Evidence map›Paper›PMID 42282737›Full record

ArticlebioRxiv : the preprint server for biology2026

Gigabase-scale deletion scanning of the human genome.

Jonas Koeppel, Aidan Keith, Samantha Sgrizzi, Peixi Chen, Riza M Daza, Faaiz Quaisar, Eleftheria Anastasia, Zihao Song, Jay Shendure, Sudarshan Pinglay

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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

10 authors.

Jonas KoeppelDepartment of Genome Sciences, University of Washington, Seattle, WA 98195, USA.ORCID 0000-0003-1306-3994
Aidan KeithDepartment of Genome Sciences, University of Washington, Seattle, WA 98195, USA.ORCID 0000-0002-2675-5538
Samantha SgrizziSeattle Hub for Synthetic Biology, Seattle, WA 98109, USA.ORCID 0000-0001-5414-3160
Peixi ChenDepartment of Genome Sciences, University of Washington, Seattle, WA 98195, USA.ORCID 0000-0002-7584-4609
Riza M DazaDepartment of Genome Sciences, University of Washington, Seattle, WA 98195, USA.ORCID 0000-0003-1635-8675
Faaiz QuaisarDepartment of Genome Sciences, University of Washington, Seattle, WA 98195, USA.
Eleftheria AnastasiaSeattle Hub for Synthetic Biology, Seattle, WA 98109, USA.ORCID 0009-0004-5593-0448
Zihao SongSeattle Hub for Synthetic Biology, Seattle, WA 98109, USA.
Jay ShendureDepartment of Genome Sciences, University of Washington, Seattle, WA 98195, USA.ORCID 0000-0002-1516-1865
Sudarshan PinglayDepartment of Genome Sciences, University of Washington, Seattle, WA 98195, USA.ORCID 0000-0002-8781-1476

Funding

Supplement for Center for Synthetic Regulatory Genomics: Building CACNA1C alleles associated with Neuropsychiatric DisordersRM1HG009491 · NHGRI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Jef D BOEKE · 2018 to 2026
$20.9M
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
Dissecting the logic of mammalian gene regulation using synthetic biology and single-cell sequencingDP5OD036167 · OD · UNIVERSITY OF WASHINGTON · PI Sudarshan Pinglay · 2023 to 2026
$1.9M
NHGRI NIH HHS R01 HG010632NHGRI NIH HHS RM1 HG009491NIH HHS DP5 OD036167
6 · The paper itself

Abstract

What fraction of the human genome is essential for cellular viability? To date, essentiality in human cells has been mapped almost exclusively at the level of individual open reading frames (ORFs). Whether non-coding regions and broader architectural features of the genome are required for human cells to remain viable, and where the boundaries of any such regions lie, remains largely unexplored. Here we introduce Shred-seq, which couples Type I-C CRISPR-Cas3-mediated deletions with phage polymerase-based genotyping to enable large-scale deletion scans of the human genome. Shred-seq leverages thousands of genomically integrated, mapped target sites as launchpads for Cas3 to initiate unidirectional deletions ranging in size from hundreds of base pairs (bp) to hundreds of kb. Breakpoints are directly captured at high resolution by

Identifiers

PMID42282737
PMCPMC13251986

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.