nmohelli's library 17 articles Export

	De novo bacterial genome sequencing: Millions of very short reads assembled on a desktop computer [My Copy] Genome Research, Vol. 18, No. 5. (10 May 2008), pp. 802-809. by David Hernandez, Patrice FranÃ§ois, Laurent Farinelli, Magne Ãsterã¥s, Jacques Schrenzel posted to assembly short-reads soft software by nmohelli on 2009-01-06 13:46:43 as along with 15 people and 4 groups n00c GeeSharpMinor pachorip operon druvus dakelley acn GustavoLacerda jmeppley stajich azazello Katje iris42 balicea Neeperando DeNovoAssembly-SIMR microbiology_nijmegen Mycology gatech-compgenomics
	De novo fragment assembly with short mate-paired reads: Does the read length matter? [My Copy] Genome research, Vol. 19, No. 2. (3 February 2009), pp. 336-346. by Mark J. Chaisson, Dumitru Brinza, Pavel A. Pevzner posted to assembling short-reads software by nmohelli on 2008-12-18 09:21:44 as along with 18 people and 1 group darian n00c carlk APRegier jandot jonilaserson natstreet dakelley jessopher orzenil AaronDarling sphsmith jasontsai jbhiatt druvus hpaces GustavoLacerda stajich Mycology
	SHARCGS, a fast and highly accurate short-read assembly algorithm for de novo genomic sequencing. [My Copy] Genome research, Vol. 17, No. 11. (November 2007), pp. 1697-1706. by J. C. Dohm, C. Lottaz, T. Borodina, H. Himmelbauer posted to assembly short-reads by nmohelli on 2008-12-03 17:09:23 as along with 16 people and 2 groups operon n00c robsyme dakelley acn druvus natstreet timflutre stajich ghattem azazello GustavoLacerda niallhaslam flexer jwhitney iris42 DeNovoAssembly-SIMR Mycology
	d2_cluster: A Validated Method for Clustering EST and Full-Length cDNA Sequences [My Copy] Genome Research, Vol. 9, No. 11. (1 November 1999), pp. 1135-1142. by John Burke, Dan Davison, Winston Hide posted to clustering est by nmohelli on 2008-11-12 13:18:04 as along with 3 people nwpuzebra sficklin urgi
	Optimal spliced alignments of short sequence reads [My Copy] Bioinformatics, Vol. 24, No. 16. (15 August 2008), pp. i174-180. by Fabio De Bona, Stephan Ossowski, Korbinian Schneeberger, Gunnar Ratsch posted to qpalma short-reads by nmohelli on 2008-10-17 15:03:47 as along with 12 people and 1 group GustavoLacerda darshan n00c natstreet druvus lukaswindhager malcook jmcq caseybrown cthachuk Ema Neeperando SIMR bioinformatics
	Consensus generation and variant detection by Celera Assembler [My Copy] Bioinformatics (Oxford, England) In Bioinformatics, Vol. 24, No. 8. (15 April 2008), pp. 1035-1040. by Gennady Denisov, Brian Walenz, Aaron L. Halpern, et al.Jason Miller, Nelson Axelrod, Samuel Levy, Granger Sutton posted to assembling snp by nmohelli on 2008-10-17 14:42:39 as along with 7 people darian n00c dakelley orzenil natstreet druvus semrich
	Velvet: Algorithms for de novo short read assembly using de Bruijn graphs [My Copy] Genome Research In Genome Research, Vol. 18, No. 5. (18 May 2008), pp. 821-829. by Daniel R. Zerbino, Ewan Birney posted to assembly short-reads software by nmohelli on 2008-10-17 14:19:33 as along with 42 people and 3 groups ajsferreira vplagnol bedo jwhitney cthachuk hzoltan azazello ajbattle jmanning2k n00c carlk pachorip APRegier jbhiatt jonilaserson operon jahwa jsatkosk sandfire thegoose2 katholt robsyme djkt hpaces AaronDarling mhz idoerg jmcq dswan dakelley jasontsai acn druvus natstreet stajich farhat iris42 tharris Neeperando sharpton GustavoLacerda gdb Bioinformatics DeNovoAssembly-SIMR Mycology
	Haplotype inference from unphased SNP data in heterozygous polyploids based on SAT [My Copy] BMC Genomics, Vol. 9 (30 July 2008), 356. by Jost Neigenfind, Birgit Kersten, Rico Basekow, et al.Joachim Selbig, Christiane Gebhardt, Gabor Gyetvai, Ute Achenbach, Svenja Diehl posted to haplotype inference snp by nmohelli on 2008-10-17 14:03:10 as along with 1 person jfsevilla
	Mapping short DNA sequencing reads and calling variants using mapping quality scores. [My Copy] Genome research, Vol. 18, No. 11. (19 November 2008), pp. 1851-1858. by Heng Li, Jue Ruan, Richard Durbin posted to short-reads by nmohelli on 2008-10-17 13:02:33 as along with 38 people and 2 groups seninp heliopais hzoltan cthachuk darshan adijr darian bozdagd jmanning2k stubrown APRegier ghattem jbhiatt mmartin michaelbarton polivares jonilaserson humburg n00c jessopher maren GeeSharpMinor vmsr vplagnol natstreet poschm jfr druvus dandaman xingxu rschulz jmcq inesdesantiago Neeperando matthewsuderman bpb gdb farhat SIMR bioinformatics BergmanLab
	Assembling millions of short DNA sequences using SSAKE [My Copy] Bioinformatics, Vol. 23, No. 4. (15 February 2007), pp. 500-501. by Rene L. Warren, Granger G. Sutton, Steven J. M. Jones, Robert A. Holt posted to short-reads software by nmohelli on 2008-05-13 17:14:39 as along with 14 people n00c katholt jbhiatt jsatkosk AaronDarling floatingpoint idoerg caseybrown druvus natstreet azazello iris42 Neeperando yoonk
	High-throughput sequence alignment using Graphics Processing Units [My Copy] BMC Bioinformatics, Vol. 8, No. 1. (2007) by Michael Schatz, Cole Trapnell, Arthur Delcher, Amitabh Varshney posted to alignment file-import-08-05-13 gpu high_throughput mummer sequence short-reads software technologies by nmohelli on 2008-05-13 16:14:13 as
	The impact of next-generation sequencing technology on genetics [My Copy] Trends in Genetics, Vol. In Press, Corrected Proof by Elaine R. Mardis posted to file-import-08-05-13 short-reads by nmohelli on 2008-05-13 16:14:12 as
	Bioinformatics challenges of new sequencing technology [My Copy] Trends in Genetics, Vol. In Press, Corrected Proof by Mihai Pop, Steven L. Salzberg posted to 454 file-import-08-05-13 resequencing short-reads solexa solid by nmohelli on 2008-05-13 16:14:12 as
	PET-Tool: a software suite for comprehensive processing and managing of Paired-End diTag (PET) sequence data [My Copy] BMC Bioinformatics, Vol. 7 (August 2006), 390. by Kuo P. Chiu, Chee H. Wong, Qiongyu Chen, et al.Pramila Ariyaratne, Hong S. Ooi, Chia L. Wei, Wing, Yijun Ruan posted to alignment file-import-08-05-13 mapping short-reads software by nmohelli on 2008-05-13 16:14:12 as
	Comparative genome assembly. [My Copy] Brief Bioinform, Vol. 5, No. 3. (September 2004), pp. 237-248. by M. Pop, A. Phillippy, A. L. Delcher, S. L. Salzberg posted to amos comparative_genomic file-import-08-05-13 short-reads software by nmohelli on 2008-05-13 16:14:12 as
	SOAP: short oligonucleotide alignment program. [My Copy] Bioinformatics (January 2008) by Ruiqiang Li, Yingrui Li, Karsten Kristiansen, Jun Wang posted to file-import-08-05-13 short-reads by nmohelli on 2008-05-13 16:14:12 as
	R-Coffee: a method for multiple alignment of non-coding RNA. [My Copy] Nucleic acids research (April 2008) by Andreas Wilm, Desmond G. G. Higgins, Cédric Notredame posted to file-import-08-05-13 short-reads by nmohelli on 2008-05-13 16:14:12 as

Note: You may cite this page as: http://www.citeulike.org/user/nmohelli

short-reads	14
software	7
file-import-08-05-13	7
assembly	3
snp	2
assembling	2
alignment	2
haplotype	1
clustering	1
454	1
solid	1
inference	1
gpu	1
amos	1
solexa	1
soft	1
mummer	1
qpalma	1
high_throughput	1
est	1
mapping	1
resequencing	1
sequence	1
comparative_genomic	1
technologies	1

nmohelli's library 17 articles Export

nmohelli's tags