Full genome sequences for Homo sapiens (Human) as provided by UCSC (hg38, based on GRCh38.p12) with major allele injected from dbSNP151, and stored in Biostrings objects. Only single nucleotide variants (SNVs) were considered. At each SNV, the most frequent allele was chosen at the major allele to be injected into the reference genome.
Package details |
|
---|---|
Author | Jean-Philippe Fortin |
Bioconductor views | AnnotationData BSgenome Genetics Homo_sapiens |
Maintainer | Jean-Philippe Fortin <fortin946@gmail.com> |
License | CC BY-NC-ND 4.0 |
Version | 0.0.9999 |
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.