scholarly journals Transformation and Preprocessing of Single-Cell RNA-Seq Data

2021 ◽  
Author(s):  
Constantin Ahlmann-Eltze ◽  
Wolfgang Huber

The count table, a numeric matrix of genes × cells, is a basic input data structure in the analysis of single-cell RNA-seq data. A common preprocessing step is to adjust the counts for variable sampling efficiency and to transform them so that the variance is similar across the dynamic range. These steps are intended to make subsequent application of generic statistical methods more palatable. Here, we describe three transformations (based on the delta method, model residuals, or inferred latent expression state) and compare their strengths and weaknesses. We conclude with an outlook on future needs for the development of transformations for single-cell count data.

2021 ◽  
Author(s):  
Lin Di ◽  
Bo Liu ◽  
Yuzhu Lyu ◽  
Shihui Zhao ◽  
Yuhong Pang ◽  
...  

Many single cell RNA-seq applications aim to probe a wide dynamic range of gene expression, but most of them are still challenging to accurately quantify low-aboundance transcripts. Based on our previous finding that Tn5 transposase can directly cut-and-tag DNA/RNA hetero-duplexes, we present SHERRY2, an optimized protocol for sequencing transcriptomes of single cells or single nuclei. SHERRY2 is robust and scalable, and it has higher sensitivity and more uniform coverage in comparison with prevalent scRNA-seq methods. With throughput of a few thousand cells per batch, SHERRY2 can reveal the subtle transcriptomic differences between cells and facilitate important biological discoveries.


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