Evidence map›Paper›PMID 37046225›Full record

ArticleBMC bioinformatics2023

nRCFV: a new, dataset-size-independent metric to quantify compositional heterogeneity in nucleotide and amino acid datasets.

James F Fleming, Torsten H Struck

Abstract read
In one paragraph

Article in BMC bioinformatics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

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3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
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  4. Revisiting the four Hexapoda classes: Protura as the sister group to all other hexapods.Proceedings of the National Academy of Sciences of the United States of America · 2024
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

2 authors.

James F FlemingUniversity of Oslo Natural History Museum, Sars' Gata 1, Oslo, Norway. j.f.fleming@nhm.uio.no.
Torsten H StruckUniversity of Oslo Natural History Museum, Sars' Gata 1, Oslo, Norway.

Funding

Norges Forskningsråd 300587
6 · The paper itself

Abstract

motivationCompositional heterogeneity-when the proportions of nucleotides and amino acids are not broadly similar across the dataset-is a cause of a great number of phylogenetic artefacts. Whilst a variety of methods can identify it post-hoc, few metrics exist to quantify compositional heterogeneity prior to the computationally intensive task of phylogenetic tree reconstruction. Here we assess the efficacy of one such existing, widely used, metric: Relative Composition Frequency Variability (RCFV), using both real and simulated data.

resultsOur results show that RCFV can be biased by sequence length, the number of taxa, and the number of possible character states within the dataset. However, we also find that missing data does not appear to have an appreciable effect on RCFV. We discuss the theory behind this, the consequences of this for the future of the usage of the RCFV value and propose a new metric, nRCFV, which accounts for these biases. Alongside this, we present a new software that calculates both RCFV and nRCFV, called nRCFV_Reader. AVAILABILITY AND IMPLEMENTATION: nRCFV has been implemented in RCFV_Reader, available at: https://github.com/JFFleming/RCFV_Reader . Both our simulation and real data are available at Datadryad: https://doi.org/10.5061/dryad.wpzgmsbpn .

Indexed as

Amino AcidsNucleotidesComputer SimulationPhylogenySoftwareAmino AcidsNucleotidesBioinformatics softwareCompositional heterogeneityPhylogenetics

Identifiers

PMID37046225
PMCPMC10099917

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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.