frohike's cnv [12 articles] Export

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	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 copy-number-variation normal human_genome 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
	Personalized copy number and segmental duplication maps using next-generation sequencing. [My Copy] Nature genetics, Vol. 41, No. 10. (30 October 2009), pp. 1061-1067. by Can Alkan, Jeffrey M. Kidd, Tomas Marques-Bonet, et al.Gozde Aksay, Francesca Antonacci, Fereydoun Hormozdiari, Jacob O. Kitzman, Carl Baker, Maika Malig, Onur Mutlu, S. Cenk Sahinalp, Richard A. Gibbs, Evan E. Eichler posted to second_generation_sequencing personalized_medicine cnv by frohike on 2009-08-31 11:23:12 as along with 30 people and 1 group ongenetics chvlyl leemachado daed gbenson n00c bozdagd dakelley sbmontgomery eshirdel merpublic shyamsg scmelton qayub natstreet fenghezi Annab djkt nuin xingxu jamesmorris rdiaz brant torfinnnome jandot pkonings danmaclean daforerog rschulz gangcai Journal picks
	Common Regulatory Variation Impacts Gene Expression in a Cell Type-Dependent Manner [My Copy] Science, Vol. 325, No. 5945. (4 September 2009), pp. 1246-1250. by Antigone S. Dimas, Samuel Deutsch, Barbara E. Stranger, et al.Stephen B. Montgomery, Christelle Borel, Homa Attar-Cohen, Catherine Ingle, Claude Beazley, Maria G. Arcelus, Magdalena Sekowska, Marilyne Gagnebin, James Nisbett, Panos Deloukas, Emmanouil T. Dermitzakis, Stylianos E. Antonarakis posted to cell_type cnv eqtl gene_expression regulatory_variation snp tissue_specific by frohike on 2009-08-06 10:20:48 as along with 12 people vplagnol cajunsushi ajbattle xianjun kintoki TRHvidsten djkt fenghezi rdiaz humburg guhjy SeaBird
	High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applications [My Copy] Genome Research, Vol. 19, No. 9. (10 September 2009), pp. 1682-1690. by Tamim H. Shaikh, Xiaowu Gai, Juan C. Perin, et al.Joseph T. Glessner, Hongbo Xie, Kevin Murphy, Ryan O'Hara, Tracy Casalunovo, Laura K. Conlin, Monica D'Arcy, Edward C. Frackelton, Elizabeth A. Geiger, Chad Haldeman-Englert, Marcin Imielinski, Cecilia E. Kim, Livija Medne, Kiran Annaiah, Jonathan P. Bradfield, Elvira Dabaghyan, Andrew Eckert, Chioma C. Onyiah, Svetlana Ostapenko, F. George Otieno, Erin Santa, Julie L. Shaner, Robert Skraban, Ryan M. Smith, Josephine Elia, Elizabeth Goldmuntz, Nancy B. Spinner, Elaine H. Zackai, Rosetta M. Chiavacci, Robert Grundmeier, Eric F. Rappaport, Struan F. A. Grant, Peter S. White, Hakon Hakonarson posted to copy-number-variation for:pkonings databases database_genomic_variants cnv cgh by frohike on 2009-08-06 10:07:27 as along with 7 people rdiaz pkonings ericrpaquet jandot guhjy vplagnol daforerog
	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 copy-number-variation arraycgh benign cnv human malignant review by frohike on 2008-11-04 11:10:34 as along with 3 people and 1 group brianb misonneh Zephyrus Roswell Cancer Crosstalk
	Microarray analysis reveals a major direct role of DNA copy number alteration in the transcriptional program of human breast tumors. [My Copy] Proceedings of the National Academy of Sciences of the United States of America, Vol. 99, No. 20. (1 October 2002), pp. 12963-12968. by Jonathan R. Pollack, Therese Sørlie, Charles M. Perou, et al.Christian A. Rees, Stefanie S. Jeffrey, Per E. Lonning, Robert Tibshirani, David Botstein, Anne-Lise L. Børresen-Dale, Patrick O. Brown posted to breast-cancer arraycgh cdna cnv microarray_technology by frohike on 2008-11-04 11:03:42 as along with 3 people shikin rdiaz bioguru2000
	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 cnv gene_expression 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
	Human genomics: In search of normality [My Copy] Nature, Vol. 444, No. 7118. (22 November 2006), pp. 428-429. by Kevin V. Shianna, Huntington F. Willard posted to copy-number-variation cnv comment by frohike on 2008-08-08 10:16:04 as
	Genomic and transcriptional aberrations linked to breast cancer pathophysiologies [My Copy] Cancer Cell, Vol. 10, No. 6. (December 2006), pp. 529-541. by Koei Chin, Sandy Devries, Jane Fridlyand, et al.Paul T. Spellman, Ritu Roydasgupta, Wen-Lin Kuo, Anna Lapuk, Richard M. Neve, Zuwei Qian, Tom Ryder posted to copy-number-variation breast-cancer cnv arraycgh by frohike on 2008-08-08 10:04:05 as along with 4 people engelhardt oelemento jfr chrisamiller
	Genotype, haplotype and copy-number variation in worldwide human populations. [My Copy] Nature, Vol. 451, No. 7181. (21 February 2008), pp. 998-1003. by Mattias Jakobsson, Sonja W. Scholz, Paul Scheet, et al.J. Raphael Gibbs, Jenna M. VanLiere, Hon-Chung C. Fung, Zachary A. Szpiech, James H. Degnan, Kai Wang, Rita Guerreiro, Jose M. Bras, Jennifer C. Schymick, Dena G. Hernandez, Bryan J. Traynor, Javier Simon-Sanchez, Mar Matarin, Angela Britton, Joyce van de Leemput, Ian Rafferty, Maja Bucan, Howard M. Cann, John A. Hardy, Noah A. Rosenberg, Andrew B. Singleton posted to cnv genotype haplotype human population snp by frohike on 2008-08-08 08:55:38 as along with 15 people and 2 groups misonneh vplagnol turnersd daforerog sameersoi psique ilyashl Zephyrus djkt ramensky mailund thomaskelder Archaeogenetics jo_davies guhjy Roswell Cancer Crosstalk Fasting, food and evolution
	Global variation in copy number in the human genome [My Copy] 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 cnv by frohike on 2007-01-12 11:27:09 as along with 41 people and 7 groups 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

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breast-cancer	224
microarray	100
bayesian-network	66
ovarian_cancer	50
microarray_data_analysis	50
arraycgh	42
proteomics	42
network	36
database	33
microrna	31
signature	30
prognosis	29
review	26
software	24
sequencing	24
mirna	24
microarray_data	23
integration	22
lung_cancer	22
snp	20
cancer	19
human	18
epigenomics	18
regulatory	17
methylation	17
pathway	17
mass_spectrometry	17
survival	16
mutation	16
rectal_cancer	16
classification	15
clustering	15
biomarker	14
cetuximab	13
second_generation_sequencing	13
data_integration	13
metabolomics	13
disease	13
tissue_specific	13
cnv	12
copy-number-variation	12
signatures	12
tool	12
protein	12
treatment	12
protein_interaction_network	12
drug	11
methylome	11
seldi	11
priors	10
affymetrix	10
mirna_target_prediction	10
brca1	10
online	10
alternative-splicing	10
svm	10
microarray_technology	9
genetic	9
gene	9
interaction	9
systems_biology	9
ismb2008	9
validation	9
comment	9
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pathways	8
gsea	8
cdna	8
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metastasis	8
book	8
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familial_ovarian_cancer	8
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egfr	7
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maldi	7
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colon	5
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geneset	4
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dynamic	4
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myc	4
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kernel	4
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sam	4
glioblastoma	4
for:jfr	4
brca2	4
bioconductor	4
interactions	4
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omics	3
oncogene	3
stem_cell	3
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naive	3
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file-import-08-11-18	3
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mouse	3
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ai	3
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idtranslation	3
grade	3
platin	3
basal	3
aracne	3
genomics	3
expo	3
solexa	2
ovacheck	2
bind	2
mirna_activity_score	2
missing	2
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tensor	2
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kras	2
psb2008	2
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hprd	2
cancer_network	2
cost	2
vegf	2
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variable	2
kegg	2
prostate_cancer	2
brca	2
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st	2
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conventional	2
pptc	2
her2	2
mmp9	2
webtool	2
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miranda	2
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hupo	2
syntren	2
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synergy	2
ncor1	2
crohn	2
gcrma	2
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nbr1	2
differential-equation	2
robo1	2
svd	2
normal_expression	2
serum	2
graph	2
fibroblast	2
learning	2
chip_chip	2
intact	2
mas5	2
fdr	2
aberration	2
medical_decision_support	2
transcriptome	2
editorial	2
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genetics	2
kinase	2
transbig	2
e-coli	2
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loss	2
performance	2
permutation	2
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imaging	2
models	2
ggi	2
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tap	2
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r	2
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itraq	1
aml	1
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brain	1
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454	1
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ontology	1
textbook	1
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gaussian_graph	1
ascites	1
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pam	1
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atherosclerosis	1
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p	1
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alc1	1
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vib	1
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nfkb1	1
stemmer	1
solid	1
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carlo	1
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signature_candidate	1
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parp_inhibitor	1
omicsnetworks	1
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rt_pcr	1
gene_ontology	1
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vision	1
gap_statistic	1
java	1
hiv	1
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igs	1
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nerve_fiber	1
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uk	1
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ct	1
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veer	1
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dream	1
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signs	1
kidney_cancer	1
translocation	1
tamoxifen	1
passenger_mutation	1
human_genome	1
party_hub	1

frohike's cnv [12 articles] Export

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