Evidence map›Paper›PMID 42039534›Full record

ArticlebioRxiv : the preprint server for biology2026

Phlag: Scalable detection of genomics regions with unexplained phylogenetic heterogeneity.

Ali Osman Berk Şapcı, Shayesteh Arasti, Edward L Braun, Siavash Mirarab

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. 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.

Ali Osman Berk ŞapcıORCID 0000-0003-4396-817X

Funding

Biology-aware machine learning methods for characterizing microbiome genotype and phenotypeR35GM142725 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MIR ARABBAYGI, SIAVASH · 2021 to 2025
$1.9M
NIGMS NIH HHS R35 GM142725
6 · The paper itself

Abstract

Motivation: Phylogenetic analyses of entire genomes (phylogenomics) have revealed abundant heterogeneity of evolutionary histories. While much has been done to model this heterogeneity and to infer species trees despite it, the current toolkit has a limitation. Most methods assume that gene trees across the genome differ but are all sampled from Results: To address this challenge, we define the problem of detecting what segments of the genome are inconsistent with a putative species tree, even after allowing discordance according to MSC. We model gene trees not as a set, but rather as a series (a realization of a stochastic process) along genomic positions. We propose a Hidden Markov Model (HMM) approach applied to quartet statistics measured from gene trees and tie the model to MSC using simulations. The combined use of these three ideas leads to a scalable method called Phlag. On simulated and real data, we show that Phlag can detect many cases of change in underlying evolutionary processes, including reduced recombination rates, population size changes, and admixture, all using the same algorithm. Availability and Implementation: Phlag is available at github.com/bo1929/phlag . All results and scripts can be found at github.com/bo1929/shared.phlag .

Identifiers

PMID42039534
PMCPMC13104820

What OpenQuestion holds

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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.