n00c's snp [59 articles] Export

Recent papers added to n00c's library classified by the tag snp. You can also see everyone's snp.

	SNP imputation in association studies [My Copy] Nature Biotechnology In Nat Biotech, Vol. 27, No. 4. (01 April 2009), pp. 349-351. by Eran Halperin, Dietrich A. Stephan posted to snp imputation gwas association by n00c on 2009-12-04 18:04:19 as along with 5 people daforerog guhjy rdiaz lwaldron psique
	Next generation sequence analysis for mitochondrial disorders. [My Copy] Genome medicine, Vol. 1, No. 10. (23 October 2009) by Valeria Vasta, Sarah B. Ng, Emily H. Turner, Jay Shendure, Si Houn H. Hahn posted to variant snp resequencing mitochondria disease database by n00c on 2009-12-04 18:03:13 as along with 1 person pst
	Genetic Variation in an Individual Human Exome [My Copy] PLoS Genet In PLoS Genet, Vol. 4, No. 8. (15 August 2008), e1000160. by Pauline C. Ng, Samuel Levy, Jiaqi Huang, et al.Timothy B. Stockwell, Brian P. Walenz, Kelvin Li, Nelson Axelrod, Dana A. Busam, Robert L. Strausberg, J. Craig Venter posted to variation snp individual-human-genome exome comparison by n00c on 2009-12-04 17:46:52 as along with 14 people Peiyong giovanni jasontsai lp2 daforerog xingxu madreach misonneh djkt bpcusack caseybrown Ema guhjy reyez
	QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data [My Copy] Nucleic Acids Research In Nucl. Acids Res., Vol. 35, No. 6. (19 March 2007), pp. 2013-2025. by Stefano Colella, Christopher Yau, Jennifer M. Taylor, et al.Ghazala Mirza, Helen Butler, Penny Clouston, Anne S. Bassett, Anneke Seller, Christopher C. Holmes, Jiannis Ragoussis posted to tool software snp quantisnp genotyping cnv bayesian by n00c on 2009-12-03 13:43:21 as along with 1 person jo_davies
	Application of massive parallel sequencing to whole genome SNP discovery in the porcine genome [My Copy] BMC Genomics, Vol. 10, No. 1. (2009), 374. by Andreia Amaral, Hendrik J. Megens, Hindrik Kerstens, et al.Henri Heuven, Bert Dibbits, Richard Crooijmans, Johan den Dunnen, Martien Groenen posted to solexa snp-discovery snp mapping illumina error-model coverage by n00c on 2009-12-03 13:17:30 as along with 3 people natstreet jsatkosk danmaclean
	Single nucleotide polymorphism (SNP) discovery in the polyploid Brassica napus using Solexa transcriptome sequencing [My Copy] Plant Biotechnology Journal, Vol. 7, No. 4. (2009), pp. 334-346. by Martin Trick, Yan Long, Jinling Meng, Ian Bancroft posted to transcriptome solexa snp-discovery snp-calling snp maqview maq illumina by n00c on 2009-12-03 13:12:16 as along with 3 people and 1 group natstreet ArtemPankin druvus Khavkin's lab
	SNPLogic: an interactive single nucleotide polymorphism selection, annotation, and prioritization system [My Copy] Nucl. Acids Res., Vol. 37, No. suppl_1. (1 January 2009), pp. D803-809. by Alexander R. Pico, Ivan V. Smirnov, Jeffrey S. Chang, et al.Ru-Fang Yeh, Joseph L. Wiemels, John K. Wiencke, Tarik Tihan, Bruce R. Conklin, Margaret Wrensch posted to website tool software snplogic snp annotation by n00c on 2009-12-03 01:02:10 as along with 3 people and 1 group daed guhjy AlexanderPico ConklinLab
	HapCUT: an efficient and accurate algorithm for the haplotype assembly problem [My Copy] Bioinformatics, Vol. 24, No. 16. (15 August 2008), pp. i153-159. by Vikas Bansal, Vineet Bafna posted to snp haplotype hapcut assembly algorithm by n00c on 2009-12-03 00:56:41 as along with 4 people dakelley maren ilyashl Neeperando
	Pyrosequencing as a method for SNP identification in the rhesus macaque (Macaca mulatta) [My Copy] BMC Genomics, Vol. 9, No. 1. (29 May 2008), 256. by Jessica Satkoski, R. S. Malhi, S. Kanthaswamy, R. Y. Tito, V. S. Malladi, D. G. Smith posted to snp-discovery snp pyrosequencing 454 by n00c on 2009-12-02 19:06:27 as along with 2 people natstreet tonia_schwartz
	SCAN: SNP and Copy number Annotation. [My Copy] Bioinformatics (Oxford, England) (17 November 2009) by Eric R. Gamazon, Wei Zhang, Anuar Konkashbaev, et al.Shiwei Duan, Emily O. Kistner, Dan L. Nicolae, M. Eileen Dolan, Nancy J. Cox posted to snp gwas genome cnv annotation by n00c on 2009-11-30 21:01:51 as along with 2 people guhjy sf11
	ssahaSNP – A Polymorphism Detection Tool by Genomic Alignment [My Copy] BMC Genomics by James C. Mullikin, Adam Spargo, Nikolai Ivanov, Mario Caccamo, Zemin Ning posted to variant-calling tool ssahasnp ssaha2 software snp-discovery snp-calling snp by n00c on 2009-11-30 14:20:33 as
	Supplementary Information - Pyrobayes: an improved base caller for SNP discovery in pyrosequences [My Copy] by Aaron R. Quinlan, Donald A. Stewart, Michael P. Strömberg, Gábor T. Marth posted to supplementary-information snp-discovery snp pyrosequencing pyrobayes 454 by n00c on 2009-11-23 00:07:37 as
	Nature Protocols: Genome resequencing and identification of variations by Illumina Genome Analyzer Reads [My Copy] by Jun Wang, Ruiqiang Li, Yingrui Li, Xiaodong Fang, Binxiao Feng, Jun Li posted to variant-calling variant solexa soapsnp snp-discovery snp resequencing illumina by n00c on 2009-11-20 20:57:20 as
	Searching for SNPs with cloud computing [My Copy] Genome Biology, Vol. 10, No. 11. (2009), R134. by Ben Langmead, Michael Schatz, Jimmy Lin, Mihai Pop, Steven Salzberg posted to soapsnp snp-discovery snp crossbow cloud-computing bowtie by n00c on 2009-11-20 20:54:53 as along with 8 people oinizan owenlancaster natstreet druvus kshameer jamesmorris jandot neils
	inGAP: an integrated next-generation genome analysis pipeline. [My Copy] Bioinformatics (Oxford, England) (30 October 2009), btp615. by Ji Qi, Fangqing Zhao, Anne Buboltz, Stephan C. Schuster posted to snp-discovery snp sequencing pipeline ingap coverage 454 by n00c on 2009-11-02 21:10:08 as along with 4 people jasontsai natstreet heliopais druvus
	Estimating population haplotype frequencies from pooled SNP data using incomplete database information [My Copy] Bioinformatics (Oxford, England) In Bioinformatics, Vol. 25, No. 24. (15 December 2009), pp. 3296-3302. by Matti Pirinen posted to snp population pooling haplotype frequency bayesian by n00c on 2009-10-30 19:22:48 as along with 1 person kshameer
	The theory of discovering rare variants via DNA sequencing [My Copy] BMC Genomics, Vol. 10, No. 1. (2009), 485. by Michael Wendl, Richard Wilson posted to variant snp-discovery snp sequencing by n00c on 2009-10-21 18:35:21 as along with 4 people jasontsai jsatkosk merpublic druvus
	Genotyping of James Watson from Low-coverage Sequencing Data [My Copy] by Sanjiv Dinakar, Yözen Hernández posted to watson snp-discovery snp-calling snp resequencing presentation genotyping coverage bayesian by n00c on 2009-10-05 16:44:36 as
	Calling Sequencing SNPs [My Copy] posted to solexa snp-calling snp illumina casava bayesian by n00c on 2009-10-02 15:38:00 as
	Discovering genetic polymorphisms in next-generation sequencing data [My Copy] Plant Biotechnology Journal, Vol. 7, No. 4. (May 2009), pp. 312-317. by Michael Imelfort, Chris Duran, Jacqueline Batley, David Edwards posted to snp-discovery snp review 2nd-generation by n00c on 2009-10-01 16:20:21 as along with 2 people orzenil darian
	Targeted single nucleotide polymorphism (SNP) discovery in a highly polyploid plant species using 454 sequencing [My Copy] Plant Biotechnology Journal, Vol. 7, No. 4. (May 2009), pp. 347-354. by Peter C. Bundock, Frances G. Eliott, Gary Ablett, et al.Adam D. Benson, Rosanne E. Casu, Karen S. Aitken, Robert J. Henry posted to snp-discovery snp sequencing polybayes plant genome 454 by n00c on 2009-10-01 16:17:51 as along with 2 people orzenil natstreet
	Single-Nucleotide Polymorphisms in Soybean [My Copy] Genetics, Vol. 163, No. 3. (1 March 2003), pp. 1123-1134. by Y. L. Zhu, Q. J. Song, D. L. Hyten, et al.C. P. Van Tassell, L. K. Matukumalli, D. R. Grimm, S. M. Hyatt, E. W. Fickus, N. D. Young, P. B. Cregan posted to snp-discovery snp polymorphism polybayes bayesian by n00c on 2009-09-28 16:55:09 as
	galign: A Tool for Rapid Genome Polymorphism Discovery [My Copy] PLoS ONE, Vol. 4, No. 9. (25 September 2009), e7188. by Shai Shaham posted to tool software snp-discovert snp polymorphism galign alignment by n00c on 2009-09-28 15:36:27 as along with 7 people and 1 group maren scmelton natstreet Benedikt_Zimmermann torfinnnome druvus stajich Mycology
	SSAHA_pileup: A Genome Variation Detection Pipeline for Various Sequencing Platforms [My Copy] by Ben Blackburne posted to ssaha_pileup snp-discovery snp presentation pileup by n00c on 2009-09-26 03:03:52 as
	ssahaSNP A Polymorphism Detection Tool on a Whole Genome Scale [My Copy] 2005 IEEE Computational Systems Bioinformatics Conference - Workshops, Vol. 0 (2005), pp. 251-254. by Zemin Ning, Mario Caccamo, James C. Mullikin posted to tool ssahasnp software snp polymorphism genome by n00c on 2009-09-26 02:39:24 as
	SNP Databases [My Copy] Single Nucleotide Polymorphisms (2009), pp. 43-71. by Christopher Phillips posted to snp-discovery snp methods database by n00c on 2009-09-26 02:01:13 as
	Pyrosequencing for SNP Genotyping [My Copy] Single Nucleotide Polymorphisms (2009), pp. 123-133. by Jose L. Royo, Jose J. Galán posted to snp-discovery snp pyrosequencing methods genotyping by n00c on 2009-09-26 01:59:51 as
	Mining SNPs from DNA Sequence Data; Computational Approaches to SNP Discovery and Analysis [My Copy] Single Nucleotide Polymorphisms, Vol. 578 (2009), pp. 73-91. by Jan Oeveren, Antoine Janssen posted to snp-discovery snp polybayes methods by n00c on 2009-09-26 01:58:28 as along with 2 people darian sandfire
	Next-Generation Sequencing Methods: Impact of Sequencing Accuracy on SNP Discovery [My Copy] Single Nucleotide Polymorphisms (2009), pp. 95-111. by Eugene Y. Chan posted to solexa snp-discovery snp resequencing repeats methods illumina helicos by n00c on 2009-09-26 01:49:02 as
	HaploSNPer: a web-based allele and SNP detection tool [My Copy] BMC Genetics, Vol. 9, No. 1. (28 February 2008), 23. by Jifeng Tang, Jack Leunissen, Roeland Voorrips, C. Gerard van der Linden, Ben Vosman posted to web tool software snp-calling snp haplosnper by n00c on 2009-09-18 18:57:07 as along with 3 people daforerog orzenil guhjy
	A Bayesian hierarchical model for analysis of SNP diversity in multilocus, multipopulation samples. [My Copy] Journal of the American Statistical Association, Vol. 104, No. 485. (1 March 2009), pp. 142-154. by Feng Guo, Dipak K. Dey, Kent E. Holsinger posted to snp bayesian by n00c on 2009-09-17 20:01:56 as along with 1 person Ayest
	novoSNP3: variant detection and sequence annotation in resequencing projects. [My Copy] Methods in molecular biology (Clifton, N.J.), Vol. 396 (2007), pp. 331-344. by P. D. Rijk, J. Del-Favero posted to tool software snp-discovery snp resequencing novosnp3 novosnp by n00c on 2009-09-17 19:56:56 as along with 1 person csrocha
	novoSNP, a novel computational tool for sequence variation discovery [My Copy] Genome Research, Vol. 15, No. 3. (March 2005), pp. 436-442. by Stefan Weckx, Jurgen Del-Favero, Rosa Rademakers, et al.Lieve Claes, Marc Cruts, Peter De Jonghe, Christine Van Broeckhoven, Peter De Rijk posted to variant tool snp-discovery snp polybayes novosnp by n00c on 2009-09-17 19:55:13 as along with 4 people csrocha daforerog Ayest farhat
	SNP-PHAGE - High throughput SNP discovery pipeline [My Copy] BMC Bioinformatics, Vol. 7, No. 1. (23 October 2006), 468. by Lakshmi Matukumalli, John Grefenstette, David Hyten, Ik Y. Choi, Perry Cregan, Curtis Van Tassell posted to tool snp-phage snp-discovery snp-calling snp pipeline machine-learning by n00c on 2009-09-17 19:53:45 as along with 6 people sandfire csrocha daforerog natstreet druvus guhjy
	SNPdetector: a software tool for sensitive and accurate SNP detection. [My Copy] PLoS computational biology, Vol. 1, No. 5. (28 October 2005), e53. by Jinghui Zhang, David A. Wheeler, Imtiaz Yakub, et al.Sharon Wei, Raman Sood, William Rowe, Paul P. Liu, Richard A. Gibbs, Kenneth H. Buetow posted to tool software snpdetector snp-calling snp nqs by n00c on 2009-09-17 19:51:00 as along with 4 people csrocha natstreet druvus Ayest
	dbSNP: the NCBI database of genetic variation [My Copy] Nucl. Acids Res., Vol. 29, No. 1. (1 January 2001), pp. 308-311. by S. T. Sherry, M. H. Ward, M. Kholodov, et al.J. Baker, L. Phan, E. M. Smigielski, K. Sirotkin posted to tpgp snp-discovery snp dbsnp database by n00c on 2009-09-17 19:41:33 as along with 4 people and 1 group daforerog aalibes fisherp massivemayhem References for 3DSim paper
	SNP-finding example with Ant transcript reads - Bioinformatics Core Wiki [My Copy] posted to transcriptome snp-discovery snp newbler gsmapper gigabayes 454 by n00c on 2009-09-14 16:32:08 as
	dbSNP and HapMap Data [My Copy] posted to snp hapmap faq dbsnp by n00c on 2009-09-14 01:11:07 as
	An SNP map of the human genome generated by reduced representation shotgun sequencing [My Copy] Nature, Vol. 407, No. 6803. (28 September 2000), pp. 513-516. by David Altshuler, Victor J. Pollara, Chris R. Cowles, et al.William J. Van Etten, Jennifer Baldwin, Lauren Linton, Eric S. Lander posted to snp-discovery snp-calling snp nqs by n00c on 2009-09-13 22:20:10 as along with 2 people jlin lpanunzi
	New strategy to detect single nucleotide polymorphisms. [My Copy] Genetics and molecular research : GMR, Vol. 5, No. 1. (31 March 2006), pp. 143-153. by Miguel Galves, José Augusto Amgarten A. Quitzau, Zanoni Dias posted to snp-discovery snp-calling snp algorithm by n00c on 2009-09-13 09:23:02 as along with 1 person Ayest
	SNP discovery using advanced algorithms and neural networks [My Copy] Bioinformatics, Vol. 21, No. 10. (15 May 2005), pp. 2528-2530. by Per Unneberg, Michael Stromberg, Fredrik Sterky posted to tool software snp-discovery snp neural-network forage algorithm by n00c on 2009-09-13 07:27:20 as along with 1 group Daniel
	Genome-wide analysis of single-nucleotide polymorphisms in human expressed sequences [My Copy] Nat Genet, Vol. 26, No. 2. (01 October 2000), pp. 233-236. by Kris Irizarry, Vlad Kustanovich, Cheng Li, et al.Nik Brown, Stanley Nelson, Wing Wong, Christopher J. Lee posted to snp-calling snp genome bayesian by n00c on 2009-09-13 07:13:33 as along with 1 person slevy03
	Quality and completeness of SNP databases [My Copy] Nature Genetics, Vol. 33, No. 4. (24 March 2003), pp. 457-458. by David E. Reich, Stacey B. Gabriel, David Altshuler posted to snp resequencing database by n00c on 2009-09-12 18:32:13 as along with 2 people jsatkosk farhat
	PolyBayes [My Copy] by Ruslan Salakhutdinov posted to snp-calling snp pyrobayes primer presentation polybayes bayesian 454 by n00c on 2009-09-11 20:10:20 as
	A general approach to single-nucleotide polymorphism discovery [My Copy] Nat Genet, Vol. 23, No. 4. (December 1999), pp. 452-456. by Gabor T. Marth, Ian Korf, Mark D. Yandell, et al.Raymond T. Yeh, Zhijie Gu, Hamideh Zakeri, Nathan O. Stitziel, Ladeana Hillier, Pui-Yan Kwok, Warren R. Gish posted to snp-discovery snp-calling snp polybayes bayesian by n00c on 2009-09-03 16:28:35 as along with 4 people and 1 group gpappas Ayest azazello farhat gatech-compgenomics
	PineSAP--sequence alignment and SNP identification pipeline [My Copy] Bioinformatics, Vol. 25, No. 19. (1 October 2009), pp. 2609-2610. by Jill L. Wegrzyn, Jennifer M. Lee, John Liechty, David B. Neale posted to software snp-calling snp resequencing pipeline pinesap machine-learning alignment by n00c on 2009-08-17 01:57:22 as along with 7 people jasontsai jsatkosk daforerog djkt operon nuin druvus
	High-throughput genotyping by whole-genome resequencing. [My Copy] Genome research, Vol. 19, No. 6. (6 June 2009), pp. 1068-1076. by Xuehui Huang, Qi Feng, Qian Qian, et al.Qiang Zhao, Lu Wang, Ahong Wang, Jianping Guan, Danlin Fan, Qijun Weng, Tao Huang, Guojun Dong, Tao Sang, Bin Han posted to genotyping resequencing snp snp-calling by n00c on 2009-08-07 02:36:21 as along with 9 people APRegier jandot reyez sandfire djkt natstreet jbhiatt GeeSharpMinor langmead
	Detection of single nucleotide variations in expressed exons of the human genome using RNA-Seq [My Copy] Nucl. Acids Res., Vol. 37, No. 16. (1 September 2009), e106. by Iouri Chepelev, Gang Wei, Qingsong Tang, Keji Zhao posted to rna-seq snp snv transcriptome by n00c on 2009-07-31 17:54:00 as along with 6 people and 1 group hzoltan woodson8 guhjy fenghezi ghattem GeeSharpMinor SIMR bioinformatics
	Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding [My Copy] Genome Research, Vol. 19, No. 9. (22 September 2009), pp. 1527-1541. by Kevin J. McKernan, Heather E. Peckham, Gina L. Costa, et al.Stephen F. McLaughlin, Yutao Fu, Eric F. Tsung, Christopher R. Clouser, Cisyla Duncan, Jeffrey K. Ichikawa, Clarence C. Lee, Zheng Zhang, Swati S. Ranade, Eileen T. Dimalanta, Fiona C. Hyland, Tanya D. Sokolsky, Lei Zhang, Andrew Sheridan, Haoning Fu, Cynthia L. Hendrickson, Bin Li, Lev Kotler, Jeremy R. Stuart, Joel A. Malek, Jonathan M. Manning, Alena A. Antipova, Damon S. Perez, Michael P. Moore, Kathleen C. Hayashibara, Michael R. Lyons, Robert E. Beaudoin, Brittany E. Coleman, Michael W. Laptewicz, Adam E. Sannicandro, Michael D. Rhodes, Rajesh K. Gottimukkala, Shan Yang, Vineet Bafna, Ali Bashir, Andrew MacBride, Can Alkan, Jeffrey M. Kidd, Evan E. Eichler, Martin G. Reese, Francisco M. De La Vega, Alan P. Blanchard posted to variant tpgp solid snp-calling snp resequencing abi by n00c on 2009-07-29 18:04:49 as along with 17 people hzoltan gbenson adijr chrisamiller heliopais daforerog druvus djkt psique sameersoi APRegier fenghezi jmanning2k xingxu pkonings jandot natstreet
	The complete genome of an individual by massively parallel DNA sequencing. [My Copy] Nature, Vol. 452, No. 7189. (17 April 2008), pp. 872-876. by David A. Wheeler, Maithreyan Srinivasan, Michael Egholm, et al.Yufeng Shen, Lei Chen, Amy McGuire, Wen He, Yi-Ju Chen, Vinod Makhijani, G. Thomas Roth, Xavier Gomes, Karrie Tartaro, Faheem Niazi, Cynthia L. Turcotte, Gerard P. Irzyk, James R. Lupski, Craig Chinault, Xing-zhi Song, Yue Liu, Ye Yuan, Lynne Nazareth, Xiang Qin, Donna M. Muzny, Marcel Margulies, George M. Weinstock, Richard A. Gibbs, Jonathan M. Rothberg posted to watson tpgp snp resequencing pyrosequencing individual-human-genome genome 454 by n00c on 2009-07-28 18:47:35 as along with 23 people and 2 groups rshe jonilaserson jessopher daforerog behindtherabbit frohike reyez pengchy adijr jo_davies jfr orzenil dullhunk djkt ramensky psique caseybrown melting dbensasson bpb Neeperando Huub_odc guhjy parkinson's disease references microbiology_nijmegen

Note: You may cite this page as: http://www.citeulike.org/user/n00c/tag/snp

Result page: 1 2 Next

short-read	99
algorithm	94
software	87
tool	66
genome	64
sequencing	61
snp	59
454	52
map	51
resequencing	51
assembly	49
alignment	45
snp-discovery	38
solexa	35
illumina	35
rna-seq	29
snp-calling	29
review	29
tandem-repeats	28
sequence	20
data-structure	20
transcriptome	19
de-novo	16
pyrosequencing	16
burrows-wheeler	16
assembler	16
tpgp	15
bayesian	15
variant	14
string-matching	14
vntr	14
pipeline	13
individual-human-genome	12
error-model	12
visualization	12
web-service	12
comparison	12
mosaik	11
indexing	11
repeats	11
abi	10
error-bound	10
solid	10
viewer	10
lcs	9
cnv	9
bioinformatics	9
microarray	9
base-calling	9
suffix-array	9
quality	9
coverage	8
suffix-tree	8
enrichment	8
paired-end	8
variation	8
database	8
polybayes	8
error	7
mapping	7
capture	7
genotyping	7
library	6
tandem	6
dna	6
presentation	6
sv	6
disease	6
association	6
genomics	6
graph	5
li	5
methods	5
tree	5
suffix	5
multiplexing	5
bowtie	5
gigabayes	5
jennifer-beane	5
maq	5
web	5
longevity	5
seqman	5
biology	4
variant-calling	4
fm-index	4
clc	4
cloud-computing	4
enhanced-suffix-array	4
newbler	4
text	4
color-space	4
soap	4
book	4
bu	4
roche	4
data	4
pyrobayes	4
mutation	4
3rd-generation	4
machine-learning	4
structure	4
venter	4
compression	4
polymorphism	4
pool-design	4
pool	4
sff	4
haplotype	4
copy-number	4
bacterial	4
aging	3
research	3
annotation	3
space	3
soapsnp	3
de-brujin	3
ssahasnp	3
gwas	3
format	3
exome	3
celera	3
landau	3
centenarian	3
lbi	3
r	3
differential-gene-expression	3
vishkin	3
workflow	3
bwa	3
helicos	3
nqs	3
human	3
ace	3
bias	3
browser	3
statistics	3
open-source	3
nd	2
segemehl	2
rmap	2
tutorial	2
snp-discovert	2
tfs	2
haskell	2
virus	2
combinatorics	2
validation	2
hapmap	2
biomoby	2
technology	2
navarro	2
huref	2
asian	2
microbial_genetics	2
est	2
linux	2
aml	2
trf	2
consensus	2
abyss	2
staden	2
gene-expression	2
human-genome	2
venn-diagram	2
alta-cyclic	2
ssake	2
registry	2
organization	2
gap4	2
erange	2
single-molecule	2
parallel	2
vcake	2
low-complexity	2
diagnostics	2
nussinov	2
rolexa	2
cplusplus	2
allpaths	2
mouse	2
list	2
lecroq	2
bloom-filter	2
2nd-generation	2
bioconductor	2
shore	2
methodology	2
pdf	2
bumc	2
gpu	2
multiple-alignment	2
leukemia	2
eulerian	2
file	2
np-complete	2
seed	2
arachne	2
novosnp	2
nakatsu	2
gff	2
ssaha2	2
user-group	2
gui	2
flowgram	2
genetics	2
structural-variation	2
liver	2
sudoku	2
durbin	2
report	2
graph-theory	2
watson	2
dbsnp	2
frequency	2
cap3	2
apple	2
dust	2
phred	2
maximum-likelihood	1
pacific-biosciences	1
textbook	1
reconciliation	1
snv	1
meiosis	1
pass	1
planet	1
survey	1
gastroenteritis	1
pooling	1
1000-genomes	1
soap2	1
reputer	1
pairwise	1
alleles	1
splice	1
pinesap	1
contig	1
extended-suffix-array	1
tools	1
mapper	1
arabidopsis	1
allpaths2	1
igraph	1
error-rate	1
gene-enrichment	1
faq	1
pileup	1
genome-browser	1
recombination	1
gr-aligner	1
maqgene	1
eagleview	1
shortread	1
misassembly	1
blast	1
poster	1
broad-institute	1
simulation	1
qsra	1
kautz-zeckendorf	1
breakdancer	1
sage	1
pooled	1
fastq	1
meeting	1
hash	1
patman	1
multiplex	1
tagdust	1
imputation	1
asssembly	1
samtools	1
casava	1
supplementary-information	1
personal-genomics	1
gamma-distribution	1
survival	1
bank	1
ruby	1
junction	1
bibliography	1
social	1
analysis	1
conference	1
maqview	1
rna-mate	1
bound	1
shotgun	1
provenance	1
pet	1
mask	1
tophat	1
tileqc	1
snplogic	1
shoremap	1
greed	1
mrna	1
genome-sequencer-flx	1
str	1
tandem-repeat-finder	1
transcription	1
mapview	1
ssaha_pileup	1
string-scanning	1
boyer-moore	1
matlab	1
errors	1
exon-capture	1
array	1
seqan	1
website	1
semantic-web	1
stat5a	1
primer	1
alphabet	1
snp-o-matic	1
local	1
promoter	1
subsequence	1
rna	1
exon	1
k-means	1
gigassembler	1
socs	1
disorder	1
mom	1
datamining	1
inference	1
ncbi	1
exonerate	1
asymptotic	1
bachmann-landau	1
cluster	1
windowmasker	1
hawkeye	1
genetic_association_studies	1
forage	1
pindel	1
firefox	1
order	1
minisatellites	1
string	1
mendeley	1
ebi	1
genotype	1
gap	1
palindromes	1
difference	1
varscan	1
novosnp3	1
nimblegen	1
qpalma	1
indel	1
yh	1
swap454	1
plugin	1
f-seq	1
framework	1
web-server	1
tview	1
laboratory	1
subquadratic	1
mrfast	1
shrimp	1
ngsview	1
mitochondria	1
ucsc	1
target-region	1
arachne2	1
polyfreq	1
pemer	1
hirschberg	1
factor-oracle	1
toolkit	1
pruning	1
euler	1
q-gram	1
wiki	1
piqa	1
unofficial	1
dynamic-programming	1
tile	1
sff_extract	1
toronto-2008	1
semantic	1
pachter	1
smith-waterman	1
population	1
myexperiment	1
heatmap	1
bwt-sw	1
findpeaks	1
repeat	1
model	1
hunt-szymanski	1
mvf	1
iphone	1
bustard	1
transcriptomics	1
sam	1
scaffold	1
trbase	1
semi-global	1
gnumap	1
path	1
oslay	1
bfast	1
yoruba	1
galign	1
set	1
diversity	1
translocation	1
links	1
viewing	1
cloudburst	1
cabog	1
scaffolding	1
programming	1
jbrowse	1
fm-kz	1
biomart	1
file-format	1
mutations	1
blat	1
sanger	1
connected-component	1
phusion	1
protocol	1
breakpoint	1
barcoding	1
breakpoints	1
gsmapper	1
bwt	1
element	1
computer-science	1
function	1
false-positive	1
lasergene	1
razers	1
quantisnp	1
avid	1
mailing-list	1
lectures	1
lookseq	1
prediction	1
eland	1
swift	1
velvet	1
forum	1
in-silico	1
guide	1
finite-automaton	1
suffix-stree	1
papers	1
slider	1
plant	1
reps	1
cdna	1
consed	1
semi-local	1
cancer	1
hi	1
snp-phage	1
caf	1
genotyping-errors	1
color	1
probhd	1
scripting	1
myers	1
expression	1
neural-network	1
ssaha	1
hnf4alpha	1
newsarticle	1
agilent	1
pts	1
mobyle	1
shorty	1
bayescall	1
mining	1
hapcut	1
polymerase	1
python	1
notation	1
salzberg	1
cnv-seq	1
oasis	1
real-time	1
network	1
mummer	1
palma	1
sickle-cell	1
dibase	1
t-reks	1
zoom	1
minisatellite	1
perm	1
trap	1

n00c's snp [59 articles] Export

n00c's tags