Evidence map›Paper›PMID 39976408›Full record

ArticlePhilosophical transactions of the Royal Society of London. Series B, Biological sciences2025

A Bayesian phylodynamic inference framework for single-cell CRISPR/Cas9 lineage tracing barcode data with dependent target sites.

A Zwaans, S Seidel, M Manceau, T Stadler

Abstract read
In one paragraph

Article in Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. "A mathematical theory of evolution": phylogenetic models dating back 100 years.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Article
  10. A Bayesian phylodynamic inference framework for single-cell CRISPR/Cas9 lineage tracing barcode data with dependent target sites.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Article
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.

A ZwaansDepartment of Biosystems Science and Engineering, ETH Zurich, Zurich, Switzerland.ORCID 0000-0001-9175-8738
S SeidelDepartment of Biosystems Science and Engineering, ETH Zurich, Zurich, Switzerland.ORCID 0000-0002-4484-9888
M ManceauDepartment of Biosystems Science and Engineering, ETH Zurich, Zurich, Switzerland.ORCID 0000-0001-7368-718X
T StadlerDepartment of Biosystems Science and Engineering, ETH Zurich, Zurich, Switzerland.ORCID 0000-0001-6431-535X

Funding

European Research Council
6 · The paper itself

Abstract

Analysing single-cell lineage relationships of an organism is crucial towards understanding the fundamental cellular dynamics that drive development. Clustered regularly interspaced short palindromic repeats (CRISPR)-based dynamic lineage tracing relies on recent advances in genome editing and sequencing technologies to generate inheritable, evolving genetic barcode sequences that enable reconstruction of such cell lineage trees, also referred to as phylogenetic trees. Recent work generated custom computational strategies to produce robust tree estimates from such data. We further capitalize on these advancements and introduce GESTALT analysis using Bayesian inference (GABI), which extends the analysis of genome editing of synthetic target arrays for lineage tracing (GESTALT) data to a fully integrated Bayesian phylogenetic inference framework in software BEAST 2. This implementation allows users to represent the uncertainty in reconstructed trees and enables their scaling in absolute time. Furthermore, based on such time-scaled lineage trees, the underlying processes of growth, differentiation and apoptosis are quantified through so-called phylodynamic inference, typically relying on a birth-death or coalescent model. After validating its implementation, we demonstrate that our methodology results in robust estimates of growth dynamics characteristic of early

Indexed as

Cell LineageCRISPR-Cas SystemsDNA Barcoding, TaxonomicPhylogenySingle-Cell AnalysisZebrafishAnimalsBayes TheoremSoftwareBEAST 2CRISPRDanio reriolineage tracingphylodynamicssingle-cell

Identifiers

PMID39976408
PMCPMC11867110

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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.