Evidence map›Paper›PMID 42185539›Full record

ArticleNature methods2026

Decoding sequence determinants of gene expression in diverse cellular and disease states.

Avantika Lal, Alexander Karollus, Laura Gunsalus, David Garfield, Surag Nair, Alex M Tseng, M Grace Gordon, John Blischak, Bryce Van De Geijn, Tushar Bhangale and 6 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature methods, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

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  5. Article
  6. Teaching an old dog new cells.Nature methods · 2026
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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

16 authors.

Avantika Lal *Biology Research | AI Development, gRED Computational Sciences, Genentech, South San Francisco, CA, USA. lal.avantika@gene.com.ORCID http://orcid.org/0000-0002-5827-0826
Alexander Karollus *Biology Research | AI Development, gRED Computational Sciences, Genentech, South San Francisco, CA, USA.
Laura GunsalusBiology Research | AI Development, gRED Computational Sciences, Genentech, South San Francisco, CA, USA.ORCID http://orcid.org/0000-0003-3444-5617
David GarfieldOMNI Bioinformatics and Department of Regenerative Medicine, Genentech, South San Francisco, CA, USA.
Surag NairBiology Research | AI Development, gRED Computational Sciences, Genentech, South San Francisco, CA, USA.ORCID http://orcid.org/0000-0002-6216-2457
Alex M TsengBiology Research | AI Development, gRED Computational Sciences, Genentech, South San Francisco, CA, USA.
M Grace GordonDepartment of Cellular and Tissue Genomics, Genentech Research and Early Development, Genentech, South San Francisco, CA, USA.ORCID http://orcid.org/0000-0003-4321-9187
John BlischakDepartment of Human Genetics, Genentech, South San Francisco, CA, USA.
Bryce Van De GeijnDepartment of Human Genetics, Genentech, South San Francisco, CA, USA.
Tushar BhangaleDepartment of Human Genetics, Genentech, South San Francisco, CA, USA.
Jenna L CollierBiology Research | AI Development, gRED Computational Sciences, Genentech, South San Francisco, CA, USA.ORCID http://orcid.org/0000-0002-4071-4986
Nathaniel DiamantBiology Research | AI Development, gRED Computational Sciences, Genentech, South San Francisco, CA, USA.
Tommaso BiancalaniBiology Research | AI Development, gRED Computational Sciences, Genentech, South San Francisco, CA, USA.ORCID http://orcid.org/0000-0001-9104-9755
Hector Corrada BravoBiology Research | AI Development, gRED Computational Sciences, Genentech, South San Francisco, CA, USA.
Gabriele ScaliaBiology Research | AI Development, gRED Computational Sciences, Genentech, South San Francisco, CA, USA.ORCID http://orcid.org/0000-0003-3305-9220
Gokcen EraslanBiology Research | AI Development, gRED Computational Sciences, Genentech, South San Francisco, CA, USA. eraslan.gokcen@gene.com.ORCID http://orcid.org/0000-0001-9579-2909

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sequence-to-function models that predict gene expression from genomic DNA sequence have proven valuable for many biological tasks, including understanding cis-regulatory syntax and interpreting noncoding genetic variation. However, current state-of-the-art models are trained largely on bulk expression profiles from healthy tissues or cell lines and have not learned the properties of precise cell types and states that are captured in large-scale single-cell transcriptomic datasets. Thus, they cannot perform these tasks at the resolution of specific cell types or states. Here we present Decima, a model that predicts the cell type- and condition-specific expression of a gene from its surrounding DNA sequence. Decima is trained on single-cell or single-nucleus RNA sequencing data from over 22 million cells and successfully predicts the cell-type-specific expression of unseen genes. We demonstrate Decima's ability to reveal cis-regulatory mechanisms driving cell-type-specific gene expression and its changes in disease, predict noncoding-variant effects at cell type resolution and design context-specific regulatory DNA elements.

Indexed as

Gene Expression RegulationAnimalsHumansRegulatory Sequences, Nucleic AcidSingle-Cell Gene Expression Analysis

Identifiers

What OpenQuestion holds

Textmetadata
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.