Evidence map›Paper›PMID 39230701›Full record

ArticleBioinformatics (Oxford, England)2024

Metagenomic functional profiling: to sketch or not to sketch?

Mahmudur Rahman Hera, Shaopeng Liu, Wei Wei, Judith S Rodriguez, Chunyu Ma, David Koslicki

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Trial
  2. Estimation of substitution and indel rates via k-mer statistics.Algorithms for molecular biology : AMB · 2026
    Article
  3. Article
  4. The gift of novelty: repeat-robustbioRxiv : the preprint server for biology · 2026
    Article
  5. Review
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  13. Estimation of substitution and indel rates viaAlgorithms in bioinformatics : ... International Workshop, WABI ..., proceedings. WABI (Workshop) · 2025
    Article
  14. Estimation of substitution and indel rates viabioRxiv : the preprint server for biology · 2025
    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.

Mahmudur Rahman HeraSchool of Electrical Engineering and Computer Science, Pennsylvania State University, University Park, Pennsylvania 16802, United States.
Shaopeng LiuBioinformatics and Genomics, Huck Institutes of the Life Sciences, Pennsylvania State University, University Park, Pennsylvania 16802, United States.
Wei WeiBioinformatics and Genomics, Huck Institutes of the Life Sciences, Pennsylvania State University, University Park, Pennsylvania 16802, United States.
Judith S RodriguezBioinformatics and Genomics, Huck Institutes of the Life Sciences, Pennsylvania State University, University Park, Pennsylvania 16802, United States.
Chunyu MaBioinformatics and Genomics, Huck Institutes of the Life Sciences, Pennsylvania State University, University Park, Pennsylvania 16802, United States.
David KoslickiSchool of Electrical Engineering and Computer Science, Pennsylvania State University, University Park, Pennsylvania 16802, United States.

Funding

Leveraging k-mer sketching statistics to enhance metagenomic methods and alignment algorithmsR01GM146462 · NIGMS · PENNSYLVANIA STATE UNIVERSITY, THE · PI Antonio Blanca Pimentel, David Koslicki · 2022 to 2026
$2.2M
NIGMS NIH HHS R01 GM146462NIH HHS R01GM146462
6 · The paper itself

Abstract

motivationFunctional profiling of metagenomic samples is essential to decipher the functional capabilities of microbial communities. Traditional and more widely used functional profilers in the context of metagenomics rely on aligning reads against a known reference database. However, aligning sequencing reads against a large and fast-growing database is computationally expensive. In general, k-mer-based sketching techniques have been successfully used in metagenomics to address this bottleneck, notably in taxonomic profiling. In this work, we describe leveraging FracMinHash (implemented in sourmash, a publicly available software), a k-mer-sketching algorithm, to obtain functional profiles of metagenome samples.

resultsWe show how pieces of the sourmash software (and the resulting FracMinHash sketches) can be put together in a pipeline to functionally profile a metagenomic sample. We named our pipeline fmh-funprofiler. We report that the functional profiles obtained using this pipeline demonstrate comparable completeness and better purity compared to the profiles obtained using other alignment-based methods when applied to simulated metagenomic data. We also report that fmh-funprofiler is 39-99× faster in wall-clock time, and consumes up to 40-55× less memory. Coupled with the KEGG database, this method not only replicates fundamental biological insights but also highlights novel signals from the Human Microbiome Project datasets. AVAILABILITY AND IMPLEMENTATION: This fast and lightweight metagenomic functional profiler is freely available and can be accessed here: https://github.com/KoslickiLab/fmh-funprofiler. All scripts of the analyses we present in this manuscript can be found on GitHub.

Indexed as

AlgorithmsMetagenomeMetagenomicsSoftwareDatabases, GeneticHumansMicrobiota

Identifiers

PMID39230701
PMCPMC11373326

What OpenQuestion holds

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LicenceCC BY
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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.