Evidence map›Paper›PMID 38352499›Full record

ArticlebioRxiv : the preprint server for biology2024

DNA-Diffusion: Leveraging Generative Models for Controlling Chromatin Accessibility and Gene Expression via Synthetic Regulatory Elements.

Lucas Ferreira DaSilva, Simon Senan, Zain Munir Patel, Aniketh Janardhan Reddy, Sameer Gabbita, Zach Nussbaum, César Miguel Valdez Córdova, Aaron Wenteler, Noah Weber, Tin M Tunjic and 10 more

Open access · greenAbstract 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. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. The design and engineering of synthetic genomes.Nature reviews. Genetics · 2025
    Review
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

20 authors at 9 institutions in 5 countries.

Lucas Ferreira DaSilvaDepartment of Pathology, Harvard Medical School, Boston, MA, USA.
Simon SenanMolecular Pathology Unit, Center for Cancer Research, Massachusetts General Hospital, Boston, MA, USA.
Zain Munir PatelDepartment of Pathology, Harvard Medical School, Boston, MA, USA.
Aniketh Janardhan ReddyDepartment of Electrical Engineering and Computer Sciences, University of California, Berkeley, CA, USA.
Sameer GabbitaMolecular Pathology Unit, Center for Cancer Research, Massachusetts General Hospital, Boston, MA, USA.
Zach NussbaumNomic AI.
César Miguel Valdez CórdovaJohannes Kepler University, Linz, Austria.
Aaron WentelerQueen Mary University of London, London, UK.
Noah WeberTU Vienna, Austria.
Tin M TunjicTU Vienna, Austria.
Talha Ahmad KhanIndependent Researcher.
Zelun LiVictor Chang Cardiac Institute, Darlinghurst, New South Wales, Australia.
Cameron SmithDepartment of Pathology, Harvard Medical School, Boston, MA, USA.
Matei BejanUniversity of Bucharest, Bucharest, Romania.
Lithin Karmel LouisVictor Chang Cardiac Institute, Darlinghurst, New South Wales, Australia.
Paola CornejoVictor Chang Cardiac Institute, Darlinghurst, New South Wales, Australia.
Will ConnellIndependent Researcher.
Emily S WongVictor Chang Cardiac Institute, Darlinghurst, New South Wales, Australia.
Wouter MeulemanAltius Institute for Biomedical Sciences, Seattle, WA, USA.
Luca PinelloDepartment of Pathology, Harvard Medical School, Boston, MA, USA.ORCID 0000-0003-1109-3823
Broad Institute · USVictor Chang Cardiac Research Institute · AUHarvard University · USJohannes Kepler University of Linz · ATJohns Hopkins University · USQueen Mary University of London · GBUniversity of Bucharest · ROUniversity of California, Berkeley · USUniversity of Washington · US

Funding

Multiscale exploration of the functional non-coding genomeR35HG010717 · NHGRI · MASSACHUSETTS GENERAL HOSPITAL · PI PINELLO, LUCA · 2019 to 2023
$2.6M
Elucidation of the organizing principles of the regulatory genome through large-scale data integrationR35HG011317 · NHGRI · ALTIUS INSTITUTE FOR BIOMEDICAL SCIENCES · PI MEULEMAN, WOUTER · 2020 to 2024
$1.8M
NHGRI NIH HHS R35 HG010717NHGRI NIH HHS R35 HG011317
6 · The paper itself

Abstract

The challenge of systematically modifying and optimizing regulatory elements for precise gene expression control is central to modern genomics and synthetic biology. Advancements in generative AI have paved the way for designing synthetic sequences with the aim of safely and accurately modulating gene expression. We leverage diffusion models to design context-specific DNA regulatory sequences, which hold significant potential toward enabling novel therapeutic applications requiring precise modulation of gene expression. Our framework uses a cell type-specific diffusion model to generate synthetic 200 bp regulatory elements based on chromatin accessibility across different cell types. We evaluate the generated sequences based on key metrics to ensure they retain properties of endogenous sequences: transcription factor binding site composition, potential for cell type-specific chromatin accessibility, and capacity for sequences generated by DNA diffusion to activate gene expression in different cell contexts using state-of-the-art prediction models. Our results demonstrate the ability to robustly generate DNA sequences with cell type-specific regulatory potential. DNA-Diffusion paves the way for revolutionizing a regulatory modulation approach to mammalian synthetic biology and precision gene therapy.

Identifiers

PMID38352499
PMCPMC10862870
OpenAlexW4391482904

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.