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Biology subjects

Richard, A. C.

Publications and source records attributed to Richard, A. C..

2 recordsLinked to original sources

Robust expression variability testing reveals heterogeneous T cell responses

Cell-to-cell transcriptional variability in otherwise homogeneous cell populations plays a crucial role in tissue function and development. Single-cell RNA sequencing can characterise this variability in a transcriptome-wide manner. However, technical variation and the confounding between variability and mean expression estimates hinders meaningful comparison of expression variability between cell populations. To address this problem, we introduce a novel analysis approach that extends the BASiCS statistical framework to derive a residual measure of variability that is not confounded by mean expression. Moreover, we introduce a new and robust procedure for quantifying technical noise in experiments where technical spike-in molecules are not available. We illustrate how our method provides biological insight into the dynamics of cell-to-cell expression variability, highlighting a synchronisation of the translational machinery in immune cells upon activation. Additionally, our approach identifies new patterns of variability across CD4+ T cell differentiation.

bioinformatics

Detection and removal of barcode swapping in single-cell RNA-seq data

Barcode swapping results in the mislabeling of sequencing reads between multiplexed samples on the new patterned flow cell Illumina sequencing machines. This may compromise the validity of numerous genomic assays, especially for single-cell studies where many samples are routinely multiplexed together. The severity and consequences of barcode swapping for single-cell transcriptomic studies remain poorly understood. We have used two statistical approaches to robustly quantify the fraction of swapped reads in each of two plate-based single-cell RNA sequencing datasets. We found that approximately 2.5% of reads were mislabeled between samples on the HiSeq 4000 machine, which is lower than previous reports. We observed no correlation between the swapped fraction of reads and the concentration of free barcode across plates. Furthermore, we have demonstrated that barcode swapping may generate complex but artefactual cell libraries in droplet-based single-cell RNA sequencing studies. To eliminate these artefacts, we have developed an algorithm to exclude individual molecules that have swapped between samples in 10X Genomics experiments, exploiting the combinatorial complexity present in the data. This permits the continued use of cutting-edge sequencing machines for droplet-based experiments while avoiding the confounding effects of barcode swapping.

genomics