Evidence map›Paper›PMID 31484777›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

A computational framework for DNA sequencing microscopy.

Ian T Hoffecker, Yunshi Yang, Giulio Bernardinelli, Pekka Orponen, Björn Högberg

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
  2. Article
  3. Spatial coherence in DNA barcode networks.Patterns (New York, N.Y.) · 2025
    Article
  4. Article
  5. Article
  6. Optics-free reconstruction of 2D images via DNA barcode proximity graphs.bioRxiv : the preprint server for biology · 2024
    Article
  7. Article
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  10. Review
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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

5 authors.

Ian T HoffeckerDepartment of Medical Biochemistry and Biophysics, Karolinska Institutet, S-17177 Stockholm, Sweden.ORCID 0000-0001-6941-4576
Yunshi YangDepartment of Medical Biochemistry and Biophysics, Karolinska Institutet, S-17177 Stockholm, Sweden.
Giulio BernardinelliDepartment of Medical Biochemistry and Biophysics, Karolinska Institutet, S-17177 Stockholm, Sweden.ORCID 0000-0002-3394-7976
Pekka OrponenDepartment of Computer Science, Aalto University, FI-00076 Aalto, Finland.
Björn HögbergDepartment of Medical Biochemistry and Biophysics, Karolinska Institutet, S-17177 Stockholm, Sweden; bjorn.hogberg@ki.se.ORCID 0000-0003-2715-7887

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We describe a method whereby microscale spatial information such as the relative positions of biomolecules on a surface can be transferred to a sequence-based format and reconstructed into images without conventional optics. Barcoded DNA "polymerase colony" (polony) amplification techniques enable one to distinguish specific locations of a surface by their sequence. Image formation is based on pairwise fusion of uniquely tagged and spatially adjacent polonies. The network of polonies connected by shared borders forms a graph whose topology can be reconstructed from pairs of barcodes fused during a polony cross-linking phase, the sequences of which are determined by recovery from the surface and next-generation (next-gen) sequencing. We developed a mathematical and computational framework for this principle called polony adjacency reconstruction for spatial inference and topology and show that Euclidean spatial data may be stored and transmitted in the form of graph topology. Images are formed by transferring molecular information from a surface of interest, which we demonstrated in silico by reconstructing images formed from stochastic transfer of hypothetical molecular markers. The theory developed here could serve as a basis for an automated, multiplexable, and potentially superresolution imaging method based purely on molecular information.

Indexed as

MicroscopyComputational BiologyComputer SimulationGenetic CodeHigh-Throughput Nucleotide SequencingImage Processing, Computer-AssistedPolymerase Chain ReactionSequence Analysis, DNADNA computingDNA microscopygraph theorynext-gen sequencingpolonies

Identifiers

PMID31484777
PMCPMC6765314

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.