Evidence map›Paper›PMID 39745647›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2025

Single-Cell Profiling of Lineages and Cell Types in the Vertebrate Brain.

Bushra Raj

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Modern Mining: The Role of Single-cell RNA Sequencing in Advancing Neuroscience Research.BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
    Review
  2. Review
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

1 author.

Bushra RajDepartment of Cell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA. bushra.raj@pennmedicine.upenn.edu.

Funding

Genomic tools for massively parallel recording of signaling activity at cellular resolution in a brain-wide mannerDP2NS131787 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI RAJ, BUSHRA · 2022 to 2025
$2.4M
Investigating progenitor cell development and lineage relationships in the brainR00HD098298 · NICHD · UNIVERSITY OF PENNSYLVANIA · PI RAJ, BUSHRA · 2021 to 2023
$747k
NICHD NIH HHS R00 HD098298NINDS NIH HHS DP2 NS131787
6 · The paper itself

Abstract

CRISPR-Cas tools have recently been adapted for cell lineage tracing during development. Combined with single-cell RNA sequencing, these methods enable scalable lineage tracing with single-cell resolution. Here, I describe, scGESTALTv2, which combines cumulative CRISPR-Cas9 editing of a lineage barcode array with transcriptional profiling via droplet-based single-cell RNA sequencing (scRNA-seq). The technique is applied in developing zebrafish brains to generate mutations in the barcode array during development. The recorded lineages along with cellular transcriptomes are then extracted via scRNA-seq to define cell relationships among thousands of profiled brain cells and dozens of cell types.

Indexed as

BrainCell LineageCRISPR-Cas SystemsGene EditingSingle-Cell AnalysisZebrafishAnimalsGene Expression ProfilingTranscriptomeBarcodingBrain dissociationCRISPR-Cas9GeneticsLineage tracingNeurodevelopmentscRNA-seqSingle cellZebrafish

Identifiers

What OpenQuestion holds

Textmetadata
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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.