Evidence map›Paper›PMID 42401553›Full record

ArticleNature communications2026

Positional interpretation of cis-regulatory code and nucleosome organization with deep learning models.

Charles E McAnany, Melanie Weilert, Grishma Mehta, Fahad Kamulegeya, Jennifer M Gardner, Jacob Schreiber, Anshul Kundaje, Julia Zeitlinger

Abstract read
In one paragraph

Article in Nature communications, 2026. 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.

  1. AlphaGenome Atlas:medRxiv : the preprint server for health sciences · 2026
    Article
  2. 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.

Charles E McAnanyStowers Institute for Medical Research, Kansas City, MO, USA.
Melanie WeilertStowers Institute for Medical Research, Kansas City, MO, USA.
Grishma MehtaStowers Institute for Medical Research, Kansas City, MO, USA.
Fahad KamulegeyaStowers Institute for Medical Research, Kansas City, MO, USA.
Jennifer M GardnerStowers Institute for Medical Research, Kansas City, MO, USA.
Jacob SchreiberResearch Institute of Molecular Pathology, Vienna BioCenter, Vienna, Austria.ORCID http://orcid.org/0000-0003-4230-6625
Anshul KundajeDepartment of Genetics, Stanford University, Palo Alto, CA, USA.ORCID http://orcid.org/0000-0003-3084-2287
Julia ZeitlingerStowers Institute for Medical Research, Kansas City, MO, USA. jbz@stowers.org.ORCID http://orcid.org/0000-0002-5172-3335

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sequence-to-function neural networks learn cis-regulatory sequence rules driving many types of genomic data. Interpreting these models to relate the sequence rules to underlying biological processes remains challenging, especially for complex genomic readouts such as MNase-seq, which maps nucleosome occupancy but is confounded by experimental bias. Here, we introduce pairwise influence by sequence attribution (PISA), which uses attribution to combinatorially decode which bases contributed to the readout at a specific genomic coordinate. PISA visualizes the effects of transcription factor motifs, detects undiscovered motifs with complex contribution patterns, and reveals experimental biases. By learning the bias for MNase-seq, PISA enables unprecedented nucleosome prediction models. These models allow the de novo discovery of nucleosome-positioning motifs and reveal the basis of Micro-C chromatin domain boundaries through systematic motif perturbations. Finally, these models allow the design of sequences with altered nucleosome configurations. These results show that PISA is a versatile tool that expands our ability to train and interpret sequence-to-function neural networks on genomics data and understand the underlying cis-regulatory code.

Indexed as

Deep LearningNucleosomesRegulatory Sequences, Nucleic AcidAnimalsChromatinGenomicsHumansNeural Networks, ComputerNucleotide MotifsTranscription FactorsChromatinNucleosomesTranscription Factors

Identifiers

PMID42401553
PMCPMC13469612

What OpenQuestion holds

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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.