-cgh Data , 2022 .
[18] Peter J. Rousseeuw,et al. Finding Groups in Data: An Introduction to Cluster Analysis , 1990 .
[19] L. Recht,et al. High-resolution genome-wide mapping of genetic alterations in human glial brain tumors. , 2005, Cancer research.
[20] Tom H. Pringle,et al. The human genome browser at UCSC. , 2002, Genome research.
[21] Emmanuel Barillot,et al. Preferential Occurrence of Chromosome Breakpoints within Early Replicating Regions in Neuroblastoma , 2005, Cell cycle.
[22] John Quackenbush,et al. CGHAnalyzer: a stand-alone software package for cancer genome analysis using array-based DNA copy number data , 2005, Bioinform..
[23] J. Lieb,et al. ChIP-chip: considerations for the design, analysis, and application of genome-wide chromatin immunoprecipitation experiments. , 2004, Genomics.
[24] Rui Li,et al. Array-based comparative genomic hybridization reveals recurrent chromosomal aberrations and Jab1 as a potential target for 8q gain in hepatocellular carcinoma. , 2005, Carcinogenesis.
[25] Keith W. Jones,et al. Whole genome DNA copy number changes identified by high density oligonucleotide arrays , 2004, Human Genomics.
[26] Paul H. C. Eilers,et al. Quantile smoothing of array CGH data , 2005, Bioinform..
[27] J. Fridlyand,et al. Rare amplicons implicate frequent deregulation of cell fate specification pathways in oral squamous cell carcinoma , 2005, Oncogene.
[28] Ajay N. Jain,et al. Assembly of microarrays for genome-wide measurement of DNA copy number , 2001, Nature Genetics.
[29] M. McMahon,et al. Analysis of genomic DNA alterations and mRNA expression patterns in a panel of human pancreatic cancer cell lines , 2005, Genes, chromosomes & cancer.
[30] Eugene Berezikov,et al. CONREAL web server: identification and visualization of conserved transcription factor binding sites , 2005, Nucleic Acids Res..
[31] Randy D Gascoyne,et al. Comprehensive whole genome array CGH profiling of mantle cell lymphoma model genomes. , 2004, Human molecular genetics.
[32] Jaime Prilusky,et al. SPACE: a suite of tools for protein structure prediction and analysis based on complementarity and environment , 2005, Nucleic Acids Res..
[33] Qing-Rong Chen,et al. Detection of low level genomic alterations by comparative genomic hybridization based on cDNA micro-arrays , 2005, Bioinform..
[34] J. Schimenti,et al. Synapsis or silence , 2005, Nature Genetics.
[35] Ajay N. Jain,et al. Hidden Markov models approach to the analysis of array CGH data , 2004 .
[36] D. Pinkel,et al. Array comparative genomic hybridization and its applications in cancer , 2005, Nature Genetics.
[37] Bradley P. Coe,et al. A tiling resolution DNA microarray with complete coverage of the human genome , 2004, Nature Genetics.
[38] Wen-Lin Kuo,et al. Array-based comparative genomic hybridization for genome-wide screening of DNA copy number in bladder tumors. , 2003, Cancer research.