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Ning Leng

Publications and source records attributed to Ning Leng.

2 recordsLinked to original sources

SCPattern: A statistical approach to identify and classify expression changes in single cell RNA-seq experiments with ordered conditions

MotivationWith the development of single cell RNA-seq (scRNA-seq) technology, scRNA-seq experiments with ordered conditions (e.g. time-course) are becoming common. Methods developed for analyzing ordered bulk RNA-seq experiments are not applicable to scRNA-seq, since their distributional assumptions are often violated by additional heterogeneities prevalent in scRNA-seq. Here we present SC-Pattern - an empirical Bayes model to characterize genes with expression changes in ordered scRNA-seq experiments. SCPattern utilizes the non-parametrical Kolmogorov-Smirnov statistic, thus it has the flexibility to identify genes with a wide variety of types of changes. Additionally, the Bayes framework allows SCPattern to classify genes into expression patterns with probability estimates.\n\nResultsSimulation results show that SCPattern is well powered for identifying genes with expression changes while the false discovery rate is well controlled. SCPattern is also able to accurately classify these dynamic genes into directional expression patterns. Applied to a scRNA-seq time course dataset studying human embryonic cell differentiation, SCPattern detected a group of important genes that are involved in mesendoderm and definitive endoderm cell fate decisions, positional patterning, and cell cycle.\n\nAvailability and ImplementationThe SCPattern is implemented as an R package along with a user-friendly graphical interface, which are available at:https://github.com/lengning/SCPattern\n\nContact: rstewart@morgridge.org

Bioinformatics

OEFinder: A user interface to identify and visualize ordering effects in single-cell RNA-seq data

A recent paper identified an artifact in multiple single-cell RNA-seq (scRNA-seq) data sets generated by the Fluidigm C1 platform. Specifically, Leng* et al. showed significantly increased gene expression in cells captured from sites with small or large plate output IDs. We refer to this artifact as an ordering effect (OE). Including OE genes in downstream analyses could lead to biased results. To address this problem, we developed a statistical method and software called OEFinder to identify a sorted list of OE genes. OEFinder is available as an R package along with user-friendly graphical interface implementations that allows users to check for potential artifacts in scRNA-seq data generated by the Fluidigm C1 platform.\n\nAvailability and ImplementationOEFinder is freely available at https://github.com/lengning/OEFinder\n\nContactrstewart@morgridge.org

Bioinformatics