Cell ReportsGenomicsPeer-reviewed journal article
ALS molecular subtypes are a combination of cellular, genetic, and pathological features learned by deep multiomics classifiers
Kathryn O’NeilliD, Regina Shaw, Isobel Bolger, Oliver H. TamiD, Hemali P. PhatnaniiD, Molly HammelliD
Abstract
Amyotrophic Lateral Sclerosis (ALS) is a complex syndrome with multiple genetic causes and wide variation in disease presentation. Despite this general heterogeneity, several common factors have been identified. For example, nearly all patients show pathological accumulations of phosphorylated TDP-43 protein in affected regions of the motor cortex and spinal cord. Moreover, large patient cohort studies have revealed that most patient samples can be grouped into a small number of ALS subtypes, as defined by their transcriptomic profiles. These ALS molecular subtypes can be grouped by whether postmortem motor cortex samples display signatures of: mitochondrial dysfunction and oxidative stress (ALS-Ox), microglial activation and neuroinflammation (ALS-Glia), or dense TDP-43 pathology and associated transposable element de-silencing (ALS-TE). In this study, we have built a deep layer ALS neural network classifier (DANcer) that has learned to accurately assign patient samples to these ALS subtypes, and which can be run on either bulk or single-cell datasets. Upon applying this classifier to an expanded ALS patient cohort from the NYGC ALS Consortium, we show that ALS Molecular Subtypes are robust across clinical centers, with no new subtypes appearing in a cohort that has quadrupled in size. Signatures from two of these molecular subtypes strongly correlate with disease duration: ALS-TE signatures in cortex and ALS-Glia signatures in spinal cord, revealing molecular correlates of clinical features. Finally, we use single nucleus RNA sequencing to reveal the cell type-specific contributions to ALS subtype, as determined by our single-cell classifier (scDANCer). Single-cell transcriptomes reveal that ALS molecular subtypes are recapitulated in neurons and glia, with both ALS-wide shared alterations in each cell type as well as ALS subtype-specific alterations. In summary, ALS molecular subtypes: (1) are robust across large cohorts of sporadic and familial ALS patient samples, (2) represent a combination of cellular, genetic, and pathological features, and (3) correlate with clinical features of ALS. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=148 SRC="FIGDIR/small/603731v1_ufig1.gif" ALT="Figure 1"> View larger version (42K): org.highwire.dtl.DTLVardef@df6e03org.highwire.dtl.DTLVardef@af9beborg.highwire.dtl.DTLVardef@12594f1org.highwire.dtl.DTLVardef@557dae_HPS_FORMAT_FIGEXP M_FIG O_FLOATNOFigure 0:C_FLOATNO Graphical Abstract - ALS molecular subtypes are a combination of cellular, genetic, and pathological features learned by deep multiomics classifiers. C_FIG
- organism: human
- assay: bulk RNA-seq
- assay: scRNA-seq
- research focus: cell type annotation
- research focus: clustering
- research focus: differential expression
- research focus: gene regulatory network inference
- approach: deep learning
- Citations
- 42
- FWCI
- 25.57
- Field percentile
- top 1%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Machine learning evaluation of gene expression-based ALS subtypes across brain and blood tissues
Esteban A. Gómez, Ahmad Al Khleifat, … Alfredo Iacoangeli·bioRxiv·Jun 21, 2026
- Postmortem Cortex Samples Identify Distinct Molecular Subtypes of ALS: Retrotransposon Activation, Oxidative Stress, and Activated Glia
Oliver H. Tam, Nikolay V. Rozhkov, … John Ravits·Cell ReportsPeer-reviewed·Oct 1, 2019
- Multiscale Transcriptomic Architecture of the ALS Motor Cortex
Aadya Goel, Shaojun Pei, Gil Alterovitz·bioRxiv·Oct 30, 2026
- Identification of molecular and clinical ALS subgroups based on TDP-43 loss of function molecular markers from population-based patient-derived iPS motor neurons
T. L. Cheng, shaili tripathi, … Jeffrey D. Rothstein·bioRxiv·Jan 7, 2026
- Predictive Cellular Signatures from Live Human Motor Neurons Distinguish TDP-43 ALS and Enable ALS Subtype Stratification
Julia Kaye, Naufa Amirani, … Steven M. Finkbeiner·bioRxiv·Apr 24, 2026
- A scalable screening platform for phenotypic subtyping of ALS patient-derived fibroblasts
Karl Kumbier, Maike A. Roth, … Steven J. Altschuler·bioRxiv·Sep 27, 2022