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archive:bioinformatic_tools:sharcgs [2010/04/09 12:10]
cbrumbau
archive:bioinformatic_tools:sharcgs [2015/07/28 06:26] (current)
ceisenhart ↷ Page moved from bioinformatic_tools:sharcgs to archive:bioinformatic_tools:sharcgs
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 SHARCGS is a //de novo// DNA assembly program that uses 25-40mers and deep sequence coverage to assemble genomes. SHARCGS is a //de novo// DNA assembly program that uses 25-40mers and deep sequence coverage to assemble genomes.
 +It was used for //de novo// sequencing from Solexa sequencing data of //​Helicobacter acinonychis//​[(cite:​SHARCGSHaci>​Juliane C. Dohm, Claudio Lottaz, Tatiana Borodina, and Heinz Himmelbauer. Substantial biases in ultra-short read data sets from high-throughput DNA sequencing. //Nucleic Acids Research// Advance Access published on July 26, 2008, doi:​[[http://​dx.doi.org/​10.1093/​nar/​gkn425|10.1093/​nar/​gkn425]])].
  
 ==== Website ==== ==== Website ====
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 [[http://​sharcgs.molgen.mpg.de/​download.shtml]] [[http://​sharcgs.molgen.mpg.de/​download.shtml]]
  
-===== Publications ===== 
-SHARCGS deployed in a following paper when used for //de novo// sequencing from Solexa sequencing data of //​Helicobacter acinonychis//:​ 
  
-Juliane C. Dohm , Claudio Lottaz , Tatiana Borodina , and Heinz Himmelbauer. Substantial biases in ultra-short read data sets from high-throughput DNA sequencing. //Nucleic Acids Research// Advance Access published on July 26, 2008, doi:​[[http://​dx.doi.org/​10.1093/​nar/​gkn425|10.1093/​nar/​gkn425]]. 
  
 ===== References ===== ===== References =====
 <​refnotes>​notes-separator:​ none</​refnotes>​ <​refnotes>​notes-separator:​ none</​refnotes>​
 ~~REFNOTES cite~~ ~~REFNOTES cite~~
archive/bioinformatic_tools/sharcgs.1270815054.txt.gz · Last modified: 2010/04/09 12:10 by cbrumbau