SVIndelGenotyper was employed for analyzing the error profiles of indels and structural variants in deep sequencing data.
Explore the docs »
Read the paper »
Request Feature
|
Report Bug
⭐ Consider starring the repo! ⭐
SVIndelGenotyper depends on python >= 3.9.9
> git clone https://github.com/stjude/SVIndelGenotyper.git
> cd SVIndelGenotyper
> ./make_install.sh
SVIndelGenotyper has 2 subcommands:
indel
genotype indels for sequencing data (WGS/WES/RNASeq)sv
genotype SVs for sequencing data (WGS)
> python SVIndelGenotyper.py indel testIndel.tsv
> python SVIndelGenotyper.py sv testSV.tsv
Manuscript under preparation
- Yanling.Liu[AT]stjude.org
- Pandurang.Kolekar[AT]stjude.org
- Xiaotu.Ma[AT]stjude.org
Copyright 2023 St. Jude Children's Research Hospital
Licensed under the Apache License, Version 2.0 (the "License"); you may not use this file except in compliance with the License. You may obtain a copy of the License at
http://www.apache.org/licenses/LICENSE-2.0
Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an "AS IS" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License.