Evidence map›Paper›PMID 38177592›Full record

ArticleNature computational science2023

Predictive analyses of regulatory sequences with EUGENe.

Adam Klie, David Laub, James V Talwar, Hayden Stites, Tobias Jores, Joe J Solvason, Emma K Farley, Hannah Carter

Abstract read
In one paragraph

Article in Nature computational science, 2023. 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. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Analysis-ready VCF at Biobank scale using Zarr.bioRxiv : the preprint server for biology · 2025
    Article
  11. Article
  12. Article
  13. Review
  14. bioRxiv : the preprint server for biology · 2024
    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

8 authors.

Adam KlieDepartment of Medicine, University of California San Diego, La Jolla, CA, USA.ORCID 0000-0002-7600-3086
David LaubDepartment of Medicine, University of California San Diego, La Jolla, CA, USA.
James V TalwarDepartment of Medicine, University of California San Diego, La Jolla, CA, USA.
Hayden StitesDaniel Hand High School, Madison, CT, USA.
Tobias JoresDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.ORCID 0000-0002-1804-7187
Joe J SolvasonDepartment of Medicine, University of California San Diego, La Jolla, CA, USA.
Emma K FarleyDepartment of Medicine, University of California San Diego, La Jolla, CA, USA.
Hannah CarterDepartment of Medicine, University of California San Diego, La Jolla, CA, USA. hkcarter@ucsd.edu.ORCID 0000-0002-1729-2463

Funding

TR&D 3 - Network Guided Machine LearningP41GM103504 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI PICO, ALEXANDER R · 2012 to 2024
$17.3M
San Diego Biomedical Informatics Education & Research (SABER)T15LM011271 · NLM · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SHAMIM NEMATI · 2012 to 2026
$9.7M
The Common Fund Knowledge Center (CFKC): providing scientifically valid knowledge from the Common Fund Data Ecosystem to the biomedical research communityOT2OD036440 · OD · BROAD INSTITUTE, INC. · PI Noel P Burtt, Jason Flannick · 2023 to 2026
$8.5M
The impact of genomic variation on environment-induced changes in pancreatic beta cell statesU01HG012059 · NHGRI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Hannah Kathryn Carter, Kyle Jeffrie Gaulton · 2021 to 2026
$7.5M
Deciphering the regulatory principles governing enhancer specificityDP2HG010013 · NHGRI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FARLEY, EMMA KIRSTEN · 2017 to 2021
$2.5M
NHGRI NIH HHS DP2 HG010013NHGRI NIH HHS U01 HG012059NIGMS NIH HHS P41 GM103504NIH HHS OT2 OD036440NLM NIH HHS T15 LM011271
6 · The paper itself

Abstract

Deep learning has become a popular tool to study cis-regulatory function. Yet efforts to design software for deep-learning analyses in regulatory genomics that are findable, accessible, interoperable and reusable (FAIR) have fallen short of fully meeting these criteria. Here we present elucidating the utility of genomic elements with neural nets (EUGENe), a FAIR toolkit for the analysis of genomic sequences with deep learning. EUGENe consists of a set of modules and subpackages for executing the key functionality of a genomics deep learning workflow: (1) extracting, transforming and loading sequence data from many common file formats; (2) instantiating, initializing and training diverse model architectures; and (3) evaluating and interpreting model behavior. We designed EUGENe as a simple, flexible and extensible interface for streamlining and customizing end-to-end deep-learning sequence analyses, and illustrate these principles through application of the toolkit to three predictive modeling tasks. We hope that EUGENe represents a springboard towards a collaborative ecosystem for deep-learning applications in genomics research.

Indexed as

GenomicsGenomeSoftwareWorkflow

Identifiers

PMID38177592
PMCPMC10768637

What OpenQuestion holds

Textmetadata
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.