Evidence map›Paper›PMID 41673323›Full record

ReviewNature protocols2026

Multichannel genomic recording of biological information with ENGRAM.

Jenny F Nathans, Troy A McDiarmid, Wei Chen, Jay Shendure

Abstract readReview
In one paragraph

Review in Nature protocols, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Jenny F Nathans *Department of Genome Sciences, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-0276-734X
Troy A McDiarmid *Department of Genome Sciences, University of Washington, Seattle, WA, USA. troym13@uw.edu.ORCID http://orcid.org/0000-0002-4893-9733
Wei Chen *Seattle Hub for Synthetic Biology, Seattle, WA, USA. wchen108@uw.edu.ORCID http://orcid.org/0000-0002-5255-4166
Jay ShendureDepartment of Genome Sciences, University of Washington, Seattle, WA, USA. shendure@uw.edu.ORCID http://orcid.org/0000-0002-1516-1865

Funding

Versatile, exponentially scalable methods for single cell molecular profilingR01HG010632 · NHGRI · UNIVERSITY OF WASHINGTON · PI Jay Ashok Shendure, Bruce Colston Trapnell · 2019 to 2026
$5.9M
Spatially resolved mapping of lineage and signaling history in human skin organoidsF31AR084852 · NIAMS · UNIVERSITY OF WASHINGTON · PI Jenny Nathans · 2025 to 2026
$88k
Damon Runyon Cancer Research Foundation (Cancer Research Fund of the Damon Runyon-Walter Winchell Foundation) DRG-2507-23Howard Hughes Medical InstituteNHGRI NIH HHS R01 HG010632NIAMS NIH HHS F31 AR084852U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute (NHGRI) R01HG010632
6 · The paper itself

Abstract

Molecular recording is an emerging paradigm for measuring biology over time. Enhancer-mediated genomic recording of activity in multiplex (ENGRAM) is a recently described synthetic biology circuit architecture that converts the transient activity of cis-regulatory elements (CREs) into stable genomic records that can be retrospectively recovered via DNA sequencing. Here we provide a step-by-step protocol for conducting ENGRAM experiments and analyzing the resulting data. We also describe key design considerations for ENGRAM recorders, summarize the strengths and limitations of ENGRAM, and highlight applications, including multiplex signal recording and high-throughput CRE screening. In contrast to other systems for DNA-based recording in mammalian systems, ENGRAM relies on prime editing-mediated insertions to record the activity of a given CRE, such that it is inherently multiplexable-for example, four-base-pair insertions can represent the activities of up to 256 distinct CREs. A further contrast lies with ENGRAM's compatibility with DNA Typewriter, which facilitates the capture of signal order. For users with basic skills in molecular biology, mammalian cell culture and DNA sequencing analysis, ENGRAM experiments can typically be completed within 5-6 weeks.

Indexed as

GenomicsSynthetic BiologyAnimalsIntegrasesSequence Analysis, DNACre recombinaseIntegrases

Identifiers

PMID41673323
PMCPMC13150845

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.