Cargando…
SMaSH: a scalable, general marker gene identification framework for single-cell RNA-sequencing
BACKGROUND: Single-cell RNA-sequencing is revolutionising the study of cellular and tissue-wide heterogeneity in a large number of biological scenarios, from highly tissue-specific studies of disease to human-wide cell atlases. A central task in single-cell RNA-sequencing analysis design is the calc...
Autores principales: | Nelson, M. E., Riva, S. G., Cvejic, A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9361618/ https://www.ncbi.nlm.nih.gov/pubmed/35941549 http://dx.doi.org/10.1186/s12859-022-04860-2 |
Ejemplares similares
-
SMaSH: Sample matching using SNPs in humans
por: Westphal, Maximillian, et al.
Publicado: (2019) -
SmashCell: a software framework for the analysis of single-cell amplified genome sequences
por: Harrington, Eoghan D., et al.
Publicado: (2010) -
SMASH: Scalable Method for Analyzing Spatial Heterogeneity of genes in spatial transcriptomics data
por: Seal, Souvik, et al.
Publicado: (2023) -
SMASH: Scalable Method for Analyzing Spatial Heterogeneity of genes in spatial transcriptomics data
por: Seal, Souvik, et al.
Publicado: (2023) -
Study of common-mode noise of the SMA$^{2}$SH-64A preamplifier array
por: Ikeda, H, et al.
Publicado: (1996)