MétaCan
Menu
Back to cohort
Record W2124429242 · doi:10.1126/science.aab3761

Global diversity, population stratification, and selection of human copy-number variation

2015· article· en· W2124429242 on OpenAlexaff
Peter H. Sudmant, Swapan Mallick, Bradley J. Nelson, Fereydoun Hormozdiari, Niklas Krumm, John Huddleston, Bradley P. Coe, Carl Baker, Susanne Nordenfelt, Michael J. Bamshad, Lynn B. Jorde, Olga L. Posukh, Hovhannes Sahakyan, W. Scott Watkins, Levon Yepiskoposyan, Muhammad Syafiq Abdullah, Cláudio M. Bravi, Cristian Capelli, Tor Hervig, Joseph Wee, Chris Tyler‐Smith, George van Driem, Irene Gallego Romero, Aashish R. Jha, Sena Karachanak-Yankova, Драга Тончева, David Comas, Brenna M. Henn, Toomas Kivisild, Andrés Ruiz‐Linares, Antti Sajantila, Ene Metspalu, Jüri Parik, Richard Villems, Elena B. Starikovskaya, George Ayodo, Cynthia M. Beall, Anna Di Rienzo, Michael F. Hammer, Р. И. Хусаинова, Э. К. Хуснутдинова, William Klitz, Cheryl A. Winkler, Damian Labuda, Mait Metspalu, Sarah A. Tishkoff, Stanislav Dryomov, R. I. Sukernik, Nick Patterson, David Reich, Evan E. Eichler

Bibliographic record

VenueScience · 2015
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicGenomic variations and chromosomal abnormalities
Canadian institutionsCentre Hospitalier Universitaire Sainte-Justine
FundersH2020 European Research CouncilNational Institute of Diabetes and Digestive and Kidney DiseasesNational Institute of General Medical SciencesNational Cancer InstituteNational Heart, Lung, and Blood InstituteNational Center for Chronic Disease Prevention and Health PromotionCenter for Cancer ResearchMinistry of Education and Science of the Russian FederationNational Science FoundationWellcomePaul G. Allen Family FoundationNational Institute of Environmental Health SciencesSimons FoundationNational Institutes of HealthU.S. Public Health ServiceHoward Hughes Medical InstituteNational Human Genome Research InstituteWellcome Trust
KeywordsBiologyCopy-number variationEvolutionary biologyGenomeHuman genomeLineage (genetic)Segmental duplicationStructural variationVariation (astronomy)PopulationGeneticsSelection (genetic algorithm)Gene duplicationHuman genetic variationGeneGene family

Abstract

fetched live from OpenAlex

In order to explore the diversity and selective signatures of duplication and deletion human copy-number variants (CNVs), we sequenced 236 individuals from 125 distinct human populations. We observed that duplications exhibit fundamentally different population genetic and selective signatures than deletions and are more likely to be stratified between human populations. Through reconstruction of the ancestral human genome, we identify megabases of DNA lost in different human lineages and pinpoint large duplications that introgressed from the extinct Denisova lineage now found at high frequency exclusively in Oceanic populations. We find that the proportion of CNV base pairs to single-nucleotide-variant base pairs is greater among non-Africans than it is among African populations, but we conclude that this difference is likely due to unique aspects of non-African population history as opposed to differences in CNV load.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.001
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.001
Threshold uncertainty score0.004

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.001
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.001
Science and technology studies0.0000.001
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0010.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.017
GPT teacher head0.270
Teacher spread0.253 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations378
Published2015
Admission routes1
Has abstractyes

Explore more

Same venueScienceSame topicGenomic variations and chromosomal abnormalitiesFrench-language works237,207