Evidence map›Paper›PMID 34103507›Full record

ArticleNature communications2021

Deep learning connects DNA traces to transcription to reveal predictive features beyond enhancer-promoter contact.

Aparna R Rajpurkar, Leslie J Mateo, Sedona E Murphy, Alistair N Boettiger

Abstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. SnapFISH-IMPUTE: an imputation method for multiplexed DNA FISH data.bioRxiv : the preprint server for biology · 2024
    Article
  8. Image-based 3D genomics through chromatin tracing.Nature reviews. Methods primers · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. 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

4 authors.

Aparna R RajpurkarDepartment of Genetics, Stanford University, Stanford, CA, USA.ORCID 0000-0003-4025-3996
Leslie J MateoDepartment of Developmental Biology, Stanford University, Stanford, CA, USA.ORCID 0000-0001-7110-3187
Sedona E MurphyDepartment of Genetics, Stanford University, Stanford, CA, USA.ORCID 0000-0001-8345-1955
Alistair N BoettigerDepartment of Developmental Biology, Stanford University, Stanford, CA, USA. boettiger@stanford.edu.ORCID 0000-0002-3554-5196

Funding

Live-cell multiplex super-resolution imaging of chromatin state transitionsU01DK127419 · NIDDK · STANFORD UNIVERSITY · PI BINTU, LACRAMIOARA, BOETTIGER, ALISTAIR N. · 2020 to 2024
$5.3M
High resolution imaging of genome structure and gene regulation in developmentDP2GM132935 · NIGMS · STANFORD UNIVERSITY · PI BOETTIGER, ALISTAIR N. · 2018 to 2018
$2.3M
NIDDK NIH HHS U01 DK127419NIGMS NIH HHS DP2 GM132935
6 · The paper itself

Abstract

Chromatin architecture plays an important role in gene regulation. Recent advances in super-resolution microscopy have made it possible to measure chromatin 3D structure and transcription in thousands of single cells. However, leveraging these complex data sets with a computationally unbiased method has been challenging. Here, we present a deep learning-based approach to better understand to what degree chromatin structure relates to transcriptional state of individual cells. Furthermore, we explore methods to "unpack the black box" to determine in an unbiased manner which structural features of chromatin regulation are most important for gene expression state. We apply this approach to an Optical Reconstruction of Chromatin Architecture dataset of the Bithorax gene cluster in Drosophila and show it outperforms previous contact-focused methods in predicting expression state from 3D structure. We find the structural information is distributed across the domain, overlapping and extending beyond domains identified by prior genetic analyses. Individual enhancer-promoter interactions are a minor contributor to predictions of activity.

Indexed as

Deep LearningEnhancer Elements, GeneticPromoter Regions, GeneticTranscription, GeneticAlgorithmsAnimalsChromatinComputer SimulationDNADrosophila melanogasterGene Expression RegulationGene SilencingGenome, InsectMultigene FamilyNeural Networks, ComputerChromatinDNA

Identifiers

PMID34103507
PMCPMC8187657

What OpenQuestion holds

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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.