Our method integrates information from all sequenced samples, thus avoiding loss of alleles due to low coverage. Moreover, it increases the statistical power to uncover sequencing or alignment errors <doi:10.1093/plphys/kiad191>.
Package details |
|
---|---|
Bioconductor views | GenomeAnnotation HiddenMarkovModel Sequencing |
Maintainer | |
License | GPL (>= 2) |
Version | 2.1.0 |
Package repository | View on GitHub |
Installation |
Install the latest version of this package by entering the following in R:
|
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.