Doublets formed during single-cell RNA sequencing (scRNA-seq) severely affect downstream studies, such as differentially expressed gene analysis and cell trajectory inference, and limit the cellular throughput of scRNA-seq. Several doublet detection...
Read More »SAMStat 2 – quality control for next generation sequencing data
SAMStat is an efficient program to extract quality control metrics from fastq and SAM/BAM files. A distinguishing feature is that it displays sequence composition, base quality composition and...
Read More »COPILOT – fast scRNA-seq raw data processing using scKB and non-arbitrary quality control
Researchers from Humboldt Universität zu Berlin describe a protocol to perform fast and non-arbitrary quality control of single-cell RNA sequencing...
Read More »popsicleR – an R package for pre-processing and quality control analysis of single cell RNA-seq data
The advent of single-cell sequencing is providing unprecedented opportunities to disentangle tissue complexity and investigate cell identities and functions. However, the analysis of single cell data is a challenging, multi-step process that requires both...
Read More »Quick determination of RNA-Seq strandedness
Quality control checks are the first step in RNA-Sequencing analysis, which enable the identification of common issues that occur in the sequenced reads. Checks for sequence quality, contamination...
Read More »miQC – An adaptive probabilistic framework for quality control of single-cell RNA-sequencing data
Researchers have developed a data-driven QC metric that jointly models both the proportion of reads mapping to mtDNA genes and the number of...
Read More »DropletQC – improved identification of empty droplets and damaged cells in single-cell RNA-seq data
Advances in droplet-based single cell RNA-sequencing (scRNA-seq) have dramatically increased throughput, allowing tens of thousands of cells to be routinely sequenced in a single experiment...
Read More »RNA2HLA – HLA-based quality control of RNA-Seq datasets
RNA-sequencing (RNA-seq) is a widely used approach for accessing the transcriptome in biomedical research. Studies frequently include multiple samples taken from the same individual...
Read More »The case for using mapped exonic non-duplicate reads when reporting RNA-sequencing depth
The reproducibility of gene expression measured by RNA sequencing (RNA-Seq) is dependent on the sequencing depth. While unmapped or non-exonic reads do not contribute to gene expression quantification, duplicate reads contribute to the quantification...
Read More »The spatial RNA integrity number assay for in situ evaluation of transcriptome quality
The RNA integrity number (RIN) is a frequently used quality metric to assess the completeness of rRNA, as a proxy for the corresponding mRNA in a tissue...
Read More »