Evidence map›Paper›PMID 39416135›Full record

ArticlebioRxiv : the preprint server for biology2025

Orthrus: Towards Evolutionary and Functional RNA Foundation Models.

Philip Fradkin, Ruian Shi, Taykhoom Dalal, Keren Isaev, Brendan J Frey, Leo J Lee, Quaid Morris, Bo Wang

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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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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

5 · Who and what money

Authors and funding

8 authors.

Philip FradkinVector Institute, Ontario, Canada.
Ruian ShiVector Institute, Ontario, Canada.
Taykhoom DalalComputational and Systems Biology Program, Sloan Kettering Institute, New York, United States.
Keren IsaevNew York Genome Center, New York, United States.
Brendan J FreyVector Institute, Ontario, Canada.
Leo J LeeVector Institute, Ontario, Canada.ORCID 0000-0003-1829-1187
Quaid MorrisComputational and Systems Biology Program, Sloan Kettering Institute, New York, United States.
Bo WangVector Institute, Ontario, Canada.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Post-transcriptional Regulatory NetworksR01HG013328 · NHGRI · SLOAN-KETTERING INST CAN RESEARCH · PI Quaid Morris · 2023 to 2026
$2.6M
NCI NIH HHS P30 CA008748NHGRI NIH HHS R01 HG013328
6 · The paper itself

Abstract

In the face of rapidly accumulating genomic data, our ability to accurately predict key mature RNA properties that underlie transcript function and regulation remains limited. Pre-trained genomic foundation models offer an avenue to adapt learned RNA representations to biological prediction tasks. However, existing genomic foundation models are trained using strategies borrowed from textual domains that do not leverage biological domain knowledge. Here, we introduce Orthrus, a Mamba-based mature RNA foundation model pre-trained using a novel self-supervised contrastive learning objective with biological augmentations. Orthrus is trained by maximizing embedding similarity between curated pairs of RNA transcripts, where pairs are formed from splice isoforms of 10 model organisms and transcripts from orthologous genes in 400+ mammalian species from the Zoonomia Project. This training objective results in a latent representation that clusters RNA sequences with functional and evolutionary similarities. We find that the generalized mature RNA isoform representations learned by Orthrus significantly outperform genomic foundation models on mRNA property prediction tasks, and requires only a fraction of fine-tuning data to do so. Finally, we show that Orthrus is capable of capturing divergent biological function of individual transcript isoforms.

Identifiers

PMID39416135
PMCPMC11482885

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LicenceCC BY
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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.