From: Liver in infections: a single-cell and spatial transcriptomics perspective
Technologies | Molecular layer | Application | Ref. |
---|---|---|---|
ScRNA-seq | Transcriptomic | Applicable for fresh tissue samples only and artificial transcriptional stress responses | [69] |
SnRNA-seq | Transcriptomic | Application to fresh and frozen samples, particularly those that are difficult to dissociate into single-cell suspensions. Can provide data on difficult to isolate cells with some loss of transcriptional depth and the cytoplasmic RNA fraction | [16] |
Spatial transcriptomics | Transcriptomic | Used to eliminate dependency on landmark genes and adherent cells, and provide spatial annotation of structures | |
Sc ATAC-seq | Epigenetic | Unbiased detection of epigenetic landscape across the human genome. Capture of early lineage-determining epigenetic features may allow for a higher resolution when identifying cell subsets than with transcriptomic data | [62] |
Single-cell immune profiling | Transcriptomic and TCR sequencing | Enables annotation of invariant T-cells, tracking the expansion of T- and B-cells and the linking of antigen receptor sequences to lymphocyte transcriptome | [190] |
Sc MT-seq | Multiomic: epigenetic and transcriptomic | Used to detect transcriptome, methylome, and single nucleotide polymorphism information within single cells to dissect the mechanisms of epigenetic gene regulation | |
Sc CITE-seq | Multiomic: transcriptomic and proteomic | Used to provide detailed characterization of cellular phenotypes and be readily scale as the throughput of single-cell sequencing approaches increase | [65] |
Single-microbe genomics | Genomic | Contribute high-throughput culture-free capabilities to investigate genomic blueprints of complex microbial communities with single-microbe resolution | [67] |