Evidence map›Paper›PMID 42465388›Full record

ArticlebioRxiv : the preprint server for biology2026

MKMC enables reference-free transcriptomic analysis using k-mer representations.

Lajoyce Mboning, Maciej Długosz, Marek Kokot, Jingxun Chen, Emma K Costa, Man-Ru Wu, Sui Wang, Louis-S Bouchard, Sebastian Deorowicz, Matteo Pellegrini

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. 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
–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

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

10 authors.

Lajoyce MboningDepartment of Chemistry and Biochemistry, University of California, Los Angeles, California, USA.ORCID 0009-0004-5047-5351
Maciej DługoszDepartment of Algorithmics and Software, Silesian University of Technology, Gliwice, Poland.ORCID 0000-0001-5986-4979
Marek KokotDepartment of Algorithmics and Software, Silesian University of Technology, Gliwice, Poland.ORCID 0000-0002-6420-1587
Jingxun ChenDepartment of Genetics, Stanford University, School of Medicine, California, United States.ORCID 0000-0001-7320-8652
Emma K CostaDepartment of Neurology and Neurological Sciences, Stanford University, California, United States.ORCID 0000-0002-9431-6852
Man-Ru WuDepartment of Ophthalmology, Mary M. and Sash A. Spencer Center for Vision Research, Byers Eye Institute, Stanford University, California, USA.
Sui WangDepartment of Ophthalmology, Mary M. and Sash A. Spencer Center for Vision Research, Byers Eye Institute, Stanford University, California, USA.ORCID 0000-0003-1563-9117
Louis-S BouchardDepartment of Chemistry and Biochemistry, University of California, Los Angeles, California, USA.ORCID 0000-0003-4151-5628
Sebastian DeorowiczDepartment of Algorithmics and Software, Silesian University of Technology, Gliwice, Poland.ORCID 0000-0002-9496-733X
Matteo PellegriniDepartment of Molecular, Cell and Developmental Biology, University of California Los Angeles, California, USA.ORCID 0000-0001-9355-9564

Funding

Training Program in Basic NeuroscienceT32MH020016 · NIMH · STANFORD UNIVERSITY · PI Justin L Gardner, Merritt C Maduke · 1997 to 2026
$16.2M
Training Grant in Genomic Analysis and InterpretationT32HG002536 · NHGRI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Valerie A Arboleda, Harold Pimentel · 2002 to 2026
$8.6M
Stanford Vision Research CoreP30EY026877 · NEI · STANFORD UNIVERSITY · PI Jeffrey L Goldberg · 2017 to 2026
$8.0M
NEI NIH HHS P30 EY026877NHGRI NIH HHS T32 HG002536NIMH NIH HHS T32 MH020016
6 · The paper itself

Abstract

Traditional RNA-seq analysis depends heavily on genome alignment and gene annotation, limiting its utility in non-model organisms and introducing biases that can obscure regulatory complexity. We present MKMC (Multi-sample Kmer Counter), a scalable, reference-free toolkit for RNA-seq analysis that leverages k-mer-based statistics to detect biological variation without requiring alignment. MKMC integrates fast k-mer counting, abundance matrix generation, normalization, dimensionality reduction, and differential analysis into a unified workflow. Across diverse datasets, MKMC recapitulates key biological signals-including sex differences in killifish liver-and matches alignment-based pipelines in differential expression analysis and transcriptomic age prediction. Notably, MKMC detects isoform-specific events missed by traditional methods, one of which we validated using in situ hybridization. These results reveal previously hidden isoform-level regulatory events that contribute to sex- and age-associated transcriptional programs. MKMC offers a robust, extensible alternative to alignment-based approaches, enabling transcriptomic discovery across both model and non-model systems. While we focus here on RNA-seq as a primary application, MKMC is broadly applicable to any k-mer-based analysis of next-generation sequencing data.

Indexed as

k-mersMKMCnon-model organismsRNA-seq toolkittranscriptomic age prediction

Identifiers

PMID42465388
PMCPMC13370388

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.