Challenges in unsupervised clustering of single-cell RNA-seq data
By Vladimir Yu. Kiselev, Tallulah S. Andrews, Martin Hemberg. 2019
1,049 citations recorded by the source corpus.
Subfields: Immunology, Molecular Biology
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In Immunology
In Molecular Biology
- Pavlin Gregor Policar
- Martin Stražar
- Blaz Zupan
- Caleb A. Lareau
- Aleksandr Ianevski
- Miguel Andrade
- Anil K. Giri
- Tero Aittokallio
Citations in the corpus
- openTSNE: a modular Python library for t-SNE dimensionality reduction and embedding (2019, methodology): “We preprocess the data using the standard single-cell analysis pipeline (Kiselev, Andrews, and Hemberg 2019) and extract the top 50 principal components.”
- Fully-automated and ultra-fast cell-type identification using specific marker combinations from single-cell transcriptomic data (2022, methodology): “Identi fi cation of cell populations often relies on unsupervised clustering of cells based on their transcriptomic pro fi les, followed by cluster annotation using marker genes that are differentially-expressed between the clusters 14,15 .”
- Identifying phenotype-associated subpopulations by integrating bulk and single-cell sequencing data (2021, neutral): “One of the advantages is that Scissor does not require any unsupervised clustering on single-cell data, which avoids subjective decisions of cell cluster numbers or clustering resolution 47 .”
- Assessment of computational methods for the analysis of single-cell ATAC-seq data (2019, methodology): “Clustering results were evaluated by three commonly used metrics: adjusted random index (ARI), adjusted mutual information (AMI) and homogeneity when a gold standard solution was available (known labels for the simulation data and FACS-sorted cell populations or known tissues for the real datasets).”