bib copy number variations (2003)

Bibliography on copy number variations (2003)

front page
2008
2007
2006
2005
2004
2003
2002
2001
2000
90s
glossary
links
programs

Christopher I Amosa, Sanjay Shetea, Jianfang Chena, Robert K Yu (2003), "Positional identification of microdeletions with genetic markers", Human Heredity, 56:107-118.
Reija Autio, Sampsa Hautaniemi, Päivikki Kauraniemi, Olli Yli-Harja, Jaakko Astola, Maija Wolf, Anne Kallioniemi (2003), "CGH-Plotter: MATLAB toolbox for CGH-data analysis", Bioinformatics, 19(13):1714-1715.
[abstract]
K Jong, E Marchiori, A Vaart, B Ylstra, M Weiss, G Meijer (2003), "Chromosomal breakpoint detection in human cancer", in Evolutionary Computing: Evolutionary Computation and Bioinformatics, Vol 2611, pp.54-56 (Springer).
Devin P Locke, Richard Segraves, Lucia Carbone, Nicoletta Archidiacono, Donna G Albertson, Daniel Pinkel, Evan E Eichler (2003), "Large-scale variation among human and Great Ape genomes determined by array comparative genomic hybridization", Genome Research, 13(3):347-357.
[abstract]
R Lucito, J Healy, J Alexander, A Reiner, D Esposito, M Chi, L Rodgers, A Brady, J Sebat, J Troge, JA West, S Rostan, KC Nguyen, S Powers, KQ Ye, A Olshen, E Venkatraman, L Norton, M Wigler (2003), "Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation", Genome Research, 13(10):2291-2305.
[abstract]
Joris A Veltman, Jane Fridlyand, Sunanda Pejavar, Adam B Olshen, James E Korkola, Sandy DeVries, Peter Carroll, Wen-Lin Kuo, Daniel Pinkel, Donna Albertson, Carlos Cordon-Cardo, Ajay N Jain, Frederic M Waldman (2003), "Array-based comparative genomic hybridization for genome-wide screening of DNA copy number in bladder tumors", Cancer Research, 63:2872-2880.
[abstract]

		Bibliography on copy number variations (2003)
	front page 2008 2007 2006 2005 2004 2003 2002 2001 2000 90s glossary links programs	Christopher I Amosa, Sanjay Shetea, Jianfang Chena, Robert K Yu (2003), "Positional identification of microdeletions with genetic markers", Human Heredity, 56:107-118. Reija Autio, Sampsa Hautaniemi, Päivikki Kauraniemi, Olli Yli-Harja, Jaakko Astola, Maija Wolf, Anne Kallioniemi (2003), "CGH-Plotter: MATLAB toolbox for CGH-data analysis", Bioinformatics, 19(13):1714-1715. [abstract] K Jong, E Marchiori, A Vaart, B Ylstra, M Weiss, G Meijer (2003), "Chromosomal breakpoint detection in human cancer", in Evolutionary Computing: Evolutionary Computation and Bioinformatics, Vol 2611, pp.54-56 (Springer). Devin P Locke, Richard Segraves, Lucia Carbone, Nicoletta Archidiacono, Donna G Albertson, Daniel Pinkel, Evan E Eichler (2003), "Large-scale variation among human and Great Ape genomes determined by array comparative genomic hybridization", Genome Research, 13(3):347-357. [abstract] R Lucito, J Healy, J Alexander, A Reiner, D Esposito, M Chi, L Rodgers, A Brady, J Sebat, J Troge, JA West, S Rostan, KC Nguyen, S Powers, KQ Ye, A Olshen, E Venkatraman, L Norton, M Wigler (2003), "Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation", Genome Research, 13(10):2291-2305. [abstract] Joris A Veltman, Jane Fridlyand, Sunanda Pejavar, Adam B Olshen, James E Korkola, Sandy DeVries, Peter Carroll, Wen-Lin Kuo, Daniel Pinkel, Donna Albertson, Carlos Cordon-Cardo, Ajay N Jain, Frederic M Waldman (2003), "Array-based comparative genomic hybridization for genome-wide screening of DNA copy number in bladder tumors", Cancer Research, 63:2872-2880. [abstract]