frohike's Lee:C [12 articles] Export Sort

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	Exome sequencing identifies the cause of a mendelian disorder [My Copy] Nature Genetics In Nat Genet, Vol. 42, No. 1. (13 November 2009), pp. 30-35. by Sarah B. Ng, Kati J. Buckingham, Choli Lee, et al.Abigail W. Bigham, Holly K. Tabor, Karin M. Dent, Chad D. Huff, Paul T. Shannon, Ethylin W. Jabs, Deborah A. Nickerson, Jay Shendure, Michael J. Bamshad posted to sequencing exome by frohike on 2009-12-29 11:56:23 as along with 7 people n00c cajunsushi pst seb1 daforerog Peiyong psique
	A small-cell lung cancer genome with complex signatures of tobacco exposure [My Copy] Nature, Vol. advance online publication (16 December 2009) by Erin D. Pleasance, Philip J. Stephens, Sarah OâMeara, et al.David J. McBride, Alison Meynert, David Jones, Meng-Lay Lin, David Beare, King W. Lau, Chris Greenman, Ignacio Varela, Serena Nik-Zainal, Helen R. Davies, Gonzalo R. OrdoÃ±ez, Laura J. Mudie, Calli Latimer, Sarah Edkins, Lucy Stebbings, Lina Chen, Mingming Jia, Catherine Leroy, John Marshall, Andrew Menzies, Adam Butler, Jon W. Teague, Jonathon Mangion, Yongming A. Sun, Stephen F. McLaughlin, Heather E. Peckham, Eric F. Tsung, Gina L. Costa, Clarence C. Lee, John D. Minna, Adi Gazdar, Ewan Birney, Michael D. Rhodes, Kevin J. McKernan, Michael R. Stratton, P. Andrew Futreal, Peter J. Campbell posted to tobacco_exposure mutation lung-cancer by frohike on 2009-12-17 12:29:18 as along with 3 people ealloza pavanghatty neils
	The fine-scale and complex architecture of human copy-number variation. [My Copy] American journal of human genetics, Vol. 82, No. 3. (24 March 2008), pp. 685-695. by George H. Perry, Amir Ben-Dor, Anya Tsalenko, et al.Nick Sampas, Laia Rodriguez-Revenga, Charles W. Tran, Alicia Scheffer, Israel Steinfeld, Peter Tsang, N. Alice Yamada, Han Soo S. Park, Jong-Il I. Kim, Jeong-Sun S. Seo, Zohar Yakhini, Stephen Laderman, Laurakay Bruhn, Charles Lee posted to hapmap cnv cgh by frohike on 2009-12-16 10:27:31 as along with 5 people psique daforerog vplagnol daed guhjy
	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 tiling-array normal human-genome database-genomic-variants cnv 1kb-cnv by frohike on 2009-10-14 12:14:11 as along with 21 people and 1 group n00c Zephyrus gthorisson vplagnol biovils psique chvlyl daed daforerog zufar jessopher DrRichardBadge operon colinveal sf11 sameersoi polivares dswan qayub bpcusack rdiaz Journal picks
	Targeted capture and massively parallel sequencing of 12 human exomes. [My Copy] Nature, Vol. 461, No. 7261. (10 September 2009), pp. 272-276. by Sarah B. Ng, Emily H. Turner, Peggy D. Robertson, et al.Steven D. Flygare, Abigail W. Bigham, Choli Lee, Tristan Shaffer, Michelle Wong, Arindam Bhattacharjee, Evan E. Eichler, Michael Bamshad, Deborah A. Nickerson, Jay Shendure posted to second-generation-sequencing sequencing human exome by frohike on 2009-08-16 21:28:43 as along with 23 people and 1 group seb1 hzoltan liqbbi chvlyl ongenetics psique fenghezi n00c dswan jmanning2k torfinnnome GeeSharpMinor pkonings neils djkt daforerog PabloMarin stubrown danmaclean xingxu vplagnol druvus jandot Journal picks
	Structural variation in the human genome: the impact of copy number variants on clinical diagnosis. [My Copy] Genetics in medicine : official journal of the American College of Medical Genetics, Vol. 9, No. 9. (September 2007), pp. 600-606. by L. Rodriguez-Revenga, M. Mila, C. Rosenberg, A. Lamb, C. Lee posted to arraycgh benign cnv human malignant by frohike on 2008-11-04 11:10:34 as along with 3 people and 1 group brianb misonneh Zephyrus Roswell Cancer Crosstalk
	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 gene-expression cnv microarray phenotype snp by frohike on 2008-08-08 10:32:17 as along with 32 people and 5 groups biovils lp2 daveGerrard sameersoi timhubbard Zephyrus 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 jandot Roswell Cancer Crosstalk Visiting Position Bioinformatics EisenLab cis-regulatory-evolution
	Global variation in copy number in the human genome [My Copy] Nature In Nature, Vol. 444, No. 7118. (23 November 2006), pp. 444-454. by Richard Redon, Shumpei Ishikawa, Karen R. Fitch, et al.Lars Feuk, George H. Perry, T. Daniel Andrews, Heike Fiegler, Michael H. Shapero, Andrew R. Carson, Wenwei Chen, Eun K. Cho, Stephanie Dallaire, Jennifer L. Freeman, Juan R. Gonzalez, Monica Gratacos, Jing Huang, Dimitrios Kalaitzopoulos, Daisuke Komura, Jeffrey R. MacDonald, Christian R. Marshall, Rui Mei, Lyndal Montgomery, Kunihiro Nishimura, Kohji Okamura, Fan Shen, Martin J. Somerville, Joelle Tchinda, Armand Valsesia, Cara Woodwark, Fengtang Yang, Junjun Zhang, Tatiana Zerjal, Jane Zhang, Lluis Armengol, Donald F. Conrad, Xavier Estivill, Chris Tyler-Smith, Nigel P. Carter, Hiroyuki Aburatani, Charles Lee, Keith W. Jones, Stephen W. Scherer, Matthew E. Hurles posted to snp human genomics cnv by frohike on 2007-01-12 11:27:09 as along with 44 people and 7 groups shigepong shikin n00c sameersoi lp2 ilyashl ajbattle darian jonilaserson jrvalcourt turnersd guhjy daforerog noushin Glires ivanek waszak jo_davies psique bpb jfr balajis pradiptaray dpollard mtagaya adepace aswin rdiaz qfwills ealloza vplagnol giovanni jeremymiller vpschulz raiyar ramensky ccr azazello dbgrant colinveal xingxu srp33 Ema daed parkinson's disease references Bioinformatics EisenLab BioinfoCIPF GeschwindLab steinmetzlab MBLAB
	Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays. [My Copy] Genome research, Vol. 16, No. 12. (1 December 2006), pp. 1575-1584. by Daisuke Komura, Fan Shen, Shumpei Ishikawa, et al.Karen R. Fitch, Wenwei Chen, Jane Zhang, Guoying Liu, Sigeo Ihara, Hiroshi Nakamura, Matthew E. Hurles, Charles Lee, Stephen W. Scherer, Keith W. Jones, Michael H. Shapero, Jing Huang, Hiroyuki Aburatani posted to snp human cnv affymetrix by frohike on 2007-01-12 11:26:45 as along with 10 people and 4 groups shikin rdiaz waszak jfr dchughes giovanni jeremymiller vpschulz shigepong debasis Bioinformatics G4ID GeschwindLab Genetics-of-Gambling
	Alternative splicing in the human, mouse and rat genomes is associated with an increased frequency of exon creation and/or loss. [My Copy] Nat Genet, Vol. 34, No. 2. (June 2003), pp. 177-180. by B. Modrek, C. J. Lee posted to alternative-splicing by frohike on 2007-01-12 11:16:19 as along with 2 people inesdesantiago radek
	Genome-wide detection of tissue-specific alternative splicing in the human transcriptome. [My Copy] Nucleic Acids Res, Vol. 30, No. 17. (1 September 2002), pp. 3754-3766. by Q. Xu, B. Modrek, C. Lee posted to alternative-splicing tissue by frohike on 2007-01-12 11:14:31 as along with 2 people brl antonkratz
	Genome-wide detection of alternative splicing in expressed sequences of human genes. [My Copy] Nucleic Acids Res, Vol. 29, No. 13. (1 July 2001), pp. 2850-2859. by B. Modrek, A. Resch, C. Grasso, C. Lee posted to alternative-splicing human by frohike on 2007-01-12 11:13:58 as along with 4 people and 1 group dchughes kaspermunch raylim antonkratz Bioinformatics

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