Imputation of ancient genomes
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O. Delaneau | Anna-Sapfo Malaspinas | M. Sikora | E. Willerslev | H. Schroeder | M. Allentoft | N. Johannsen | A. Szczepanek | P. Włodarczak | M. Przybyła | S. Rubinacci | M. Szmyt | Bárbara Sousa da Mota | D. C. Cruz Dávalos | Carlos Eduardo G. Amorim | C. E. G. Amorim
[1] Domingo C. Salazar-García,et al. Population Genomics of Stone Age Eurasia , 2022, bioRxiv.
[2] Mattias Jakobsson,et al. An empirical evaluation of genotype imputation of ancient DNA , 2021, bioRxiv.
[3] J. Novembre,et al. Parental relatedness through time revealed by runs of homozygosity in ancient DNA , 2021, Nature Communications.
[4] B. Browning,et al. Fast two-stage phasing of large-scale sequence data. , 2021, American journal of human genetics.
[5] F. Montinaro,et al. Ancient genomes reveal structural shifts after the arrival of Steppe-related ancestry in the Italian Peninsula , 2021, Current Biology.
[6] O. Delaneau,et al. The genomic history of the Aegean palatial civilizations , 2021, Cell.
[7] S. Myers,et al. Rapid genotype imputation from sequence with reference panels , 2021, Nature Genetics.
[8] C. Ruff,et al. Predicting skeletal stature using ancient DNA , 2021, bioRxiv.
[9] T. Kivisild,et al. Evaluating genotype imputation pipeline for ultra-low coverage ancient genomes , 2020, Scientific Reports.
[10] C. Tyler-Smith,et al. A Genetic History of the Near East from an aDNA Time Course Sampling Eight Points in the Past 4,000 Years , 2020, American journal of human genetics.
[11] S. Rubinacci,et al. Efficient phasing and imputation of low-coverage sequencing data using large reference panels , 2020, bioRxiv.
[12] Swapan Mallick,et al. Insights into human genetic variation and population history from 929 diverse genomes , 2019, Science.
[13] Matthew R. Robinson,et al. Accurate, scalable and integrative haplotype estimation , 2019, Nature Communications.
[14] Torsten Günther and Mattias Jakobsson. Population Genomic Analyses of DNA from Ancient Remains , 2019, Handbook of Statistical Genomics.
[15] Joseph K. Pickrell,et al. Comparing low-pass sequencing and genotyping for trait mapping in pharmacogenetics , 2019, bioRxiv.
[16] S. Rasmussen,et al. Unraveling ancestry, kinship, and violence in a Late Neolithic mass grave , 2019, Proceedings of the National Academy of Sciences.
[17] Brian E. Cade,et al. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program , 2019, Nature.
[18] Yun S. Song,et al. Early human dispersals within the Americas , 2018, Science.
[19] T. Günther,et al. The presence and impact of reference bias on population genomic studies of prehistoric human populations , 2018, bioRxiv.
[20] P. Donnelly,et al. The UK Biobank resource with deep phenotyping and genomic data , 2018, Nature.
[21] Brian L Browning,et al. Genotype Imputation from Large Reference Panels. , 2018, Annual review of genomics and human genetics.
[22] Peter K. Joshi,et al. Runs of homozygosity: windows into population history and trait architecture , 2018, Nature Reviews Genetics.
[23] Mattias Jakobsson,et al. Southern African ancient genomes estimate modern human divergence to 350,000 to 260,000 years ago , 2017, Science.
[24] L. Excoffier,et al. Ancient genomes show social and reproductive behavior of early Upper Paleolithic foragers , 2017, Science.
[25] R. McLaughlin,et al. The population genomics of archaeological transition in west Iberia: Investigation of ancient substructure using imputation and haplotype-based methods , 2017, bioRxiv.
[26] Daniel Wegmann,et al. ATLAS: Analysis Tools for Low-depth and Ancient Samples , 2017, bioRxiv.
[27] Brian L Browning,et al. Genotype Imputation with Millions of Reference Samples. , 2016, American journal of human genetics.
[28] James Mallory,et al. Neolithic and Bronze Age migration to Ireland and establishment of the insular Atlantic genome , 2015, Proceedings of the National Academy of Sciences.
[29] Gabor T. Marth,et al. A global reference for human genetic variation , 2015, Nature.
[30] Swapan Mallick,et al. An early modern human from Romania with a recent Neanderthal ancestor , 2015, Nature.
[31] Heng Li,et al. Genome sequence of a 45,000-year-old modern human from western Siberia , 2014, Nature.
[32] Bonnie Berger,et al. Ancient human genomes suggest three ancestral populations for present-day Europeans , 2013, Nature.
[33] O. Delaneau,et al. Supplementary Information for ‘ Improved whole chromosome phasing for disease and population genetic studies ’ , 2012 .
[34] Swapan Mallick,et al. Ancient Admixture in Human History , 2012, Genetics.
[35] B. Shapiro,et al. Ancient DNA , 2020, Definitions.
[36] B. Browning,et al. Haplotype phasing: existing methods and new developments , 2011, Nature Reviews Genetics.
[37] A. Siepel,et al. Bayesian inference of ancient human demography from individual genome sequences , 2011, Nature Genetics.
[38] Sharon R Grossman,et al. Integrating common and rare genetic variation in diverse human populations , 2010, Nature.
[39] J. Marchini,et al. Genotype imputation for genome-wide association studies , 2010, Nature Reviews Genetics.
[40] David H. Alexander,et al. Fast model-based estimation of ancestry in unrelated individuals. , 2009, Genome research.
[41] Gonçalo R. Abecasis,et al. The Sequence Alignment/Map format and SAMtools , 2009, Bioinform..
[42] P. Donnelly,et al. A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies , 2009, PLoS genetics.
[43] B. Browning,et al. Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering. , 2007, American journal of human genetics.
[44] Philip L. F. Johnson,et al. Patterns of damage in genomic DNA sequences from a Neandertal , 2007, Proceedings of the National Academy of Sciences.
[45] Manuel A. R. Ferreira,et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. , 2007, American journal of human genetics.
[46] Zhaohui S. Qin,et al. A comparison of phasing algorithms for trios and unrelated individuals. , 2006, American journal of human genetics.
[47] Terrence S. Furey,et al. The UCSC Table Browser data retrieval tool , 2004, Nucleic Acids Res..
[48] M. Przeworski. Faculty Opinions recommendation of Modeling linkage disequilibrium and identifying recombination hotspots using single-nucleotide polymorphism data. , 2003 .
[49] M. Stephens,et al. Modeling linkage disequilibrium and identifying recombination hotspots using single-nucleotide polymorphism data. , 2003, Genetics.