RSVSim is a package for the simulation of deletions, insertions, inversion, tandem-duplications and translocations of various sizes in any genome available as FASTA-file or BSgenome data package. SV breakpoints can be placed uniformly accross the whole genome, with a bias towards repeat regions and regions of high homology (for hg19) or at user-supplied coordinates.
Package details |
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Author | Christoph Bartenhagen |
Bioconductor views | Sequencing |
Maintainer | Christoph Bartenhagen <c.bartenhagen@uni-koeln.de> |
License | LGPL-3 |
Version | 1.23.1 |
Package repository | View on GitHub |
Installation |
Install the latest version of this package by entering the following in R:
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