Evidence map›Paper›PMID 39713364›Full record

ArticlebioRxiv : the preprint server for biology2024

L2G: Repurposing Language Models for Genomics Tasks.

Wenduo Cheng, Junhong Shen, Mikhail Khodak, Jian Ma, Ameet Talwalkar

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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
–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

5 authors.

Wenduo ChengRay and Stephanie Lane Computational Biology Department, School of Computer Science, Carnegie Mellon University, Pittsburgh, PA 15213, USA.
Junhong ShenMachine Learning Department, School of Computer Science, Carnegie Mellon University, Pittsburgh, PA 15213, USA.
Mikhail KhodakPrinceton Language & Intelligence, Princeton AI Lab, Princeton University, Princeton, NJ 08544, USA.
Jian MaRay and Stephanie Lane Computational Biology Department, School of Computer Science, Carnegie Mellon University, Pittsburgh, PA 15213, USA.ORCID 0000-0002-4202-5834
Ameet TalwalkarMachine Learning Department, School of Computer Science, Carnegie Mellon University, Pittsburgh, PA 15213, USA.ORCID 0000-0001-6650-1893

Funding

Multiscale Analyses of 4D Nucleome Structure and Function by Comprehensive Multimodal Data IntegrationUM1HG011593 · NHGRI · CARNEGIE-MELLON UNIVERSITY · PI ALBER, FRANK, BELMONT, ANDREW STEVEN · 2020 to 2024
$10.4M
WashU-Northwestern Genomic Variation and Function Data and Administrative Coordinating CenterU24HG012070 · NHGRI · WASHINGTON UNIVERSITY · PI Ting Wang, Feng Yue · 2021 to 2026
$9.7M
Computational Methods for Next-Generation Comparative GenomicsR01HG007352 · NHGRI · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI MA, JIAN · 2014 to 2023
$2.8M
Computational methods for studying single-cell 3D genomeR01HG012303 · NHGRI · CARNEGIE-MELLON UNIVERSITY · PI DUAN, ZHIJUN, MA, JIAN · 2022 to 2025
$2.2M
Spatial omics technologies to map the senescent cell microenvironmentUH3CA268202 · NCI · BROWN UNIVERSITY · PI MA, JIAN, NERETTI, NICOLA · 2023 to 2025
$2.2M
Three-dimensional mapping and modeling of combinatorial interactions underlying biomolecular condensates in olfactory neuronsR21DA061481 · NIDA · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI GUTTMAN, MITCHELL, LOMVARDAS, STAVROS · 2024 to 2025
$465k
NCI NIH HHS UH3 CA268202NHGRI NIH HHS R01 HG007352NHGRI NIH HHS R01 HG012303NHGRI NIH HHS U24 HG012070NHGRI NIH HHS UM1 HG011593NIDA NIH HHS R21 DA061481
6 · The paper itself

Abstract

Pre-trained language models have transformed the field of natural language processing (NLP), and their success has inspired efforts in genomics to develop domain-specific foundation models (FMs). However, creating high-quality genomic FMs from scratch is resource-intensive, requiring significant computational power and high-quality pre-training data. The success of large language models (LLMs) in NLP has largely been driven by industrial-scale efforts leveraging vast, diverse corpora and massive computing infrastructure. In this work, we aim to bypass the data and computational bottlenecks of creating genomic FMs from scratch and instead propose repurposing existing LLMs for genomics tasks. Inspired by the recently observed 'cross-modal transfer' phenomenon - where transformers pre-trained on natural language can generalize to other modalities - we introduce L2G, which adapts a pre-trained LLM architecture for genomics using neural architecture search (NAS) and a novel three-stage training procedure. Remarkably, without requiring extensive pre-training on DNA sequence data, L2G achieves superior performance to fine-tuned genomic FMs and task-specific models on more than half of tasks across multiple genomics benchmarks. In an enhancer activity prediction task, L2G further demonstrates its capacity to identify significant transcription factor motifs. Our work not only highlights the generalizability and efficacy of language models in out-of-domain tasks such as genomics, but also opens new avenues for more efficient and less resource-intensive methodologies in genomic research.

Identifiers

PMID39713364
PMCPMC11661171

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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.