CiteULike: Zephyrus's Hurles:ME [4 articles]

Origins and functional impact of copy number variation in the human genome

Nature In Nature, Vol. advance online publication (07 October 2009)

posted to review impact genome cnv by Zephyrus on 2009-11-20 05:48:37 as

along with 21 people and 1 group n00c gthorisson vplagnol biovils psique chvlyl daed daforerog zufar jessopher DrRichardBadge operon colinveal frohike sf11 sameersoi polivares dswan qayub bpcusack rdiaz Journal picks

Relative impact of nucleotide and copy number variation on gene expression phenotypes.

Science (New York, N.Y.), Vol. 315, No. 5813. (9 February 2007), pp. 848-853.

by Barbara E. Stranger, Matthew S. Forrest, Mark Dunning, et al.Catherine E. Ingle, Claude Beazley, Natalie Thorne, Richard Redon, Christine P. Bird, Anna de Grassi, Charles Lee, Chris Tyler-Smith, Nigel Carter, Stephen W. Scherer, Simon Tavaré, Panagiotis Deloukas, Matthew E. Hurles, Emmanouil T. Dermitzakis

Paired-End Mapping Reveals Extensive Structural Variation in the Human Genome

Science In Science, Vol. 318, No. 5849. (19 October 2007), pp. 420-426.

A robust statistical method for case-control association testing with copy number variation.

Nature genetics, Vol. 40, No. 10. (7 October 2008), pp. 1245-1252.

by Chris Barnes, Vincent Plagnol, Tomas Fitzgerald, et al.Richard Redon, Jonathan Marchini, David Clayton, Matthew E. Hurles

posted to association cancer-crosstalk case-control cnv statistics by Zephyrus on 2008-10-04 08:44:36 as

along with 16 people and 1 group biovils daed zufar daforerog pengchy ptrobajo vplagnol waszak caseybrown dakelley buyske misonneh djkt rdiaz Stew guhjy Roswell Cancer Crosstalk

	Origins and functional impact of copy number variation in the human genome [My Copy] Nature In Nature, Vol. advance online publication (07 October 2009) by Donald F. Conrad, Dalila Pinto, Richard Redon, et al.Lars Feuk, Omer Gokcumen, Yujun Zhang, Jan Aerts, T. Daniel Andrews, Chris Barnes, Peter Campbell, Tomas Fitzgerald, Min Hu, Chun H. Ihm, Kati Kristiansson, Daniel G. MacArthur, Jeffrey R. MacDonald, Ifejinelo Onyiah, Andy W. Pang, Sam Robson, Kathy Stirrups, Armand Valsesia, Klaudia Walter, John Wei, Chris Tyler-Smith, Nigel P. Carter, Charles Lee, Stephen W. Scherer, Matthew E. Hurles posted to review impact genome cnv by Zephyrus on 2009-11-20 05:48:37 as along with 21 people and 1 group n00c gthorisson vplagnol biovils psique chvlyl daed daforerog zufar jessopher DrRichardBadge operon colinveal frohike sf11 sameersoi polivares dswan qayub bpcusack rdiaz Journal picks
	Relative impact of nucleotide and copy number variation on gene expression phenotypes. [My Copy] Science (New York, N.Y.), Vol. 315, No. 5813. (9 February 2007), pp. 848-853. by Barbara E. Stranger, Matthew S. Forrest, Mark Dunning, et al.Catherine E. Ingle, Claude Beazley, Natalie Thorne, Richard Redon, Christine P. Bird, Anna de Grassi, Charles Lee, Chris Tyler-Smith, Nigel Carter, Stephen W. Scherer, Simon Tavaré, Panagiotis Deloukas, Matthew E. Hurles, Emmanouil T. Dermitzakis posted to variaton snp primer phenotype impact genetics cnv by Zephyrus on 2009-09-15 21:04:11 as along with 32 people and 5 groups biovils lp2 daveGerrard sameersoi timhubbard ajbattle jonilaserson ilyashl emptyhb buyske zufar koller waszak daed psique jo_davies srp33 guhjy jfr dpollard balicea rdiaz qfwills djkt vplagnol shigepong jlangdon xingxu cisevol caseybrown frohike jandot Roswell Cancer Crosstalk Visiting Position Bioinformatics EisenLab cis-regulatory-evolution
	Paired-End Mapping Reveals Extensive Structural Variation in the Human Genome [My Copy] Science In Science, Vol. 318, No. 5849. (19 October 2007), pp. 420-426. by Jan O. Korbel, Alexander E. Urban, Jason P. Affourtit, et al.Brian Godwin, Fabian Grubert, Jan F. Simons, Philip M. Kim, Dean Palejev, Nicholas J. Carriero, Lei Du, Bruce E. Taillon, Zhoutao Chen, Andrea Tanzer, A. C. Eugenia Saunders, Jianxiang Chi, Fengtang Yang, Nigel P. Carter, Matthew E. Hurles, Sherman M. Weissman, Timothy T. Harkins, Mark B. Gerstein, Michael Egholm, Michael Snyder posted to detection epidemiology genetic genome structural variation by Zephyrus on 2009-02-22 13:20:19 as along with 22 people and 2 groups torfinnnome jandot n00c jonilaserson jrvalcourt APRegier jessopher hpaces pkonings orzenil stuetz matthewsuderman dpollard dchughes AaronDarling rdiaz giovanni jlangdon annacarina07 Neeperando jfr caseybrown Journal picks EisenLab
	A robust statistical method for case-control association testing with copy number variation. [My Copy] Nature genetics, Vol. 40, No. 10. (7 October 2008), pp. 1245-1252. by Chris Barnes, Vincent Plagnol, Tomas Fitzgerald, et al.Richard Redon, Jonathan Marchini, David Clayton, Matthew E. Hurles posted to association cancer-crosstalk case-control cnv statistics by Zephyrus on 2008-10-04 08:44:36 as along with 16 people and 1 group biovils daed zufar daforerog pengchy ptrobajo vplagnol waszak caseybrown dakelley buyske misonneh djkt rdiaz Stew guhjy Roswell Cancer Crosstalk

Zephyrus's Hurles:ME [4 articles] Export

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