Evidence map›Paper›PMID 42130939›Full record

ArticlePatterns (New York, N.Y.)2026

VoxelCoder: Classification of human cellular phenotypes via autoencoder batch alignment and hyperdimensional representation of cytometry data.

Benjamin S Mashford, Timothy Hewitt, Maryam May, Zixin Zhuang, Akshat Jain, Koula E M Diamand, Fei-Ju Li, Kristy Kwong, Stuart H Read, Ainsley R Davies and 2 more

Abstract read
In one paragraph

Article in Patterns (New York, N.Y.), 2026. 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

12 authors.

Benjamin S MashfordThe John Curtin School of Medical Research, The Australian National University, Canberra, ACT, Australia.
Timothy HewittThe John Curtin School of Medical Research, The Australian National University, Canberra, ACT, Australia.
Maryam MayThe John Curtin School of Medical Research, The Australian National University, Canberra, ACT, Australia.
Zixin ZhuangComputational Science Cluster, School of Computing, College of Systems and Society, The Australian National University, Canberra, ACT, Australia.
Akshat JainComputational Science Cluster, School of Computing, College of Systems and Society, The Australian National University, Canberra, ACT, Australia.
Koula E M DiamandAustralian Phenomics Facility, The Australian National University, Canberra, ACT, Australia.
Fei-Ju LiAustralian Phenomics Facility, The Australian National University, Canberra, ACT, Australia.
Kristy KwongAustralian Phenomics Facility, The Australian National University, Canberra, ACT, Australia.
Stuart H ReadAustralian Phenomics Facility, The Australian National University, Canberra, ACT, Australia.
Ainsley R DaviesAustralian Phenomics Facility, The Australian National University, Canberra, ACT, Australia.
Dillon HammillThe John Curtin School of Medical Research, The Australian National University, Canberra, ACT, Australia.
T Daniel AndrewsThe John Curtin School of Medical Research, The Australian National University, Canberra, ACT, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Technical variations in sample processing and instrument calibration, known as batch effects, can obscure true biological signals in cytometry data, impeding the integration of large-scale datasets. We present an autoencoder neural network approach that achieves batch correction comparable to that in existing methods while better preserving biological variation. Following alignment, cellular datasets are projected into a hyperdimensional voxel space that maintains interpretable marker-based features without requiring abstract latent dimensions, ensuring that identified cell populations remain fully interpretable. We benchmark this approach using a purpose-generated mouse splenocyte dataset with synthetic batch effects, demonstrating superior biological signal preservation compared to existing tools. Applied to clinical datasets, our method enables identification of cellular phenotypes associated with cytomegalovirus serostatus and COVID-19/sepsis discrimination, outperforming alternative approaches in downstream classification tasks. This framework addresses key technical limitations in integrating multi-batch cytometry datasets and provides a foundation for machine-learning applications in cytometry-based diagnostics.

Indexed as

bioinformaticscytometrymachine learning

Identifiers

PMID42130939
PMCPMC13161691

What Socratic 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 Socratic graph.