iAnnotateSV is a Python library and command-line software toolkit to annotate and visualize structural variants detected from Next Generation DNA sequencing data.
Project description
iAnnotateSV: Annotation of structural variants detected from NGS
Author: Ronak H Shah
Contributors : Gowtham Jayakumaran and Ian Johonson
Contact: rons.shah@gmail.com
Source code: http://github.com/rhshah/iAnnotateSV
License: Apache License 2.0
iAnnotateSV is a Python library and command-line software toolkit to annotate and visualize structural variants detected from Next Generation DNA sequencing data. This works for majority is just re-writing of a tool called dRanger_annotate written in matlab by Mike Lawrence at Broad Institue. But it also has some additional functionality and control over the annotation w.r.t the what transcripts to be used for annotation. It is designed for use with hybrid capture, including both whole-exome and custom target panels, and short-read sequencing platforms such as Illumina.
Citation
We are in the process of publishing a manuscript describing iAnnotateSV as part of the Structural Variant Detection framework. If you use this software in a publication, for now, please cite our website iAnnotateSV.
Acknowledgements
I would like to thanks Mike Lawrence from Broad Institute for sharing his code and Michael Berger for his insights into the dRanger_annotate tool.
Required Packages
We require that you install:
python: v3.10
pandas: v2.2.2
biopython: v1.84
Pillow: v10.4.0
openpyxl: v3.1.5
reportlab: v3.6.13
coloredlogs: v15.0.1
Utilities
Generate Fusion Peptides - Helen Xie
Quick Usage
If you know python I have created a small test script in /iAnnotateSV/test directory it runs a test on existing code and compares the result with the output file.
Else To Run:
-
If you want to run with default options:
python /path/to/iAnnotateSV.py -i svFile.txt -ofp outputfilePrefix -o /path/to/output/dir -r hg19 -d 3000
-
If you want to run with your own transcripts:
python path/to/path/to/iAnnotateSV.py -i svFile.txt -ofp outputfilePrefix -o /path/to/output/dir -r hg19 -d 3000 -c canonicalTranscripts.txt
-
If you want to run with your own transcripts & make plots (making plots is a test module only):
python path/to/iAnnotateSV.py -i svFile.txt -ofp outputfilePrefix -o /path/to/output/dir -r hg19 -d 3000 -c canonicalTranscripts.txt -u uniprot.txt -p
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