Evidence map›Paper›PMID 38166646›Full record

ArticleBMC genomic data2024

Dating ancient splits in phylogenetic trees, with application to the human-Neanderthal split.

Keren Levinstein Hallak, Saharon Rosset

Open access · goldAbstract read
In one paragraph

Article in BMC genomic data, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 48% of its field
1 · What the graph read from it

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.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Keren Levinstein HallakDepartment of Statistics and Operations Research, School of Mathematical Sciences, Tel-Aviv University, Tel-Aviv, 6997801, Israel.
Saharon RossetDepartment of Statistics and Operations Research, School of Mathematical Sciences, Tel-Aviv University, Tel-Aviv, 6997801, Israel. saharon@tauex.tau.ac.il.
Tel Aviv University · IL

Funding

Israeli Science Foundation grant 2180/20
6 · The paper itself

Abstract

backgroundWe tackle the problem of estimating species TMRCAs (Time to Most Recent Common Ancestor), given a genome sequence from each species and a large known phylogenetic tree with a known structure (typically from one of the species). The number of transitions at each site from the first sequence to the other is assumed to be Poisson distributed, and only the parity of the number of transitions is observed. The detailed phylogenetic tree contains information about the transition rates in each site. We use this formulation to develop and analyze multiple estimators of the species' TMRCA. To test our methods, we use mtDNA substitution statistics from the well-established Phylotree as a baseline for data simulation such that the substitution rate per site mimics the real-world observed rates.

resultsWe evaluate our methods using simulated data and compare them to the Bayesian optimizing software BEAST2, showing that our proposed estimators are accurate for a wide range of TMRCAs and significantly outperform BEAST2. We then apply the proposed estimators on Neanderthal, Denisovan, and Chimpanzee mtDNA genomes to better estimate their TMRCA with modern humans and find that their TMRCA is substantially later, compared to values cited recently in the literature.

conclusionsOur methods utilize the transition statistics from the entire known human mtDNA phylogenetic tree (Phylotree), eliminating the requirement to reconstruct a tree encompassing the specific sequences of interest. Moreover, they demonstrate notable improvement in both running speed and accuracy compared to BEAST2, particularly for earlier TMRCAs like the human-Chimpanzee split. Our results date the human - Neanderthal TMRCA to be [Formula: see text] years ago, considerably later than values cited in other recent studies.

Indexed as

HominidaeNeanderthalsAnimalsBayes TheoremDNA, MitochondrialHumansPan troglodytesPhylogenyDNA, MitochondrialAncient humansBEAST2ChimpanzeeDenisovanDivergence timesMitochondrial DNA (mtDNA)NeanderthalPoisson parityTime to most recent common ancestor (TMRCA)Transition rates

Identifiers

PMID38166646
PMCPMC10759710
OpenAlexW4390501512

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.