SMC++
SMC++ estimates historical population size changes and population split times from whole-genome sequence data to infer past demographic events without requiring phased genomes.
Key Features:
- Genealogical inference with recombination: Leverages genealogical processes with recombination to infer demographic history from sequence data.
- Unphased data compatibility: Performs inference on unphased whole-genome sequence data, avoiding phasing switch errors.
- Scalability: Handles substantially larger sample sizes to increase resolution in recent historical periods.
- Joint inference of sizes and splits: Jointly infers population size histories and split times among diverged populations.
- Spline regularization: Employs a spline regularization scheme that reduces estimation error in demographic reconstructions.
Scientific Applications:
- Human population genomics: Applied to sequence data from over a thousand human genomes spanning Africa and Eurasia to infer human demographic history.
- Drosophila population genomics: Applied to hundreds of Drosophila melanogaster genomes from an African population.
- Avian population genomics: Applied to tens of zebra finch and long-tailed finch genomes from Australian populations.
- Cross-species demographic inference: Demonstrated versatility across diverse species' genomic datasets for reconstructing population history.
Methodology:
Performs inference using genealogical processes incorporating recombination on whole-genome sequences, operates on unphased data, jointly estimates population size histories and split times, and applies spline regularization to reduce estimation error while scaling to large sample sizes.
Topics
Details
- License:
- GPL-3.0
- Cost:
- Free of charge
- Tool Type:
- command-line tool
- Operating Systems:
- Linux, Mac
- Programming Languages:
- Python, C++
- Added:
- 3/18/2022
- Last Updated:
- 3/21/2022
Operations
Publications
Terhorst J, Kamm JA, Song YS. Robust and scalable inference of population history from hundreds of unphased whole genomes. Nature Genetics. 2016;49(2):303-309. doi:10.1038/ng.3748. PMID:28024154. PMCID:PMC5470542.