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TranspoScope

A Tool for Interactive Visualization of Evidence of Retrotransposon Insertions

Transposcope is a package that is used to evaluate potential retrotransposon insertions, which have been identified by either MELT or TIPseqHunter (A generic input type will be added in later releases).

As novel insertions are not present within the reference genome, reads are unable to be aligned correctly. TranspoScope solves this problem by creating a localized reference sequence that matches what was proposed by either MELT or TIPseqHunter. Reads which aligned to regions flanking the novel insertion are then realigned to the localized sequence.

TranspoScope includes functionality to visualize and assess the realigned regions within a web-based visualization.

Installation instructions

Install and Configure Anaconda / Miniconda

1. If Anaconda is not currently installed, install Miniconda using the installer and instructions available here, https://docs.conda.io/en/latest/miniconda.html#miniconda.
2. Set up the Bioconda channels as described in the following link, https://bioconda.github.io/#set-up-channels.

Create a Conda Environment and Install TranspoScope

Run the following command in the terminal:

conda create -n transposcope_env python=3.7 transposcope

This command will create a new conda environment called 'transposcope_env' which uses Python 3.7 and includes the transposcope package.

Alternatively, TranspoScope can be installed into the current conda environment using the following command.

conda install transposcope=2.0.1

Compatibility

TranspoScope has been tested on Linux and OSX. Realignment is not possible using regular conda on Windows as the Samtools conda package is not available on this platform. Viewing files which are hosted online will work on any operating system as long as a modern web browser is used.

https://github.com/FenyoLab/transposcope/wiki

Visualization Examples

TIPseq Examples

An example showing strong evidence of an insertion

This example shows strong evidence as there are ~800 bridging reads where one read aligns with the reference sequence, and the pair aligns with the LINE-1 reference.

interactive visualization link

An example showing less evidence of the insertion being real

This example is more difficult to classify as there are only one bridging reads and ten junction reads supporting the insertion.

interactive visualization link

Whole Genome Sequencing Examples

An example showing strong evidence of an insertion

This example shows strong evidence of there being an insertion. There are many bridging reads on both the 3' and 5' ends of the insertion as well as many junction reads, which match the proposed LINE-1 reference sequence.

interactive visualization link

An example showing almost no evidence of an insertion

This example shows little evidence that there is an insertion at this locus. Junction reads on the 5' flanking side match-three bases of the proposed LINE-1 reference sequence with no other matches.

interactive visualization link