Evidence map›Paper›PMID 40287006›Full record

ArticleExperimental hematology2025

C-COUNT: a convolutional neural network-based tool for automated scoring of erythroid colonies.

Rui Li, Ashley Winward, Logan R Lalonde, Daniel Hidalgo, John P Sardella, Yung Hwang, Aishwarya Swaminathan, Sean Thackeray, Kai Hu, Lihua Julie Zhu and 1 more

Abstract read
In one paragraph

Article in Experimental hematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Rui LiDepartment of Molecular, Cell and Cancer Biology, UMass Chan Medical School, Worcester, Massachusetts.
Ashley WinwardDepartment of Molecular, Cell and Cancer Biology, UMass Chan Medical School, Worcester, Massachusetts.
Logan R LalondeDepartment of Molecular, Cell and Cancer Biology, UMass Chan Medical School, Worcester, Massachusetts.
Daniel HidalgoDepartment of Molecular, Cell and Cancer Biology, UMass Chan Medical School, Worcester, Massachusetts.
John P SardellaDepartment of Molecular, Cell and Cancer Biology, UMass Chan Medical School, Worcester, Massachusetts.
Yung HwangDepartment of Molecular, Cell and Cancer Biology, UMass Chan Medical School, Worcester, Massachusetts.
Aishwarya SwaminathanDepartment of Molecular, Cell and Cancer Biology, UMass Chan Medical School, Worcester, Massachusetts.
Sean ThackerayDepartment of Molecular, Cell and Cancer Biology, UMass Chan Medical School, Worcester, Massachusetts.
Kai HuDepartment of Molecular, Cell and Cancer Biology, UMass Chan Medical School, Worcester, Massachusetts.
Lihua Julie ZhuDepartment of Molecular, Cell and Cancer Biology, UMass Chan Medical School, Worcester, Massachusetts. Electronic address: Julie.Zhu@umassmed.edu.
Merav SocolovskyDepartment of Molecular, Cell and Cancer Biology, UMass Chan Medical School, Worcester, Massachusetts. Electronic address: Merav.Socolovsky@umassmed.edu.

Funding

The DNA damage response of fast-cycling erythroblastsR01DK130498 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI SCULLY, RALPH, SOCOLOVSKY, MERAV · 2021 to 2025
$2.9M
Specialized cell cycles in early erythropoiesisR01DK120639 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI SOCOLOVSKY, MERAV · 2019 to 2023
$2.2M
EpoR & Stat5 regulation of ribosome biogenesis and protein synthesis in erythropoiesisR01DK136321 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Merav Socolovsky · 2023 to 2026
$2.0M
BD FACSAriaTM Fusion Fluoresence-Activated Cell SorterS10OD028576 · OD · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI SCHRADER, CAROL E · 2020 to 2020
$565k
NIDDK NIH HHS R01 DK120639NIDDK NIH HHS R01 DK130498NIDDK NIH HHS R01 DK136321NIH HHS S10 OD028576
6 · The paper itself

Abstract

Despite advances in flow cytometry and single-cell transcriptomics, colony-formation assays (CFAs) remain an essential component in the evaluation of erythroid and hematopoietic progenitors. These assays provide functional information on progenitor differentiation and proliferative potential, making them a mainstay of hematology research and clinical diagnosis. However, the utility of CFAs is limited by the time-consuming and error-prone manual counting of colonies, which is also prone to bias and inconsistency. Here we present "C-COUNT," a convolutional neural network-based tool that scores the standard colony-forming-unit-erythroid (CFU-e) assay by reliably identifying CFU-e colonies from images collected by automated microscopy and outputs both their number and size. We tested the performance of C-COUNT against three experienced scientists and find that it is equivalent or better in reliably identifying CFU-e colonies on plates that also contain myeloid colonies and other cell aggregates. We further evaluated its performance in the response of CFU-e progenitors to increasing erythropoietin concentrations and to a spectrum of genotoxic agents. We provide the C-COUNT code, a Docker image, a trained model, and training data set to facilitate its download, usage, and model refinement in other laboratories. The C-COUNT tool transforms the traditional CFU-e CFA into a rigorous and efficient assay with potential applications in high-throughput screens for novel erythropoietic factors and therapeutic agents.

Indexed as

Colony-Forming Units AssayErythroid CellsErythroid Precursor CellsNeural Networks, ComputerAnimalsConvolutional Neural NetworksErythropoietinMiceErythropoietin

Identifiers

PMID40287006
PMCPMC12261521

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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.