SNPhood

DOI: 10.18129/B9.bioc.SNPhood    

This package is for version 3.7 of Bioconductor; for the stable, up-to-date release version, see SNPhood.

SNPhood: Investigate, quantify and visualise the epigenomic neighbourhood of SNPs using NGS data

Bioconductor version: 3.7

To date, thousands of single nucleotide polymorphisms (SNPs) have been found to be associated with complex traits and diseases. However, the vast majority of these disease-associated SNPs lie in the non-coding part of the genome, and are likely to affect regulatory elements, such as enhancers and promoters, rather than function of a protein. Thus, to understand the molecular mechanisms underlying genetic traits and diseases, it becomes increasingly important to study the effect of a SNP on nearby molecular traits such as chromatin environment or transcription factor (TF) binding. Towards this aim, we developed SNPhood, a user-friendly *Bioconductor* R package to investigate and visualize the local neighborhood of a set of SNPs of interest for NGS data such as chromatin marks or transcription factor binding sites from ChIP-Seq or RNA- Seq experiments. SNPhood comprises a set of easy-to-use functions to extract, normalize and summarize reads for a genomic region, perform various data quality checks, normalize read counts using additional input files, and to cluster and visualize the regions according to the binding pattern. The regions around each SNP can be binned in a user-defined fashion to allow for analysis of very broad patterns as well as a detailed investigation of specific binding shapes. Furthermore, SNPhood supports the integration with genotype information to investigate and visualize genotype-specific binding patterns. Finally, SNPhood can be employed for determining, investigating, and visualizing allele-specific binding patterns around the SNPs of interest.

Author: Christian Arnold [aut, cre], Pooja Bhat [aut], Judith Zaugg [aut]

Maintainer: Christian Arnold <christian.arnold at embl.de>

Installation

To install this package, start R and enter:

## try http:// if https:// URLs are not supported
source("https://bioconductor.org/biocLite.R")
biocLite("SNPhood")

Documentation

To view documentation for the version of this package installed in your system, start R and enter:

browseVignettes("SNPhood")

 

HTML	R Script	Introduction and Methodological Details
HTML	R Script	Workflow example
PDF		Reference Manual
Text		NEWS

Details

biocViews	Software
Version	1.10.0
In Bioconductor since	BioC 3.2 (R-3.2) (3 years)
License	LGPL (>= 3)
Depends	R (>= 3.1), GenomicRanges, Rsamtools, data.table, checkmate
Imports	DESeq2, cluster, ggplot2, lattice, GenomeInfoDb, BiocParallel, VariantAnnotation, BiocGenerics, IRanges, methods, SummarizedExperiment, RColorBrewer, Biostrings, grDevices, gridExtra, stats, grid, utils, reshape2, scales, S4Vectors
LinkingTo
Suggests	BiocStyle, knitr, pryr, rmarkdown, SNPhoodData, corrplot
SystemRequirements
Enhances
URL	https://bioconductor.org/packages/SNPhood
BugReports	christian.arnold@embl.de
Depends On Me
Imports Me
Suggests Me
Links To Me
Build Report

Package Archives

Follow Installation instructions to use this package in your R session.

Source Package	SNPhood_1.10.0.tar.gz
Windows Binary	SNPhood_1.10.0.zip
Mac OS X 10.11 (El Capitan)	SNPhood_1.10.0.tgz
Source Repository	git clone https://git.bioconductor.org/packages/SNPhood
Source Repository (Developer Access)	git clone git@git.bioconductor.org:packages/SNPhood
Package Short Url	http://bioconductor.org/packages/SNPhood/
Package Downloads Report	Download Stats