Difference between revisions of "Hapsembler"
Moskalenko (talk | contribs) |
|||
Line 79: | Line 79: | ||
<!--Turn the Table of Contents and Edit paragraph links ON/OFF--> | <!--Turn the Table of Contents and Edit paragraph links ON/OFF--> | ||
__NOTOC____NOEDITSECTION__ | __NOTOC____NOEDITSECTION__ | ||
+ | =Validation= | ||
+ | * Validated 4/5/2018 |
Revision as of 19:07, 5 April 2018
Description
Hapsembler is a haplotype-specific genome assembly toolkit that is designed for genomes that are rich in SNPs and other types of polymorphism. Hapsembler can be used to assemble reads from a variety of platforms including Illumina and Roche/454.
The Hapsembler pipeline is described in contain three main stages:
- error correction
- genome assembly
- scaffolding
Required Modules
System Variables
- HPC_{{#uppercase:hapsembler}}_DIR
Citation
If you publish research that uses hapsembler you have to cite it as follows:
To cite Hapsembler and Encore:
Nilgun Donmez and Michael Brudno (2011) Hapsembler: an assembler for highly polymorphic genomes. In Proceedings of the 15th Annual international conference on Research in computational molecular biology (RECOMB'11), Springer-Verlag, Berlin, Heidelberg, 38-52.
To cite Scarpa:
Nilgun Donmez and Michael Brudno (2013) Scarpa: Scaffolding reads with practical algorithms, Bioinformatics, 29 (2013), 428-434
Validation
- Validated 4/5/2018