This package provides a set of functions for NGS data processing, quality analysis, filtering and demultiplexing. These functions are designed to be applied in consecutive order on Miseq raw data to obtain a set of intersected haplotypes for each evaluated sample. With these consensus haplotypes different kinds of computations can be made, i.e genotyping, variant calling and quasispecies diversity.
Package details |
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Author | Alicia Aranda Fernandez |
Maintainer | Alicia Aranda <ali.afernandez99@gmail.com> |
License | CC BY 4.0 |
Version | 0.1.0 |
Package repository | View on GitHub |
Installation |
Install the latest version of this package by entering the following in R:
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