junctionCompatible

junctions

<code>IRangesList</code> of exonic regions, one entry
per fragment

frag_exonic

<code>IRangesList</code> of introns, one entry per fragment

frag_intron

min_anchor

Logical indicating whether counts or indices of
compatible fragments should be returned

counts


Identify fragments compatible with splice junctions.


internal

SGSeq is a software package for analyzing splice events from
RNA-seq data. Input data are sequence reads mapped to a reference
genome in BAM format. Genes are represented as a genome-wide
splice graph, which can be obtained from existing annotation or
can be predicted from the data. Splice events are identified
from the graph and are quantified locally using structurally
compatible reads at the start or end of each splice variant.
The package includes functions for splice event prediction,
quantification, visualization and interpretation.

junctionCompatible: Compatible fragment counts for splice junctions

Description

Usage

Arguments

Value