Evidence map›Paper›PMID 41584516›Full record

ArticleFrontiers in bioinformatics2025

Assessment of phylogenetic informativeness in mitochondrial and nuclear genes for mammalian systematics using sparse learning.

Carlos G Schrago, Beatriz Mello

Abstract read
In one paragraph

Article in Frontiers in bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Carlos G SchragoDepartment of Genetics, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Beatriz MelloDepartment of Genetics, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the growing availability of nuclear genomic data, mitochondrial genes remain the most widely used molecular markers in mammalian systematics. However, a quantitative assessment of the phylogenetic information content of mitochondrial loci compared to nuclear loci has never been carried out. Here, we apply a sparse learning approach based on Lasso regression to evaluate the contribution of alignment sites to phylogenetic likelihoods, providing the first estimates of phylogenetically effective lengths for markers commonly used in mammalian systematics. Analyzing more than 30,000 complete mammalian mitochondrial genomes and nuclear panels composed of either 100 randomly selected complete coding sequences or of partial gene segments from conventional markers, we examined phylogenetic informativeness at two taxonomic levels: within-species and among-species. On average, ∼32% of mitochondrial sites and ∼38% of nuclear sites were classified as phylogenetically informative. We found that the number of phylogenetically informative sites were positively correlated with total gene length. Therefore, longer mitochondrial genes, particularly

Indexed as

Lasso regressionmitochondrial genomemolecular taxonomyphylogenetic informativenessphylogenetic signalsparse learningspecies delimitation

Identifiers

PMID41584516
PMCPMC12824000

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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.