Evidence map›Paper›PMID 36593410›Full record

ArticleNature biotechnology2023

A spatial genome aligner for resolving chromatin architectures from multiplexed DNA FISH.

Bojing Blair Jia, Adam Jussila, Colin Kern, Quan Zhu, Bing Ren

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Nature biotechnology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
6.5field-weighted citation impact, top 3% of its field
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

23 citing papers in PubMed, 38 citations in OpenAlex.

  1. Differential analysis of image-based chromatin tracing data with Dory.bioRxiv : the preprint server for biology · 2026
    Article
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  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Image Analysis Protocol for DNA/RNA/Immunofluorescence (IF)-seqFISH Data.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  11. Measurement of Spatial Contact Map Using Sequential FISH.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  12. Article
  13. Epigenetics and the timing of neuronal differentiation.Current opinion in neurobiology · 2024
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. SnapFISH-IMPUTE: an imputation method for multiplexed DNA FISH data.bioRxiv : the preprint server for biology · 2024
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

Bojing Blair JiaBioinformatics and Systems Biology Graduate Program, University of California San Diego, La Jolla, CA, USA.
Adam JussilaBioinformatics and Systems Biology Graduate Program, University of California San Diego, La Jolla, CA, USA.
Colin KernDepartment of Cellular and Molecular Medicine, Center for Epigenomics, University of California San Diego, La Jolla, CA, USA.
Quan ZhuDepartment of Cellular and Molecular Medicine, Center for Epigenomics, University of California San Diego, La Jolla, CA, USA.
Bing RenDepartment of Cellular and Molecular Medicine, Center for Epigenomics, University of California San Diego, La Jolla, CA, USA. biren@health.ucsd.edu.ORCID 0000-0002-5435-1127
University of California San Diego · USLudwig Cancer Research · BE

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007198 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHI, NEIL C, INSEL, PAUL A · 1985 to 2024
$29.3M
Training Program in Basic Clinical GeneticsT32GM008666 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HAMILTON, BRUCE A · 1998 to 2021
$8.6M
Center for Integrated Multi-modal and Multi-scale Nucleome ResearchUM1HG011585 · NHGRI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DULAC, CATHERINE, LEIN, ED · 2020 to 2024
$6.7M
UC San Diego Medical Scientist Training ProgramT32GM154642 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Neil C Chi, Mary Kathleen Lewinski · 2025 to 2026
$2.9M
NHGRI NIH HHS UM1 HG011585NIGMS NIH HHS T32 GM007198NIGMS NIH HHS T32 GM008666NIGMS NIH HHS T32 GM154642
6 · The paper itself

Abstract

Multiplexed fluorescence in situ hybridization (FISH) is a widely used approach for analyzing three-dimensional genome organization, but it is challenging to derive chromosomal conformations from noisy fluorescence signals, and tracing chromatin is not straightforward. Here we report a spatial genome aligner that parses true chromatin signal from noise by aligning signals to a DNA polymer model. Using genomic distances separating imaged loci, our aligner estimates spatial distances expected to separate loci on a polymer in three-dimensional space. Our aligner then evaluates the physical probability observed signals belonging to these loci are connected, thereby tracing chromatin structures. We demonstrate that this spatial genome aligner can efficiently model chromosome architectures from DNA FISH data across multiple scales and be used to predict chromosome ploidies de novo in interphase cells. Reprocessing of previous whole-genome chromosome tracing data with this method indicates the spatial aggregation of sister chromatids in S/G2 phase cells in asynchronous mouse embryonic stem cells and provides evidence for extranumerary chromosomes that remain tightly paired in postmitotic neurons of the adult mouse cortex.

Indexed as

ChromatinChromosomesAnimalsDNAIn Situ Hybridization, FluorescenceMicePolymersChromatinDNAPolymers

Identifiers

PMID36593410
PMCPMC10344783
OpenAlexW4313454162

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.