ReviewNature reviews. Genetics2014
The impact of whole-genome sequencing on the reconstruction of human population history.
Review in Nature reviews. Genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
55 citing papers in PubMed.
- Large-scale single-cell phylogenetic mapping of clonal evolution in the human aging esophagus.bioRxiv : the preprint server for biology · 2025Article
- Real-World Data: Implementation and Outcomes of Next-Generation Sequencing in the MENA Region.Diagnostics (Basel, Switzerland) · 2025Article
- Review
- Genomes of extinct hominins and human reproductive evolution.EXCLI journal · 2023Article
- Population-specific causal disease effect sizes in functionally important regions impacted by selection.Nature communications · 2021Article
- Admixture-enabled selection for rapid adaptive evolution in the Americas.Genome biology · 2020Article
- Neanderthal-Denisovan ancestors interbred with a distantly related hominin.Science advances · 2020Article
- Whole-genome sequencing of 128 camels across Asia reveals origin and migration of domestic Bactrian camels.Communications biology · 2020Article
- Unlocking the origins and biology of domestic animals using ancient DNA and paleogenomics.BMC biology · 2019Review
- Humans and Chimpanzees Display Opposite Patterns of Diversity inG3 (Bethesda, Md.) · 2019Article
- Methods for Estimating Demography and Detecting Between-Locus Differences in the Effective Population Size and Mutation Rate.Molecular biology and evolution · 2019Article
- Population Structure and Implications on the Genetic Architecture of HIV-1 Phenotypes Within Southern Africa.Frontiers in genetics · 2019Review
- Genetic ancestry, admixture and health determinants in Latin America.BMC genomics · 2018Article
- Bayesian variable selection for parametric survival model with applications to cancer omics data.Human genomics · 2018Article
- Niche adaptation and viral transmission of human papillomaviruses from archaic hominins to modern humans.PLoS pathogens · 2018Article
- Article
- Understanding 6th-century barbarian social organization and migration through paleogenomics.Nature communications · 2018Article
- The State of Data in Healthcare: Path Towards Standardization.Journal of healthcare informatics research · 2018Article
- Quantitative analysis of population-scale family trees with millions of relatives.Science (New York, N.Y.) · 2018Article
- DACCOR-Detection, characterization, and reconstruction of repetitive regions in bacterial genomes.PeerJ · 2018Article
Corrections and comments
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Authors and funding
2 authors.
Funding
Abstract
Examining patterns of molecular genetic variation in both modern-day and ancient humans has proved to be a powerful approach to learn about our origins. Rapid advances in DNA sequencing technology have allowed us to characterize increasing amounts of genomic information. Although this clearly provides unprecedented power for inference, it also introduces more complexity into the way we use and interpret such data. Here, we review ongoing debates that have been influenced by improvements in our ability to sequence DNA and discuss some of the analytical challenges that need to be overcome in order to fully exploit the rich historical information that is contained in the entirety of the human genome.
Indexed as
Identifiers
24492235What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.