Evidence map›Paper›PMID 36947171›Full record

ArticleMolecular biology of the cell2023

Predicting reprogramming-related gene expression from cell morphology in human induced pluripotent stem cells.

Takashi Wakui, Mitsuru Negishi, Yuta Murakami, Shunsuke Tominaga, Yasushi Shiraishi, Anne E Carpenter, Shantanu Singh, Hideo Segawa

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2023. 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
1.8field-weighted citation impact, top 15% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Machine Learning in Stem Cell Research: From Biological Data to Clinical Translation.Computational and structural biotechnology journal · 2026
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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

8 authors at 3 institutions in 2 countries.

Takashi WakuiBio Science & Engineering Laboratories, Fujifilm Corporation, Madison, WI 53711.ORCID 0000-0003-2704-070X
Mitsuru NegishiImaging Technology Center, Fujifilm Corporation, Ashigarakami-gun, Kanagawa 258-0023, Japan.
Yuta MurakamiBio Science & Engineering Laboratories, Fujifilm Corporation, Ashigarakami-gun, Kanagawa 258-0021, Japan.
Shunsuke TominagaImaging Technology Center, Fujifilm Corporation, Ashigarakami-gun, Kanagawa 258-0023, Japan.
Yasushi ShiraishiImaging Technology Center, Fujifilm Corporation, Ashigarakami-gun, Kanagawa 258-0023, Japan.
Anne E CarpenterImaging Platform, Broad Institute of Harvard and MIT, Cambridge, MA 02142.ORCID 0000-0003-1555-8261
Shantanu SinghImaging Platform, Broad Institute of Harvard and MIT, Cambridge, MA 02142.ORCID 0000-0003-3150-3025
Hideo SegawaImaging Technology Center, Fujifilm Corporation, Ashigarakami-gun, Kanagawa 258-0023, Japan.
Fujifilm (Japan) · JPBroad Institute · USFujifilm (United States) · US

Funding

Extracting rich information from biological imagesR35GM122547 · NIGMS · BROAD INSTITUTE, INC. · PI Anne E. Carpenter · 2017 to 2026
$6.2M
NIGMS NIH HHS R35 GM122547
6 · The paper itself

Abstract

Purification is essential before differentiating human induced pluripotent stem cells (hiPSCs) into cells that fully express particular differentiation marker genes. High-quality iPSC clones are typically purified through gene expression profiling or visual inspection of the cell morphology; however, the relationship between the two methods remains unclear. We investigated the relationship between gene expression levels and morphology by analyzing live-cell, phase-contrast images and mRNA profiles collected during the purification process. We employed these data and an unsupervised image feature extraction method to build a model that predicts gene expression levels from morphology. As a benchmark, it was confirmed that the method can predict the gene expression levels from tissue images for cancer genes, performing as well as state-of-the-art methods. We then applied the method to iPSCs and identified two genes that are well predicted from cell morphology. Although strong batch (or possibly donor) effects resulting from the reprogramming process preclude the ability to use the same model to predict across batches, prediction within a reprogramming batch is sufficiently robust to provide a practical approach for estimating expression levels of a few genes and monitoring the purification process.

Indexed as

Induced Pluripotent Stem CellsCell DifferentiationCellular ReprogrammingGene ExpressionGene Expression ProfilingHumans

Identifiers

PMID36947171
PMCPMC10162412
OpenAlexW4353020443

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.