trueSNVs {deepSNV} | R Documentation

## Example .bam data and true SNVs.

### Description

Two .bam alignments as example data sets are downloaded remotely via http. Sequenced were a 1,512 nt fragment of the HIV genome and a mixture (90% + 10%) with another variants. The two sequences were confirmed by Sanger sequencing and stored in the table trueSNVs.

### Examples

    data(HIVmix)
    data(trueSNVs)
    table(p.adjust(p.val(HIVmix), method="BH") < 0.05, trueSNVs)

[Package deepSNV version 1.38.0 Index]