VeloSim

VeloSim simulates single-cell RNA sequencing (scRNA-seq) data to model gene-expression kinetics along defined cellular trajectories for benchmarking trajectory inference and RNA velocity estimation methods.


Key Features:

  • Trajectory Simulation: Accepts predefined trajectory structures including linear, cycle, and cycle-tree to simulate diverse developmental processes.
  • Gene-Expression Kinetics: Simulates mRNA generation dynamics and produces both unspliced and spliced mRNA count matrices.
  • RNA Velocity Estimation: Computes true RNA velocity measurements along trajectories to indicate direction and speed of cellular transitions.
  • Benchmarking Capability: Generates datasets with varying levels of biological and technical variation for evaluating trajectory inference and RNA velocity methods.
  • Output Annotations: Produces cell pseudo-time annotations alongside count matrices and true RNA velocity measurements.

Scientific Applications:

  • Developmental Dynamics: Study molecular mechanisms driving cellular dynamics during differentiation and development using simulated scRNA-seq data.
  • Method Benchmarking: Benchmark and validate trajectory inference and RNA velocity estimation methods using ground-truth unspliced/spliced matrices, pseudo-time, and true velocities.
  • Algorithm Development: Develop and test algorithms for single-cell genomics, including trajectory reconstruction and velocity-based analyses.

Methodology:

Takes predefined trajectory structures (e.g., linear, cycle, cycle-tree) as input and simulates gene-expression kinetics (mRNA generation) along these paths to output unspliced and spliced mRNA count matrices, cell pseudo-time annotations, and true RNA velocity measurements with varying biological and technical variation.

Topics

Details

Tool Type:
command-line tool, library
Programming Languages:
R
Added:
3/19/2021
Last Updated:
7/7/2021

Operations

Publications

Zhang Z, Zhang X. VeloSim: Simulating single cell gene-expression and RNA velocity. Unknown Journal. 2021. doi:10.1101/2021.01.11.426277.