Evidence map›Paper›PMID 32343706›Full record

ArticlePLoS computational biology2020

Predicting cell lineages using autoencoders and optimal transport.

Karren Dai Yang, Karthik Damodaran, Saradha Venkatachalapathy, Ali C Soylemezoglu, G V Shivashankar, Caroline Uhler

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
8.6field-weighted citation impact, top 2% of its field
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

22 citing papers in PubMed, 62 citations in OpenAlex.

  1. Review
  2. Article
  3. MultistageOT: Multistage optimal transport infers trajectories from a snapshot of single-cell data.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Debiasing Sinkhorn divergence in optimal transport of cellular dynamics.bioRxiv : the preprint server for biology · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. A genome-wide optical pooled screen reveals regulators of cellular antiviral responses.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  15. Article
  16. Review
  17. SCOT: Single-Cell Multi-Omics Alignment with Optimal Transport.Journal of computational biology : a journal of computational molecular cell biology · 2022
    Article
  18. Article
  19. Article
  20. Data science in cell imaging.Journal of cell science · 2021
    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

6 authors at 3 institutions in 4 countries.

Karren Dai YangInstitute for Data, Systems and Society, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.
Karthik DamodaranMechanobiology Institute, National University of Singapore, Singapore.
Saradha VenkatachalapathyMechanobiology Institute, National University of Singapore, Singapore.ORCID 0000-0002-7639-0506
Ali C SoylemezogluInstitute for Data, Systems and Society, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.ORCID 0000-0002-9338-9232
G V ShivashankarMechanobiology Institute, National University of Singapore, Singapore.ORCID 0000-0002-3445-4567
Caroline UhlerInstitute for Data, Systems and Society, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.ORCID 0000-0002-7008-0216
National University of Singapore · SGMassachusetts Institute of Technology · USETH Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lineage tracing involves the identification of all ancestors and descendants of a given cell, and is an important tool for studying biological processes such as development and disease progression. However, in many settings, controlled time-course experiments are not feasible, for example when working with tissue samples from patients. Here we present ImageAEOT, a computational pipeline based on autoencoders and optimal transport for predicting the lineages of cells using time-labeled datasets from different stages of a cellular process. Given a single-cell image from one of the stages, ImageAEOT generates an artificial lineage of this cell based on the population characteristics of the other stages. These lineages can be used to connect subpopulations of cells through the different stages and identify image-based features and biomarkers underlying the biological process. To validate our method, we apply ImageAEOT to a benchmark task based on nuclear and chromatin images during the activation of fibroblasts by tumor cells in engineered 3D tissues. We further validate ImageAEOT on chromatin images of various breast cancer cell lines and human tissue samples, thereby linking alterations in chromatin condensation patterns to different stages of tumor progression. Our results demonstrate the promise of computational methods based on autoencoding and optimal transport principles for lineage tracing in settings where existing experimental strategies cannot be used.

Indexed as

Cell LineageBreast NeoplasmsCell DifferentiationCell Line, TumorCell NucleusChromatinCoculture TechniquesComputational BiologyFemaleHumansImage Processing, Computer-AssistedReproducibility of ResultsSingle-Cell AnalysisChromatin

Identifiers

PMID32343706
PMCPMC7209334
OpenAlexW3017662469

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.