uncoverappLib
uncoverappLib provides a suite of graphical and statistical tools to support clinical assessment of low coverage regions at the base-pair level.
Key Features:
- Coverage Analysis Module: Provides statistical summary of coverage given a target file or gene names.
- Allele Frequency Calculation Module: Calculates allele frequency (AF) by allele frequency.
- Binomial Distribution Module: Provides binomial distribution analysis as a separate analytical module.
Scientific Applications:
- Clinical Sequence Coverage Assessment: Supports clinical evaluation of low coverage regions in sequencing data at base-pair resolution.
- Targeted Coverage Analysis: Enables coverage analysis using target files or specified gene names for focused genomic regions.
Methodology:
The tool implements graphical and statistical methods through three analysis modules: Coverage analysis, allele frequency calculation, and binomial distribution analysis.
Collections
Details
- License:
- MIT
- Tool Type:
- command-line tool, library
- Operating Systems:
- Linux, Mac, Windows
- Programming Languages:
- R
- Added:
- 8/30/2026
- Last Updated:
- 8/30/2026
Operations
Publications
Documentation
Downloads
- Source codehttps://github.com/Manuelaio/uncoverappLib