breakpoints: Putative breakpoints of chimeric reads

In R453Plus1Toolbox: A package for importing and analyzing data from Roche's Genome Sequencer System

Description

This example holds two consensus (pathogenic and reciproce) breakpoints of 12 chimeric reads indicating an inversion on chromosome 16. The Breakpoints object gives access to the breakpoint locations as well as alignment information for each of the 12 reads.

Usage

data(breakpoints)

Format

Formal class 'Breakpoints'

Source

‘Targeted next-generation sequencing detects point mutations, insertions, deletions, and balanced chromosomal rearrangements as well as identifies novel leukemia-specific fusion genes in a single procedure’ (Leukemia, submitted)

Examples

    data(breakpoints)

R453Plus1Toolbox documentation built on Nov. 8, 2020, 5:59 p.m.