Evidence map›Paper›PMID 39990503›Full record

ArticlebioRxiv : the preprint server for biology2025

A General Framework for Branch Length Estimation in Ancestral Recombination Graphs.

Yun Deng, William S DeWitt, Yun S Song, Rasmus Nielsen

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Yun DengCenter for Computational Biology, University of California, Berkeley, USA.ORCID 0000-0003-2802-2546
William S DeWittComputer Science Division, University of California, Berkeley, USA.ORCID 0000-0002-6802-9139
Yun S SongCenter for Computational Biology, University of California, Berkeley, USA.ORCID 0000-0002-0734-9868
Rasmus NielsenCenter for Computational Biology, University of California, Berkeley, USA.ORCID 0000-0003-0513-6591

Funding

Scalable Computational Methods for Genealogical Inference: from species level to single cellsR01HG013117 · NHGRI · UNIVERSITY OF CALIFORNIA BERKELEY · PI Ian H Holmes, RASMUS NIELSEN · 2024 to 2026
$1.7M
Enabling Precision Genomics Using Adaptive VariationR01GM138634 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI NIELSEN, RASMUS · 2020 to 2023
$1.7M
Inference and application of graphs for genomic dataR35GM153400 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI RASMUS NIELSEN · 2024 to 2026
$1.3M
Scalable Computational Methods for Genealogical Inference: from species level to single cellsR56HG013117 · NHGRI · UNIVERSITY OF CALIFORNIA BERKELEY · PI HOLMES, IAN H, NIELSEN, RASMUS · 2023 to 2023
$315k
NHGRI NIH HHS R01 HG013117NHGRI NIH HHS R56 HG013117NIGMS NIH HHS R01 GM138634NIGMS NIH HHS R35 GM153400
6 · The paper itself

Abstract

Inference of Ancestral Recombination Graphs (ARGs) is of central interest in the analysis of genomic variation. ARGs can be specified in terms of topologies and coalescence times. The coalescence times are usually estimated using an informative prior derived from coalescent theory, but this may generate biased estimates and can also complicate downstream inferences based on ARGs. Here we introduce, POLEGON, a novel approach for estimating branch lengths for ARGs which uses an uninformative prior. Using extensive simulations, we show that this method provides improved estimates of coalescence times and lead to more accurate inferences of effective population sizes under a wide range of demographic assumptions (population expansion, bottleneck, split, etc). It also improves other downstream inferences including estimates of mutation rates. We apply the method to data from the 1000 Genomes Project to investigate population size histories and differential mutation signatures across populations. We also estimate coalescence times in the HLA region, and show that they exceed 30 million years in multiple segments.

Indexed as

Ancestral Recombination Graphbranch length estimationuninformative prior

Identifiers

PMID39990503
PMCPMC11844452

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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.