Kmer-SSR
Kmer-SSR detects simple sequence repeats (SSRs, microsatellites) in genomic nucleotide sequences, providing exhaustive identification with complete precision and recall for applications in population genetics, phylogenetics, and forensics.
Key Features:
- Exhaustive Detection: Provides an exhaustive detection mode that identifies all SSRs of specified lengths with reported 100% precision and recall.
- Parallelized Processing: Leverages parallel computing to increase processing speed for large genomic datasets while maintaining exhaustive detection.
- Flexible Filtering Options: Includes filtering options to select subsets of SSRs based on customizable criteria.
Scientific Applications:
- Population Genetics: Enables analysis of SSR variation to assess genetic diversity and evolutionary relationships within and between species.
- Phylogenetics: Aids construction of phylogenetic trees and inference of evolutionary histories using precise SSR identification.
- Forensics: Facilitates DNA profiling and individual identification via accurate SSR detection.
Methodology:
Uses an exhaustive detection mode and a parallelized approach to comprehensively scan genomic sequences, with algorithmic design prioritizing both speed and accuracy.
Topics
Details
- Tool Type:
- command-line tool
- Operating Systems:
- Linux
- Programming Languages:
- C++
- Added:
- 6/18/2018
- Last Updated:
- 11/25/2024
Operations
Publications
Pickett BD, Miller JB, Ridge PG. Kmer-SSR: a fast and exhaustive SSR search algorithm. Bioinformatics. 2017;33(24):3922-3928. doi:10.1093/bioinformatics/btx538. PMID:28968741. PMCID:PMC5860095.