Difference between revisions of "SNAP"
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| − | [[Category:Software]][[Category:biology | + | [[Category:Software]][[Category:biology]][[Category:sequencing]] |
{|<!--CONFIGURATION: REQUIRED--> | {|<!--CONFIGURATION: REQUIRED--> | ||
|{{#vardefine:app|snap}} | |{{#vardefine:app|snap}} | ||
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* HPC_{{uc:{{#var:app}}}}_DIR - installation directory | * HPC_{{uc:{{#var:app}}}}_DIR - installation directory | ||
* HPC_{{uc:{{#var:app}}}}_BIN - executable directory | * HPC_{{uc:{{#var:app}}}}_BIN - executable directory | ||
| + | * HPC_SNAP_DOC - documentation directory | ||
<!--Configuration--> | <!--Configuration--> | ||
{{#if: {{#var: conf}}|==Configuration== | {{#if: {{#var: conf}}|==Configuration== | ||
Latest revision as of 20:42, 12 August 2022
Description
SNAP is a program that is part of a gene sequencing pipeline. It takes data from gene sequencing hardware that consists of short chunks of DNA (typically 70-300 base pairs long) called reads and determines where, how well and how unambiguously they match to a given reference genome. This is a computationally challenging problem because reference genomes are big (the human genome is over 3 billion base pairs long) and are often highly repetitive.
Environment Modules
Run module spider snap to find out what environment modules are available for this application.
System Variables
- HPC_SNAP_DIR - installation directory
- HPC_SNAP_BIN - executable directory
- HPC_SNAP_DOC - documentation directory
Citation
If you publish research that uses snap you have to cite it as follows: