Evidence map›Paper›PMID 31740838›Full record

ArticleNature biotechnology2020

In situ readout of DNA barcodes and single base edits facilitated by in vitro transcription.

Amjad Askary, Luis Sanchez-Guardado, James M Linton, Duncan M Chadly, Mark W Budde, Long Cai, Carlos Lois, Michael B Elowitz

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Nature biotechnology, 2020. 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 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

63 citing papers in PubMed, 99 citations in OpenAlex.

  1. Article
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  6. Gigabase-scale deletion scanning of the human genome.bioRxiv : the preprint server for biology · 2026
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  17. Mitochondrial clone tracing within spatially intact human tissues.bioRxiv : the preprint server for biology · 2025
    Article
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  19. Article
  20. Article

3 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Amjad AskaryDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA.
Luis Sanchez-GuardadoDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA.
James M LintonDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA.
Duncan M ChadlyDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA.
Mark W BuddeDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA.
Long CaiDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA.ORCID http://orcid.org/0000-0002-7154-5361
Carlos LoisDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA.
Michael B ElowitzDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA. melowitz@caltech.edu.ORCID http://orcid.org/0000-0002-1221-0967
California Institute of Technology · US

Funding

PREDOCTORAL TRAINING IN BIOLOGY AND CHEMISTRYT32GM007616 · NIGMS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI STERNBERG, PAUL WARREN · 1985 to 2019
$22.9M
MEMOIR: Recording, and in situ readout of cell lineage and transcriptional historyR01MH116508 · NIMH · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI CAI, LONG, ELOWITZ, MICHAEL B · 2017 to 2021
$6.9M
Howard Hughes Medical InstituteNIGMS NIH HHS T32 GM007616NIMH NIH HHS R01 MH116508
6 · The paper itself

Abstract

Molecular barcoding technologies that uniquely identify single cells are hampered by limitations in barcode measurement. Readout by sequencing does not preserve the spatial organization of cells in tissues, whereas imaging methods preserve spatial structure but are less sensitive to barcode sequence. Here we introduce a system for image-based readout of short (20-base-pair) DNA barcodes. In this system, called Zombie, phage RNA polymerases transcribe engineered barcodes in fixed cells. The resulting RNA is subsequently detected by fluorescent in situ hybridization. Using competing match and mismatch probes, Zombie can accurately discriminate single-nucleotide differences in the barcodes. This method allows in situ readout of dense combinatorial barcode libraries and single-base mutations produced by CRISPR base editors without requiring barcode expression in live cells. Zombie functions across diverse contexts, including cell culture, chick embryos and adult mouse brain tissue. The ability to sensitively read out compact and diverse DNA barcodes by imaging will facilitate a broad range of barcoding and genomic recording strategies.

Indexed as

Gene EditingTranscription, GeneticAnimalsBase PairingBase SequenceBrainChick EmbryoDNA Barcoding, TaxonomicDNA-Directed RNA PolymerasesGene LibraryHEK293 CellsHumansLentivirusMiceNucleotidesPolymorphism, Single NucleotideDNA-Directed RNA PolymerasesNucleotides

Identifiers

PMID31740838
PMCPMC6954335
OpenAlexW2985708835

What OpenQuestion holds

Textmetadata
LicenceTDM
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.