Difference between revisions of "MIA"
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Moskalenko (talk | contribs) (Created page with "Category:SoftwareCategory:BioinformaticsCategory:NGS {|<!--CONFIGURATION: REQUIRED--> |{{#vardefine:app|mia}} |{{#vardefine:url|https://github.com/udo-stenzel/mapp...") |
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Revision as of 17:52, 5 April 2018
Description
The basic idea of this program is to align DNA sequencing fragments (shotgun or targeted resequencing) to a reference, then call a consensus. Then the consensus is used as new reference and the process is repeated until convergence. Since it was originally designed to be used on ancient DNA, it supports a position specific substitution matrix, which improves both alignment and consensus calling on chemically damaged aDNA.
MIA has been used to assemble a number of Neandertal and early modern human mitochondria. Occasionally it has been used on smallish nuclear regions, but it will probably not scale to a genome wide analysis.
Required Modules
Serial
- mia
System Variables
- HPC_{{#uppercase:mia}}_DIR - installation directory
- HPC_{{#uppercase:mia}}_BIN - executable directory
- HPC_{{#uppercase:mia}}_MAT - matrix directory
Validation
- Validated 4/5/2018