Evidence map›Paper›PMID 39088438›Full record

ArticlePloS one2024

PC-mer: An Ultra-fast memory-efficient tool for metagenomics profiling and classification.

Saeedeh Akbari Rokn Abadi, Amirhossein Mohammadi, Somayyeh Koohi

Abstract read
In one paragraph

Article in PloS one, 2024. 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
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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

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

3 authors.

Saeedeh Akbari Rokn AbadiDepartment of Computer Engineering, Sharif University of Technology, Tehran, Iran.ORCID 0000-0001-7564-4204
Amirhossein MohammadiDepartment of Computer Engineering, Sharif University of Technology, Tehran, Iran.ORCID 0000-0002-5040-1940
Somayyeh KoohiDepartment of Computer Engineering, Sharif University of Technology, Tehran, Iran.ORCID 0000-0002-3105-2511

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Features extraction methods, such as k-mer-based methods, have recently made up a significant role in classifying and analyzing approaches for metagenomics data. But, they are challenged by various bottlenecks, such as performance limitations, high memory consumption, and computational overhead. To deal with these challenges, we developed an innovative features extraction and sequence profiling method for DNA/RNA sequences, called PC-mer, taking advantage of the physicochemical properties of nucleotides. PC-mer in comparison with the k-mer profiling methods provides a considerable memory usage reduction by a factor of 2k while improving the metagenomics classification performance, for both machine learning-based and computational-based methods, at the various levels and also archives speedup more than 1000x for the training phase. Examining ML-based PC-mer on various datasets confirms that it can achieve 100% accuracy in classifying samples at the class, order, and family levels. Despite the k-mer-based classification methods, it also improves genus-level classification accuracy by more than 14% for shotgun dataset (i.e. achieves accuracy of 97.5%) and more than 5% for amplicon dataset (i.e. achieves accuracy of 98.6%). Due to these improvements, we provide two PC-mer-based tools, which can actually replace the popular k-mer-based tools: one for classifying and another for comparing metagenomics data.

Indexed as

MetagenomicsAlgorithmsComputational BiologyHumansMachine LearningSoftware

Identifiers

PMID39088438
PMCPMC11293629

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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.