Evidence map›Paper›PMID 40414878›Full record

ArticleGenome biology2025

Precise measurement of molecular phenotypes with barcode-based CRISPRi systems.

Joseph H Lobel, Nicholas T Ingolia

Abstract read
In one paragraph

Article in Genome biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. New reporters for monitoring cellular NMD.RNA (New York, N.Y.) · 2025
    Article
  4. Article
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Joseph H LobelDepartment of Molecular and Cell Biology, University of California Berkeley, Berkeley, CA, 94720, USA.
Nicholas T IngoliaDepartment of Molecular and Cell Biology, University of California Berkeley, Berkeley, CA, 94720, USA. ingolia@berkeley.edu.

Funding

High-precision pooled screening for quantitative molecular phenotypesR01GM135233 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI INGOLIA, NICHOLAS T · 2020 to 2023
$1.2M
Post-translational phenotypic profiling through nucleotide barcode sequencingR21HG012991 · NHGRI · UNIVERSITY OF CALIFORNIA BERKELEY · PI INGOLIA, NICHOLAS T · 2023 to 2024
$405k
Principles and Properties of Disordered Regions in Post-Transcriptional ControlF32GM148044 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI LOBEL, JOSEPH HEIMLICH · 2022 to 2023
$139k
NHGRI NIH HHS R21 HG012991NIGMS NIH HHS F32 GM148044NIGMS NIH HHS R01 GM135233
6 · The paper itself

Abstract

Genome-wide CRISPR-Cas9 screens have untangled regulatory networks driving diverse biological processes. Their success relies on interrogating specific molecular phenotypes and distinguishing key regulators from background effects. Here, we realize these goals by optimizing CRISPR interference with barcoded expression reporter sequencing (CiBER-seq) to dramatically improve the sensitivity and scope of genome-wide screens. We systematically address technical factors that distort phenotypic measurements by normalizing expression reporters against closely matched promoters. We use our improved CiBER-seq to accurately capture known components of well-studied RNA and protein quality control systems. These results demonstrate the precision and versatility of CiBER-seq for dissecting cellular pathways.

Indexed as

CRISPR-Cas SystemsHumansPhenotypePromoter Regions, GeneticCIBER-seqCRISPR/Cas9Massively parallel reporter assayNonsense-mediated decayProtein quality control

Identifiers

PMID40414878
PMCPMC12103760

What OpenQuestion holds

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LicenceCC BY
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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.