SIMS: A deep-learning label transfer tool for single-cell RNA sequencing analysis DOI Creative Commons
Jesus Gonzalez-Ferrer, Julian Lehrer, Ash O’Farrell

et al.

Cell Genomics, Journal Year: 2024, Volume and Issue: 4(6), P. 100581 - 100581

Published: May 31, 2024

Cell atlases serve as vital references for automating cell labeling in new samples, yet existing classification algorithms struggle with accuracy. Here we introduce SIMS (scalable, interpretable machine learning single cell), a low-code data-efficient pipeline single-cell RNA classification. We benchmark against datasets from different tissues and species. demonstrate SIMS's efficacy classifying cells the brain, achieving high accuracy even small training sets (<3,500 cells) across samples. accurately predicts neuronal subtypes developing shedding light on genetic changes during differentiation postmitotic fate refinement. Finally, apply to of cortical organoids predict identities uncover variations between lines. identifies cell-line differences misannotated lineages human derived pluripotent stem Altogether, show that is versatile robust tool cell-type datasets.

Language: Английский

Integrated analysis of molecular atlases unveils modules driving developmental cell subtype specification in the human cortex DOI Creative Commons
Patricia R. Nano, Elisa Fazzari, Daria Azizad

et al.

Nature Neuroscience, Journal Year: 2025, Volume and Issue: unknown

Published: April 21, 2025

Human brain development requires generating diverse cell types, a process explored by single-cell transcriptomics. Through parallel meta-analyses of the human cortex in (seven datasets) and adulthood (16 datasets), we generated over 500 gene co-expression networks that can describe mechanisms cortical development, centering on peak stages neurogenesis. These meta-modules show dynamic subtype specificities throughout with several developmental displaying spatiotemporal expression patterns allude to potential roles fate specification. We validated these modules primary tissues. include meta-module 20, module elevated FEZF2+ deep layer neurons includes TSHZ3, transcription factor associated neurodevelopmental disorders. chimeroid experiments both FEZF2 TSHZ3 are required drive 20 activity neuron specification but through distinct modalities. studies demonstrate how meta-atlases engender further mechanistic analyses

Language: Английский

Citations

1

Development and Application of Brain Region–Specific Organoids for Investigating Psychiatric Disorders DOI Creative Commons
Zhijian Zhang, Xin Wang, Sean S. Park

et al.

Biological Psychiatry, Journal Year: 2022, Volume and Issue: 93(7), P. 594 - 605

Published: Dec. 24, 2022

Language: Английский

Citations

33

Stem Cell–Based Organoid Models of Neurodevelopmental Disorders DOI
Lu Wang,

Charlotte Owusu-Hammond,

David Sievert

et al.

Biological Psychiatry, Journal Year: 2023, Volume and Issue: 93(7), P. 622 - 631

Published: Jan. 25, 2023

Language: Английский

Citations

20

Development and evolution of the primate neocortex from a progenitor cell perspective DOI
Colette Dehay, Wieland Β. Huttner

Development, Journal Year: 2024, Volume and Issue: 151(4)

Published: Feb. 15, 2024

ABSTRACT The generation of neurons in the developing neocortex is a major determinant size. Crucially, increase cortical neuron numbers primate lineage, notably upper-layer neurons, contributes to increased cognitive abilities. Here, we review evolutionary changes affecting apical progenitors ventricular zone and focus on key germinal constituting foundation neocortical neurogenesis primates, outer subventricular (OSVZ). We summarize characteristic features OSVZ its stem cell type, basal (or outer) radial glia. Next, concentrate primate-specific human-specific genes, expressed OSVZ-progenitors, ability which amplify these by targeting regulation cycle ultimately underlies neurons. Finally, address likely differences development between present-day humans Neanderthals that are based amino acid substitutions proteins operating progenitors.

Language: Английский

Citations

7

SIMS: A deep-learning label transfer tool for single-cell RNA sequencing analysis DOI Creative Commons
Jesus Gonzalez-Ferrer, Julian Lehrer, Ash O’Farrell

et al.

Cell Genomics, Journal Year: 2024, Volume and Issue: 4(6), P. 100581 - 100581

Published: May 31, 2024

Cell atlases serve as vital references for automating cell labeling in new samples, yet existing classification algorithms struggle with accuracy. Here we introduce SIMS (scalable, interpretable machine learning single cell), a low-code data-efficient pipeline single-cell RNA classification. We benchmark against datasets from different tissues and species. demonstrate SIMS's efficacy classifying cells the brain, achieving high accuracy even small training sets (<3,500 cells) across samples. accurately predicts neuronal subtypes developing shedding light on genetic changes during differentiation postmitotic fate refinement. Finally, apply to of cortical organoids predict identities uncover variations between lines. identifies cell-line differences misannotated lineages human derived pluripotent stem Altogether, show that is versatile robust tool cell-type datasets.

Language: Английский

Citations

7