Evidence map›Paper›PMID 42412792›Full record

ArticleBioinformatics (Oxford, England)2026

LAML-Pro: joint maximum likelihood inference of cell genotypes and cell lineage trees.

Gillian Chu, Henri Schmidt, Benjamin J Raphael

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Gillian ChuDepartment of Computer Science, Princeton University, Princeton, NJ 08540, United States.ORCID 0000-0003-2205-730X
Henri SchmidtDepartment of Computer Science, Princeton University, Princeton, NJ 08540, United States.
Benjamin J RaphaelDepartment of Computer Science, Princeton University, Princeton, NJ 08540, United States.

Funding

Comprehensive and Robust Tools for Analysis of Tumor Heterogeneity and EvolutionU24CA248453 · NCI · PRINCETON UNIVERSITY · PI Benjamin Raphael · 2020 to 2026
$4.7M
Pathway, Network and Spatiotemporal Integration of Cancer Genomics DataU24CA264027 · NCI · PRINCETON UNIVERSITY · PI RAPHAEL, BENJAMIN, YEH, JEN JEN · 2021 to 2025
$1.5M
Chan Zuckerberg Initiative Donor-Advised Fund 2024-345885National Science Foundation Graduate Research Fellowship Program #2039656NCI NIH HHS U24 CA248453NCI NIH HHS U24CA248453NCI NIH HHS U24 CA264027NCI NIH HHS U24CA264027Princeton Catalysis InitiativeSilicon Valley Community Foundation
6 · The paper itself

Abstract

motivationRecent dynamic lineage tracing technologies use genome editing to induce heritable mutations, or edits, that accumulate across successive cell divisions. These edits are measured using single-cell sequencing or imaging, providing data to reconstruct cell lineages at single-cell resolution. Current computational approaches to infer cell lineage trees, or phylogenies, from these data perform two separate steps: (i) Identify each cell's edits (genotype) from the raw sequencing or imaging data; (ii) Infer a cell lineage tree from the cell genotypes. However, genotyping cells is an inexact process and genotype errors can yield an inaccurate lineage tree. For example, using fluorescence based-imaging to measure edits results in a high fraction (≈25%-50%) of uncertain or erroneous genotypes.

resultsWe introduce Lineage Analysis via Maximum Likelihood with PRobabilistic Observations (LAML-Pro), an algorithm that jointly infers cell genotypes and a cell lineage tree. LAML-Pro is based on the Probabilistic Mixed-type Missing Observation (PMMO) model, which we derive to describe both the genome editing and genotype observation processes. LAML-Pro constructs lineage trees from thousands of cells in under an hour by leveraging the sparsity of transitions under the PMMO model. On simulated data, we demonstrate that LAML-Pro corrects genotype errors and infers substantially more accurate trees than existing methods which are vulnerable to genotype errors. Applied to data from two recent imaging-based lineage tracing systems, LAML-Pro reduces genotype errors by 5-fold and produces more spatially coherent lineage trees compared to existing methods. AVAILABILITY AND IMPLEMENTATION: LAML-Pro is implemented in C++ and is available as both a command-line interface and as a Python library at: github.com/raphael-group/LAML-Pro.

Indexed as

AlgorithmsCell LineageComputational BiologyGenotypeGene EditingLikelihood FunctionsPhylogenySingle-Cell Analysis

Identifiers

PMID42412792
PMCPMC13341131

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.