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Efficient Coalescent Simulation and Genealogical Analysis for Large Sample Sizes
Open accessAbstract
A central challenge in the analysis of genetic variation is to provide realistic genome simulation across millions of samples. Present day coalescent simulations do not scale well, or use approximations that fail to capture important long-range linkage properties. Analysing the results of simulations also presents a substantial challenge, as current methods to store genealogies consume a great deal of space, are slow to parse and do not take advantage of shared structure in correlated trees. We solve these problems by introducing sparse trees and coalescence records as the key units of genealogical analysis. Using these tools, exact simulation of the coalescent with recombination for chromosome-sized regions over hundreds of thousands of samples is possible, and substantially faster than present-day approximate methods. We can also analyse the results orders of magnitude more quickly than with existing methods.
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Cites
PLINK: a tool set for whole-genome association and population-based linkage analyses.
Purcell, S., Neale, B., Todd-Brown, K., Thomas, L., Ferreira, M. A. R., Bender, D., Maller, J., Sklar, P., de Bakker, P. I. W., Daly, M. J., et al. (2007) · The American Journal of Human Genetics · doi:10.1086/519795 · Cited by 34,089
A global reference for human genetic variation
The 1000 Genomes Project Consortium, authors, C., Auton, A., Abecasis, G. R., Steering committee, Altshuler, D. M., Durbin, R. M., Abecasis, G. R., Bentley, D. R., Chakravarti, A., et al. (2015) · Nature · doi:10.1038/nature15393 · Cited by 18,247
Self-citationBiopython: freely available python tools for computational molecular biology and bioinformatics
Cock, P. J. A., Antao, T., Chang, J. T., Chapman, B. A., Cox, C. J., Dalke, A., Friedberg, I., Hamelryck, T., Kauff, F., Wilczynski, B., et al. (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp163 · Cited by 6,080
Genome-wide association studies for complex traits: consensus, uncertainty and challenges
McCarthy, M. I., Abecasis, G. R., Cardon, L. R., Goldstein, D. B., Little, J., Ioannidis, J. P. A., & Hirschhorn, J. N. (2008) · Nature Reviews Genetics · doi:10.1038/nrg2344 · Cited by 2,891
A new multipoint method for genome-wide association studies by imputation of genotypes
Marchini, J., Howie, B., Myers, S., McVean, G., & Donnelly, P. (2007) · Nature Genetics · doi:10.1038/ng2088 · Cited by 2,609
Self-citationInference of human population history from individual whole-genome sequences
Li, H., & Durbin, R. (2011) · Nature · doi:10.1038/nature10231 · Cited by 2,590
Gutenkunst, R. N., Hernandez, R. D., Williamson, S. H., & Bustamante, C. D. (2009) · PLoS Genetics · doi:10.1371/journal.pgen.1000695 · Cited by 1,906 · cited 2×
“Researchers are seeking to understand fine scale population structure using methods based on principal component analysis [112], admixture fractions [113–115], length of haplotype blocks [116–118] and allele frequencies [119].”
MethodHudson, R. R., & Kaplan, N. L. (1985) · Genetics · doi:10.1093/genetics/111.1.147 · Cited by 1,555
Genes mirror geography within Europe
Novembre, J., Johnson, T., Bryc, K., Kutalik, Z., Boyko, A. R., Auton, A., Indap, A., King, K. S., Bergmann, S., Nelson, M. R., et al. (2008) · Nature · doi:10.1038/nature07331 · Cited by 1,479
Big Data: Astronomical or Genomical?
Stephens, Z. D., Lee, S. Y., Faghri, F., Campbell, R. H., Zhai, C., Efron, M. J., Iyer, R., Schatz, M. C., Sinha, S., & Robinson, G. E. (2015) · PLOS Biology · doi:10.1371/journal.pbio.1002195 · Cited by 1,340
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Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
Taliun, D., Harris, D. N., Kessler, M. D., Carlson, J., Szpiech, Z. A., Torres, R., Taliun, S. A. G., Corvelo, A., Gogarten, S. M., Kang, H. M., et al. (2021) · Nature · doi:10.1038/s41586-021-03205-y · Cited by 2,213
Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations
Martin, A. R., Gignoux, C. R., Walters, R. K., Wojcik, G. L., Neale, B. M., Gravel, S., Daly, M. J., Bustamante, C. D., & Kenny, E. E. (2017) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2017.03.004 · Cited by 1,391
Insights into human genetic variation and population history from 929 diverse genomes
Bergström, A., McCarthy, S. A., Hui, R., Almarri, M. A., Ayub, Q., Danecek, P., Chen, Y., Felkel, S., Hallast, P., Kamm, J., et al. (2020) · Science · doi:10.1126/science.aay5012 · Cited by 1,020
Dsuite ‐ Fast D ‐statistics and related admixture evidence from VCF files
Malinsky, M., Matschiner, M., & Svardal, H. (2021) · Molecular Ecology Resources · doi:10.1111/1755-0998.13265 · Cited by 992
A method for genome-wide genealogy estimation for thousands of samples
Speidel, L., Forest, M., Shi, S., & Myers, S. R. (2019) · Nature Genetics · doi:10.1038/s41588-019-0484-x · Cited by 480
Signatures of negative selection in the genetic architecture of human complex traits
Zeng, J., de Vlaming, R., Wu, Y., Robinson, M. R., Lloyd-Jones, L. R., Yengo, L., Yap, C. X., Xue, A., Sidorenko, J., McRae, A. F., et al. (2018) · Nature Genetics · doi:10.1038/s41588-018-0101-4 · Cited by 391
Analysis of Human Sequence Data Reveals Two Pulses of Archaic Denisovan Admixture
Browning, S. R., Browning, B. L., Zhou, Y., Tucci, S., & Akey, J. M. (2018) · Cell · doi:10.1016/j.cell.2018.02.031 · Cited by 381
The population history of northeastern Siberia since the Pleistocene
Sikora, M., Pitulko, V. V., Sousa, V. C., Allentoft, M. E., Vinner, L., Rasmussen, S., Margaryan, A., de Barros Damgaard, P., de la Fuente, C., Renaud, G., et al. (2019) · Nature · doi:10.1038/s41586-019-1279-z · Cited by 389
Inferring whole-genome histories in large population datasets
Kelleher, J., Wong, Y., Wohns, A. W., Fadil, C., Albers, P. K., & McVean, G. (2019) · Nature Genetics · doi:10.1038/s41588-019-0483-y · Cited by 313
Self-citationAncient genomes show social and reproductive behavior of early Upper Paleolithic foragers
Sikora, M., Seguin-Orlando, A., Sousa, V. C., Albrechtsen, A., Korneliussen, T., Ko, A., Rasmussen, S., Dupanloup, I., Nigst, P. R., Bosch, M. D., et al. (2017) · Science · doi:10.1126/science.aao1807 · Cited by 312
Genetic diversity loss in the Anthropocene
Exposito-Alonso, M., Booker, T. R., Czech, L., Gillespie, L., Hateley, S., Kyriazis, C. C., Lang, P. L. M., Leventhal, L., Nogues-Bravo, D., Pagowski, V., et al. (2022) · Science · doi:10.1126/science.abn5642 · Cited by 288
Identifying and Interpreting Apparent Neanderthal Ancestry in African Individuals
Chen, L., Wolf, A. B., Fu, W., Li, L., & Akey, J. M. (2020) · Cell · doi:10.1016/j.cell.2020.01.012 · Cited by 254
Robinson, J. A., Brown, C., Kim, B. Y., Lohmueller, K. E., & Wayne, R. K. (2018) · Current Biology · doi:10.1016/j.cub.2018.08.066 · Cited by 221
Limits of long-term selection against Neandertal introgression
Petr, M., Pääbo, S., Kelso, J., & Vernot, B. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1814338116 · Cited by 211
Multiple episodes of interbreeding between Neanderthal and modern humans
Villanea, F. A., & Schraiber, J. G. (2018) · Nature Ecology & Evolution · doi:10.1038/s41559-018-0735-8 · Cited by 192
Ancestry-specific recent effective population size in the Americas
Browning, S. R., Browning, B. L., Daviglus, M. L., Durazo-Arvizu, R. A., Schneiderman, N., Kaplan, R. C., & Laurie, C. C. (2018) · PLOS Genetics · doi:10.1371/journal.pgen.1007385 · Cited by 187
Pendleton, A. L., Shen, F., Taravella, A. M., Emery, S., Veeramah, K. R., Boyko, A. R., & Kidd, J. M. (2018) · BMC Biology · doi:10.1186/s12915-018-0535-2 · Cited by 156
A weakly structured stem for human origins in Africa
Ragsdale, A. P., Weaver, T. D., Atkinson, E. G., Hoal, E. G., Möller, M., Henn, B. M., & Gravel, S. (2023) · Nature · doi:10.1038/s41586-023-06055-y · Cited by 159
Widespread selection and gene flow shape the genomic landscape during a radiation of monkeyflowers
Stankowski, S., Chase, M. A., Fuiten, A. M., Rodrigues, M. F., Ralph, P. L., & Streisfeld, M. A. (2019) · PLOS Biology · doi:10.1371/journal.pbio.3000391 · Cited by 134
Hubisz, M. J., Williams, A. L., & Siepel, A. (2020) · PLOS Genetics · doi:10.1371/journal.pgen.1008895 · Cited by 130
Detecting archaic introgression using an unadmixed outgroup
Skov, L., Hui, R., Shchur, V., Hobolth, A., Scally, A., Schierup, M. H., & Durbin, R. (2018) · PLoS Genetics · doi:10.1371/journal.pgen.1007641 · Cited by 125
Demographic history mediates the effect of stratification on polygenic scores
Zaidi, A. A., & Mathieson, I. (2020) · eLife · doi:10.7554/elife.61548 · Cited by 122
An ancestral recombination graph of human, Neanderthal, and Denisovan genomes
Schaefer, N. K., Shapiro, B., & Green, R. E. (2021) · Science Advances · doi:10.1126/sciadv.abc0776 · Cited by 106
“Our QC simulations were performed using msprime (59).”
MethodDetecting adaptive introgression in human evolution using convolutional neural networks
Gower, G., Picazo, P. I., Fumagalli, M., & Racimo, F. (2021) · eLife · doi:10.7554/elife.64669 · Cited by 95
Joint estimates of heterozygosity and runs of homozygosity for modern and ancient samples
Renaud, G., Hanghøj, K., Korneliussen, T. S., Willerslev, E., & Orlando, L. (2019) · Genetics · doi:10.1534/genetics.119.302057 · Cited by 101
Philippine Ayta possess the highest level of Denisovan ancestry in the world
Larena, M., McKenna, J., Sanchez-Quinto, F., Bernhardsson, C., Ebeo, C., Reyes, R., Casel, O., Huang, J.-Y., Hagada, K. P., Guilay, D., et al. (2021) · Current Biology · doi:10.1016/j.cub.2021.07.022 · Cited by 93
Model‐based detection and analysis of introgressed Neanderthal ancestry in modern humans
Steinrücken, M., Spence, J. P., Kamm, J. A., Wieczorek, E., & Song, Y. S. (2018) · Molecular Ecology · doi:10.1111/mec.14565 · Cited by 73
Haplotype-based inference of recent effective population size in modern and ancient DNA samples
Fournier, R., Tsangalidou, Z., Reich, D., & Palamara, P. F. (2023) · Nature Communications · doi:10.1038/s41467-023-43522-6 · Cited by 49
Inference of Population Structure from Time-Series Genotype Data
Joseph, T. A., & Pe’er, I. (2019) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2019.06.002 · Cited by 37
Unbiased estimation of linkage disequilibrium from unphased data
Ragsdale, A. P., & Gravel, S. (2020) · Molecular Biology and Evolution · doi:10.1093/molbev/msz265 · Cited by 36
Zhang, X., Kim, B., Lohmueller, K. E., & Huerta-Sánchez, E. (2020) · Genetics · doi:10.1534/genetics.120.303081 · Cited by 35
Guyon, L., Guez, J., Toupance, B., Heyer, E., & Chaix, R. (2024) · Nature Communications · doi:10.1038/s41467-024-47618-5 · Cited by 28
Booker, W. W., Ray, D. D., & Schrider, D. R. (2023) · GENETICS · doi:10.1093/genetics/iyad063 · Cited by 22
Taskent, O., Lin, Y. L., Patramanis, I., Pavlidis, P., & Gokcumen, O. (2020) · Genetics · doi:10.1534/genetics.120.303167 · Cited by 20
The genomic formation of First American ancestors in East and Northeast Asia
Ning, C., Fernandes, D., Changmai, P., Flegontova, O., Yüncü, E., Maier, R., Altınışık, N. E., Kassian, A. S., Krause, J., Lalueza-Fox, C., et al. (2020) · doi:10.1101/2020.10.12.336628 · Cited by 19
Ancient Rapanui genomes reveal resilience and pre-European contact with the Americas
Moreno-Mayar, J. V., Sousa da Mota, B., Higham, T., Klemm, S., Gorman Edmunds, M., Stenderup, J., Iraeta-Orbegozo, M., Laborde, V., Heyer, E., Torres Hochstetter, F., et al. (2024) · Nature · doi:10.1038/s41586-024-07881-4 · Cited by 20
Legofit: estimating population history from genetic data
Rogers, A. R. (2019) · BMC Bioinformatics · doi:10.1186/s12859-019-3154-1 · Cited by 17
Brand, C. M., White, F. J., Rogers, A. R., & Webster, T. H. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2200858119 · Cited by 10
An efficient algorithm for estimating population history from genetic data
Rogers, A. R. (2022) · Peer Community Journal · doi:10.24072/pcjournal.132 · Cited by 7
Understanding admixture fractions: theory and estimation of gene-flow
Liang, M., Shishkin, M., Shchur, V., & Nielsen, R. (2024) · Journal of Mathematical Biology · doi:10.1007/s00285-024-02146-0 · Cited by 5
The Genetic Legacy of Introgression from Two Deeply Divergent Lineages in the Genus Homo
Rogers, A. R., Islam, M. T., Brand, C. M., & Webster, T. H. (2026) · bioRxiv · doi:10.64898/2026.03.22.713509
Metadata
- Authors
- Kelleher, J., Etheridge, A. M., & McVean, G.
- Venue
- PLOS Computational Biology
- Publisher
- Public Library of Science (PLoS)
- Published
- 2016-05-04
- Volume
- 12
- Issue
- 5
- Pages
- e1004842
- ISSN
- 1553-734X (ISSN-L)
- 1553-7358
- OpenAlex
- W2951641704
- Cited by
- 654
- References
- 16
- FWCI
- 27.40
- Type
- journal article
- Language
- en
- Open access
- gold
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