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.