Solo: Doublet Identification in Single-Cell RNA-Seq via Semi-Supervised Deep Learning

Nicholas Bernstein, Nicole L. Fong, Irene Lam, Margaret A. Roy, David G. Hendrickson, David R. Kelley

Cell Systems 2020 article cited by 275

importance 5/10 solved Single-cell and spatial transcriptomics single-cell genomics stage: research open-source model

In single-cell RNA sequencing, 'doublets' (two or more cells sharing one barcode) violate the technology's premise and can lead to incorrect biological inferences.

Doublet contamination can invalidate downstream conclusions in single-cell research.

Solo embeds cells unsupervised with a variational autoencoder, then appends a feed-forward neural network layer trained to distinguish simulated doublets from real data, identifying doublets more accurately than existing methods.

Claims greater accuracy than existing methods; no quantitative numbers stated in abstract

Freely released tool that can be combined with experimental methods to purify scRNA-seq data.

Venue Cell Systems
Published 2020
Work type article
Authors Nicholas Bernstein, Nicole L. Fong, Irene Lam, Margaret A. Roy, David G. Hendrickson, David R. Kelley
Citations 275 (OpenAlex, at import time)
References 44
Model or method Variational autoencoder with feed-forward neural network classifier
Organization Calico (per GitHub URL calico/solo)
Primary source https://doi.org/10.1016/j.cels.2020.05.010
Open access hybrid
Keywords doublets, scRNA-seq, semi-supervised deep learning, variational autoencoder, data purification
5 / 10

real but narrower advance

Doublet contamination can invalidate single-cell sequencing conclusions; a useful methodological fix for a widely used technology, but no scale stated.

Basis: inferred. Judged from the source text, which gives no explicit scale. Stated scale: not stated in source. Method and limits.

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