jackalope: A Swift, Versatile Phylogenomic and High-Throughput Sequencing Simulator

Simply and efficiently simulates (i) variants from reference genomes and (ii) reads from both Illumina <https://www.illumina.com/> and Pacific Biosciences (PacBio) <https://www.pacb.com/> platforms. It can either read reference genomes from FASTA files or simulate new ones. Genomic variants can be simulated using summary statistics, phylogenies, Variant Call Format (VCF) files, and coalescent simulations—the latter of which can include selection, recombination, and demographic fluctuations. 'jackalope' can simulate single, paired-end, or mate-pair Illumina reads, as well as PacBio reads. These simulations include sequencing errors, mapping qualities, multiplexing, and optical/polymerase chain reaction (PCR) duplicates. Simulating Illumina sequencing is based on ART by Huang et al. (2012) <doi:10.1093/bioinformatics/btr708>. PacBio sequencing simulation is based on SimLoRD by Stöcker et al. (2016) <doi:10.1093/bioinformatics/btw286>. All outputs can be written to standard file formats.

Package details

AuthorLucas A. Nell [cph, aut, cre] (<https://orcid.org/0000-0003-3209-0517>)
MaintainerLucas A. Nell <[email protected]>
LicenseMIT + file LICENSE
Version0.1.3
URL https://github.com/lucasnell/jackalope
Package repositoryView on CRAN
Installation Install the latest version of this package by entering the following in R:
install.packages("jackalope")

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jackalope documentation built on Oct. 30, 2019, 11:47 a.m.