Unlock your biological data

?

Paired-end read elongation software tools | De novo sequencing data analysis

Next-generation sequencing technologies generate very large numbers of short reads. Even with very deep genome coverage, short read lengths cause problems in de novo assemblies. The use of paired-end libraries with a fragment size shorter than twice the read length provides an opportunity to generate much longer reads by overlapping and merging read pairs before assembling a genome.
Source text:
(Magoč and Salzberg, 2011) FLASH: fast length adjustment of short reads to improve genome assemblies. Bioinformatics.

1 - 11 of 11 results
filter_list Filters
build Technology
laptop Operating System
desktop_windows Interface
important_devices Computer Skill
copyright Restriction to use
memory Programming Language
import_contacts Journal
account_balance Funding
1 - 11 of 11 results
0 - 0 of 0 results
1 - 5 of 5 results
filter_list Filters
business_center Job seeker
Disable 1
assignment_ind Position
public Country
memory Programming Language