jsatkosk's cnv [8 articles] Export

Recent papers added to jsatkosk's library classified by the tag cnv. You can also see everyone's cnv.

	Population genetic models of duplicated genes. [My Copy] Genetica, Vol. 137, No. 1. (1 September 2009), pp. 19-37. by Hideki Innan posted to cnv by jsatkosk on 2009-07-29 19:55:40 as along with 1 person sameersoi
	Genomic Drift and Evolution of Microsatellite DNAs in Human Populations [My Copy] Mol Biol Evol, Vol. 26, No. 8. (1 August 2009), pp. 1835-1840. by Naoko Takezaki, Masatoshi Nei posted to cnv human microsatellite by jsatkosk on 2009-07-29 19:51:29 as along with 4 people Fuzzer sameersoi nuin aprasad
	A procedure for highly specific, sensitive, and unbiased whole-genome amplification [My Copy] Proceedings of the National Academy of Sciences, Vol. 105, No. 40. (7 October 2008), pp. 15499-15504. by Xinghua Pan, Alexander E. Urban, Dean Palejev, et al.Vincent Schulz, Fabian Grubert, Yiping Hu, Michael Snyder, Sherman M. Weissman posted to amplification cnv genome snp whole by jsatkosk on 2009-06-11 22:12:37 as along with 3 people pkonings lusk Katje
	The success of the genome-wide association approach: a brief story of a long struggle [My Copy] European Journal of Human Genetics, Vol. aop, No. current. by Ku C. Seng, Chia K. Seng posted to association cnv disease genome haplotype hapmap linkage snp wide by jsatkosk on 2009-06-09 18:52:38 as along with 2 people xingxu guhjy
	Single nucleotide polymorphism (SNP) discovery in duplicated genomes: intron-primed exon-crossing (IPEC) as a strategy for avoiding amplification of duplicated loci in Atlantic salmon (Salmo salar) and other salmonid fishes [My Copy] BMC Genomics, Vol. 7 (27 July 2006), 192. by Heikki J. Ryynanen, Craig R. Primmer posted to cnv discovery intron sequence snp by jsatkosk on 2009-06-05 23:16:54 as along with 1 person Terkko
	Population analysis of large copy number variants and hotspots of human genetic disease. [My Copy] American journal of human genetics, Vol. 84, No. 2. (22 February 2009), pp. 148-161. by Andy Itsara, Gregory M. Cooper, Carl Baker, et al.Santhosh Girirajan, Jun Li, Devin Absher, Ronald M. Krauss, Richard M. Myers, Paul M. Ridker, Daniel I. Chasman, Heather Mefford, Phyllis Ying, Deborah A. Nickerson, Evan E. Eichler posted to cnv disease mutation population by jsatkosk on 2009-06-05 22:11:51 as along with 8 people and 1 group daforerog turnersd sameersoi guhjy Zephyrus pkonings jdbowes psique Roswell Cancer Crosstalk
	Estimating the number of unseen variants in the human genome. [My Copy] Proceedings of the National Academy of Sciences of the United States of America, Vol. 106, No. 13. (31 March 2009), pp. 5008-5013. by I. Ionita-Laza, C. Lange, N. M Laird posted to algorithm cnv sequencing snp by jsatkosk on 2009-06-05 22:08:56 as along with 5 people giovanni TRHvidsten pkonings guhjy benjaminsb
	Joint estimation of copy number variation and reference intensities on multiple DNA arrays using GADA. [My Copy] Bioinformatics (Oxford, England), Vol. 25, No. 10. (15 May 2009), pp. 1223-1230. by R. Pique-Regi, A. Ortega, S. Asgharzadeh posted to cnv dna microarray by jsatkosk on 2009-06-05 22:06:27 as along with 5 people jfr guhjy humburg pkonings rdiaz

Note: You may cite this page as: http://www.citeulike.org/user/jsatkosk/tag/cnv

CiteULike organises scholarly (or academic) papers or literature and provides bibliographic (which means it makes bibliographies) for universities and higher education establishments. It helps undergraduates and postgraduates. People studying for PhDs or in postdoctoral (postdoc) positions. The service is similar in scope to EndNote or RefWorks or any other reference manager like BibTeX, but it is a social bookmarking service for scientists and humanities researchers.

snp	40
disease	15
association	14
linkage	14
dna	12
genome	11
algorithm	10
discovery	9
population	9
cnv	8
degraded	8
genotype	7
human	7
macaque	7
primate	7
sequencing	7
microsatellite	6
whole	6
forensic	5
genetics	5
diversity	4
gene	4
genotyping	4
microarray	4
mulatta	4
mutation	4
pcr	4
quantitative	4
sequence	4
alignment	3
analysis	3
asthma	3
fascicularis	3
feces	3
genetic	3
hapmap	3
phenotype	3
aim	2
bioinformatics	2
cross-species	2
error	2
heterozygosity	2
identification	2
inconsistency	2
mapping	2
mirna	2
mitochondria	2
phylogeny	2
polymorphism	2
qtl	2
rate	2
reduced	2
representation	2
structure	2
study	2
wide	2
abo	1
admixture	1
ambiguous	1
amplification	1
bioperl	1
blood	1
browser	1
by	1
canine	1
component	1
conservation	1
database	1
distance	1
drift	1
expression	1
flanking	1
flow	1
functional	1
groups	1
haplotype	1
heteroplasmy	1
hybridization	1
indel	1
intron	1
introns	1
isolation	1
landscape	1
library	1
lvh	1
malaria	1
mtdna	1
nih	1
nuclear	1
of	1
pedigree	1
pigmentation	1
principal	1
pyrosequencing	1
real-time	1
recombination	1
region	1
research	1
rna	1
sampling	1
sex	1
siv	1
speciation	1
statistics	1
taqman	1
vaccine	1
virus	1
wild	1

jsatkosk's cnv [8 articles] Export

jsatkosk's tags