# VSHunter **Repository Path**: ShixiangWang/VSHunter ## Basic Information - **Project Name**: VSHunter - **Description**: No description available - **Primary Language**: Unknown - **License**: MIT - **Default Branch**: master - **Homepage**: None - **GVP Project**: No ## Statistics - **Stars**: 0 - **Forks**: 0 - **Created**: 2021-08-31 - **Last Updated**: 2024-05-30 ## Categories & Tags **Categories**: Uncategorized **Tags**: None ## README # VSHunter: Capture Variation Signatures from Genomic Data [![GitHub tag](https://img.shields.io/github/tag/ShixiangWang/VSHunter.svg?label=Github)](https://github.com/ShixiangWang/VSHunter) [![lifecycle](https://img.shields.io/badge/lifecycle-retire-orange.svg)](https://www.tidyverse.org/lifecycle/#retire) [![Travis build status](https://travis-ci.org/ShixiangWang/VSHunter.svg?branch=master)](https://travis-ci.org/ShixiangWang/VSHunter) [![codecov](https://codecov.io/gh/ShixiangWang/VSHunter/branch/master/graph/badge.svg)](https://codecov.io/gh/ShixiangWang/VSHunter) [![DOI](https://zenodo.org/badge/153238002.svg)](https://zenodo.org/badge/latestdoi/153238002) **This package retired, users should switch to R package [**sigminer**](https://github.com/ShixiangWang/sigminer)** The goal of VSHunter is to capture variation signature from genomic data. For now, we decode copy number pattern from **absolute copy number profile**. This package collects R code from paper *[Copy number signatures and mutational processes in ovarian carcinoma](https://www.nature.com/articles/s41588-018-0179-8)* and tidy them as a open source R package for bioinformatics community. Before you use this tool, you have to obtain **absolute copy number profile** for samples via software like ABSOLUTE v2, QDNASeq etc.. ## Procedure 1. summarise copy-number profile using a number of different feature distributions: - Sgement size - Breakpoint number (per ten megabases) - change-point copy-number - Breakpoint number (per chromosome arm) - Length of segments with oscillating copy-number 2. apply mixture modelling to breakdown each feature distribution into mixtures of Gaussian or mixtures of Poisson distributions using the flexmix package. 3. generate a sample-by-component matrix representing the sum of posterior probabilities of each copy-number event being assigned to each component. 4. use NMF package to factorise the sample-by-component matrix into a signature-by-sample matrix and component-by signature-matrix. Copy number signature identification, Macintyre, Geoff, et al.(2018) ## Installation You can install UCSCXenaTools from github with: ``` r # install.packages("devtools") devtools::install_github("ShixiangWang/VSHunter", build_vignettes = TRUE) ``` > update features and function will show in vignettes in the future Load package. ``` r library(VSHunter) ``` ## Citation - *Macintyre, Geoff, et al. “Copy number signatures and mutational processes in ovarian carcinoma.” Nature genetics 50.9 (2018): 1262.* If you wanna thank my work for this package, you can also cite (and inlucde link of this package - ): - *Wang, Shixiang, et al. “APOBEC3B and APOBEC mutational signature as potential predictive markers for immunotherapy response in non-small cell lung cancer.” Oncogene (2018).*