Evidence map›Paper›PMID 40085007›Full record

ArticleBioinformatics (Oxford, England)2025

bpRNA-CosMoS: a robust and efficient RNA structural comparison method using k-mer based cosine similarity.

Brittany Lasher, David A Hendrix

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

2 authors.

Brittany LasherDepartment of Biochemistry and Biophysics, Oregon State University, 2011 Agricultural and Life Sciences, 2750 SW Campus Way, Corvallis, Oregon 97331, USA.ORCID 0000-0003-2650-4162
David A HendrixDepartment of Biochemistry and Biophysics, Oregon State University, 2011 Agricultural and Life Sciences, 2750 SW Campus Way, Corvallis, Oregon 97331, USA.ORCID 0000-0002-7285-1977

Funding

Integrative transcriptomics to uncover functional elements and disease-associated variants in RNAR01GM145986 · NIGMS · OREGON STATE UNIVERSITY · PI HENDRIX, DAVID ANTHONY · 2022 to 2025
$1.2M
NIGMS NIH HHS R01 GM145986NIH HHS R01GM145986
6 · The paper itself

Abstract

motivationRNA secondary structure is often essential to function. Recent work has led to the development of high-throughput experimental probing methods for structure determination. Although structure is more conserved than primary sequence, much of the bioinformatics pipelines to connect RNA structure to function rely on nucleotide sequence alignments rather than structural similarity. There is a need to develop methods for secondary structure comparisons that are also fast and efficient to navigate the vast amounts of structural data. K-mer based similarity approaches are valued for their computational efficiency and have been applied for protein, DNA, and RNA primary sequences. However, these approaches have yet to be implemented for RNA secondary structure.

resultsOur method, bpRNA-CosMoS, fills this gap by using k-mers and length-weighted cosine similarity to compute similarity scores between RNA structures. bpRNA-CosMoS is built upon the bpRNA structure array, which represents the structural category of each nucleotide as a single-character structural code (e.g. hairpin=H, etc.). A structural comparison score is calculated through cosine similarity of the k-mer count vectors, generated from structure arrays. A major challenge with k-mer based methods is that they often ignore the length of the sequences being compared. We have overcome this with a length-weighted penalty that addresses cases of two RNAs of vastly different lengths. In addition, the use of "fuzzy counting" has added some optional flexibility to decrease the negative impact that small structural variations have on the similarity score. This results in a robust and efficient way to identify structural comparisons across large datasets. AVAILABILITY AND IMPLEMENTATION: The code and application guidelines of bpRNA-CosMoS are made available at github (https://github.com/BLasher113/bpRNA-CosMoS) and Zenodo (10.5281/zenodo.14715285).

Indexed as

Computational BiologyNucleic Acid ConformationRNASequence Analysis, RNASoftwareAlgorithmsBase SequenceSequence AlignmentRNA

Identifiers

PMID40085007
PMCPMC12017588

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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.