Evidence map›Paper›PMID 37843103›Full record

ArticleNucleic acids research2024

OrthoMaM v12: a database of curated single-copy ortholog alignments and trees to study mammalian evolutionary genomics.

Rémi Allio, Frédéric Delsuc, Khalid Belkhir, Emmanuel J P Douzery, Vincent Ranwez, Céline Scornavacca

Abstract read
In one paragraph

Article in Nucleic acids research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

19 citing papers in PubMed.

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  7. Indirect genomic effects shape cancer risk across species.bioRxiv : the preprint server for biology · 2026
    Article
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  16. Linking phenotype to genotype using comprehensive genomic comparisons.Current opinion in genetics & development · 2025
    Review
  17. Article
  18. Article
  19. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Rémi AllioCBGP, INRAE, CIRAD, IRD, Institut Agro, Univ. Montpellier, Montpellier, 34988, France.ORCID 0000-0003-3885-5410
Frédéric DelsucISEM, Univ. Montpellier, CNRS, IRD, Montpellier, 34095, France.ORCID 0000-0002-6501-6287
Khalid BelkhirISEM, Univ. Montpellier, CNRS, IRD, Montpellier, 34095, France.ORCID 0000-0003-2768-7722
Emmanuel J P DouzeryISEM, Univ. Montpellier, CNRS, IRD, Montpellier, 34095, France.ORCID 0000-0001-5286-647X
Vincent RanwezAGAP, Univ. Montpellier, CIRAD, INRAE, Institut Agro, Montpellier, 34398, France.ORCID 0000-0002-9308-7541
Céline ScornavaccaISEM, Univ. Montpellier, CNRS, IRD, Montpellier, 34095, France.ORCID 0009-0004-0179-9771

Funding

European Research Council ERC-2015-CoG-683257
6 · The paper itself

Abstract

To date, the databases built to gather information on gene orthology do not provide end-users with descriptors of the molecular evolution information and phylogenetic pattern of these orthologues. In this context, we developed OrthoMaM, a database of ORTHOlogous MAmmalian Markers describing the evolutionary dynamics of coding sequences in mammalian genomes. OrthoMaM version 12 includes 15,868 alignments of orthologous coding sequences (CDS) from the 190 complete mammalian genomes currently available. All annotations and 1-to-1 orthology assignments are based on NCBI. Orthologous CDS can be mined for potential informative markers at the different taxonomic levels of the mammalian tree. To this end, several evolutionary descriptors of DNA sequences are provided for querying purposes (e.g. base composition and relative substitution rate). The graphical web interface allows the user to easily browse and sort the results of combined queries. The corresponding multiple sequence alignments and ML trees, inferred using state-of-the art approaches, are available for download both at the nucleotide and amino acid levels. OrthoMaM v12 can be used by researchers interested either in reconstructing the phylogenetic relationships of mammalian taxa or in understanding the evolutionary dynamics of coding sequences in their genomes. OrthoMaM is available for browsing, querying and complete or filtered download at https://orthomam.mbb.cnrs.fr/.

Indexed as

Databases, GeneticGenomicsAnimalsBase SequenceBiological EvolutionGenomeMammalsPhylogeny

Identifiers

PMID37843103
PMCPMC10767847

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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.