HiTSelect

HiTSelect deconvolves and analyzes pooled high-throughput genetic screens from next-generation sequencing readouts to identify screen hits and support downstream functional and network interpretation.


Key Features:

  • Rigorous statistical analysis: Implements statistical modules to identify screen hits and address random noise and statistical biases in high-throughput data.
  • Off-target effect mitigation: Integrates relevant metadata to detect and mitigate off-target effects in genetic screens.
  • Variance control: Controls for variance in gene silencing efficiency and sequencing depth of coverage.
  • Functional and network analysis: Provides downstream analysis to explore biological pathways and interactions implicated by screen hits.

Scientific Applications:

  • Genome-wide RNAi screens: Analysis and hit selection from pooled RNAi screens using next-generation sequencing readouts.
  • CRISPR/Cas9 screens: Analysis and hit selection from pooled CRISPR/Cas9 screens using next-generation sequencing readouts.
  • Gene function elucidation: Identifying genes implicated by screens to infer gene function.
  • Therapeutic target identification: Prioritizing candidate genes for potential therapeutic targeting based on screen results.
  • Biological network exploration: Mapping implicated genes to pathways and interaction networks for systems-level interpretation.

Methodology:

Performs deconvolution of pooled screens from next-generation sequencing, applies statistical hit-calling modules, integrates metadata to mitigate off-target effects, controls for gene silencing efficiency and sequencing depth variance, and conducts downstream functional and network analyses.

Topics

Details

Tool Type:
desktop application
Operating Systems:
Linux, Windows, Mac
Programming Languages:
Java, MATLAB
Added:
8/3/2017
Last Updated:
11/25/2024

Operations

Publications

Diaz AA, Qin H, Ramalho-Santos M, Song JS. HiTSelect: a comprehensive tool for high-complexity-pooled screen analysis. Nucleic Acids Research. 2014;43(3):e16-e16. doi:10.1093/nar/gku1197. PMID:25428347. PMCID:PMC4330337.

Documentation

Links