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STACAS: Sub-Type Anchor Correction for Alignment in Seurat to integrate single-cell RNA-seq data

SUMMARY: STACAS is a computational method for the identification of integration anchors in the Seurat environment, optimized for the integration of single-cell (sc) RNA-seq datasets that share only a subset of cell types. We demonstrate that by (i) correcting batch effects while preserving relevant...

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Detalles Bibliográficos
Autores principales: Andreatta, Massimo, Carmona, Santiago J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8098019/
https://www.ncbi.nlm.nih.gov/pubmed/32845323
http://dx.doi.org/10.1093/bioinformatics/btaa755
Descripción
Sumario:SUMMARY: STACAS is a computational method for the identification of integration anchors in the Seurat environment, optimized for the integration of single-cell (sc) RNA-seq datasets that share only a subset of cell types. We demonstrate that by (i) correcting batch effects while preserving relevant biological variability across datasets, (ii) filtering aberrant integration anchors with a quantitative distance measure and (iii) constructing optimal guide trees for integration, STACAS can accurately align scRNA-seq datasets composed of only partially overlapping cell populations. AVAILABILITY AND IMPLEMENTATION: Source code and R package available at https://github.com/carmonalab/STACAS; Docker image available at https://hub.docker.com/repository/docker/mandrea1/stacas_demo.