New computational method unravels single-cell data from multiple people

Published this week in Nature Methods, the software could increase efficiency of single-cell experiments, assisting research into transplants, personalised medicine and malaria.

Single-cell RNA sequencing (RNAseq) can reveal exactly which genes are switched on in each individual cell, revealing cell types and what they do. Pooling multiple people's cells into a single cell RNAseq experiment helps to identify how different genomes affect this gene expression. However it is essential to be able to separate the resulting data by individual, which can be very difficult.

The authors tested Souporcell* against three other computational methods using placental cells, pluripotent stem cell lines** and malaria parasites.

Haynes Heaton, the first author from the Wellcome Sanger Institute, said: "Our method, called Souporcell, is able to separate mixtures of individuals' cells in scRNAseq experiments without knowing each individual's full genome sequence beforehand, unlike previous methods. One of the key features of the method is that it estimates the amount of background RNA from dead cells, which is often referred to as the soup. This then allows the removal of that source of noise, and hence the name Souporcell."

Being able to combine the cells into a single experiment increases the accuracy, enabling more information to be found, and also reduces the cost of these experiments.

Dr Martin Hemberg, a senior author from the Wellcome Sanger Institute, said: "The exact genetic sequence of each person can affect their response to infections, or to drug treatments. The new method enables single cell expression data from multiple people to be analysed, to show links between genotype and phenotype, in diseases and in the presence of drugs. This will have implications for personalised medicine."

In addition, some samples inherently have a mix of cells with different genomes, including samples from transplant patients who have their original cells and cells from the donor, or populations of parasites, such as malaria, from an infected individual.

Dr Mara Lawniczak, a senior author from the Wellcome Sanger Institute, said: "This method is helping us understand malaria. People get infected with multiple strains of malaria at once, but we don't know how these strains are competing with each other to reproduce. To even ask the question we have to be able to split out cells of different malaria strains, and Souporcell is enabling this."