Comprehensive generation, visualization, and reporting of quality control metrics for single-cell RNA sequencing data
Rui Hong,
Yusuke Koga,
Shruthi Bandyadka,
Anastasia Leshchyk,
Yichen Wang,
Vidya Akavoor,
Xinyun Cao,
Irzam Sarfraz,
Zhe Wang,
Salam Alabdullatif,
Frederick Jansen,
Masanao Yajima,
W. Evan Johnson and
Joshua D. Campbell ()
Additional contact information
Rui Hong: Bioinformatics Program, Boston University
Yusuke Koga: Bioinformatics Program, Boston University
Shruthi Bandyadka: Bioinformatics Program, Boston University
Anastasia Leshchyk: Bioinformatics Program, Boston University
Yichen Wang: Section of Computational Biomedicine, Boston University School of Medicine
Vidya Akavoor: Section of Computational Biomedicine, Boston University School of Medicine
Xinyun Cao: Software & Application Innovation Lab, Rafik B. Hariri Institute for Computing and Computational Science and Engineering
Irzam Sarfraz: Section of Computational Biomedicine, Boston University School of Medicine
Zhe Wang: Bioinformatics Program, Boston University
Salam Alabdullatif: Section of Computational Biomedicine, Boston University School of Medicine
Frederick Jansen: Software & Application Innovation Lab, Rafik B. Hariri Institute for Computing and Computational Science and Engineering
Masanao Yajima: Boston University
W. Evan Johnson: Bioinformatics Program, Boston University
Joshua D. Campbell: Bioinformatics Program, Boston University
Nature Communications, 2022, vol. 13, issue 1, 1-9
Abstract:
Abstract Single-cell RNA sequencing (scRNA-seq) can be used to gain insights into cellular heterogeneity within complex tissues. However, various technical artifacts can be present in scRNA-seq data and should be assessed before performing downstream analyses. While several tools have been developed to perform individual quality control (QC) tasks, they are scattered in different packages across several programming environments. Here, to streamline the process of generating and visualizing QC metrics for scRNA-seq data, we built the SCTK-QC pipeline within the singleCellTK R package. The SCTK-QC workflow can import data from several single-cell platforms and preprocessing tools and includes steps for empty droplet detection, generation of standard QC metrics, prediction of doublets, and estimation of ambient RNA. It can run on the command line, within the R console, on the cloud platform or with an interactive graphical user interface. Overall, the SCTK-QC pipeline streamlines and standardizes the process of performing QC for scRNA-seq data.
Date: 2022
References: View references in EconPapers View complete reference list from CitEc
Citations:
Downloads: (external link)
https://www.nature.com/articles/s41467-022-29212-9 Abstract (text/html)
Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.
Export reference: BibTeX
RIS (EndNote, ProCite, RefMan)
HTML/Text
Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-29212-9
Ordering information: This journal article can be ordered from
https://www.nature.com/ncomms/
DOI: 10.1038/s41467-022-29212-9
Access Statistics for this article
Nature Communications is currently edited by Nathalie Le Bot, Enda Bergin and Fiona Gillespie
More articles in Nature Communications from Nature
Bibliographic data for series maintained by Sonal Shukla () and Springer Nature Abstracting and Indexing ().