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Related Concept Videos

RNA-seq03:21

RNA-seq

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RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
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ScInfeR: an efficient method for annotating cell types and sub-types in single-cell RNA-seq, ATAC-seq, and spatial

Asish Kumar Swain1, Rajveer Singh Shekhawat1, Pankaj Yadav1,2

  • 1Department of Bioscience and Bioengineering, Indian Institute of Technology (IIT), N.H. 62, Nagaur Road, Karwar, Jodhpur 342030, Rajasthan, India.

Briefings in Bioinformatics
|June 5, 2025
PubMed
Summary

ScInfeR is a new graph-based method for cell-type annotation in omics data. It integrates single-cell RNA sequencing references and marker sets, improving accuracy across single-cell RNA sequencing, ATAC-sequencing, and spatial transcriptomics datasets.

Keywords:
cell type annotationscATAC-seqscRNA-seqspatial transcriptomics

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Area of Science:

  • Genomics and Bioinformatics
  • Computational Biology
  • Molecular Biology

Background:

  • Cell-type annotation is crucial for single-cell and spatial omics but faces challenges with limited high-quality references and poor performance in existing methods, especially for scATAC-seq and spatial transcriptomics.
  • Current annotation approaches often rely solely on single-cell RNA sequencing (scRNA-seq) references or predefined marker sets, leading to potential bias and usability issues due to data scarcity.

Purpose of the Study:

  • To develop a versatile and accurate graph-based cell-type annotation method, ScInfeR, that overcomes limitations of existing tools by integrating multiple data sources.
  • To enhance cell-type and subtype identification across diverse omics datasets, including scRNA-seq, scATAC-seq, and spatial transcriptomics, while addressing data scarcity and batch effects.

Main Methods:

  • ScInfeR employs a graph-based approach with a hierarchical framework, inspired by graph neural networks, to combine scRNA-seq references and marker sets for annotation.
  • The method is designed to be versatile, incorporating chromatin accessibility data for scATAC-seq and spatial coordinates for spatial transcriptomics, and supports weighted markers for nuanced classification.
  • ScInfeRDB, an accompanying database, provides curated scRNA-seq references and marker sets for 329 cell-types across human and plant tissues.

Main Results:

  • ScInfeR demonstrated superior performance in extensive benchmarking across multiple atlas-scale datasets, outperforming 10 existing tools in over 100 cell-type prediction tasks.
  • The method showed robustness against batch effects commonly found in omics datasets.
  • ScInfeR accurately annotates a broad range of cell-types and subtypes across scRNA-seq, scATAC-seq, and spatial omics data.

Conclusions:

  • ScInfeR offers a robust and accurate solution for cell-type annotation in single-cell and spatial omics, integrating diverse data types effectively.
  • The tool's versatility and performance improvements address key challenges in the field, facilitating broader application of omics data analysis.
  • The public availability of ScInfeR and its database (ScInfeRDB) promotes reproducible research and advances cell-type annotation capabilities in genomics.