Tool for low-coverage whole-genome imputation
"GLIMPSE2 is a set of tools for low-coverage whole genome sequencing imputation. GLIMPSE2 is based on the GLIMPSE model and designed for reference panels containing hundreads of thousands of reference samples, with a special focus on rare variants."
- The description above refers to the software: https://odelaneau.github.io/GLIMPSE/
- I have packaged the software as a snap for personal use but I have made the snap available for free.
- I do not maintain the software itself. I only maintain the snap packaging. Please report software bugs to the maintainers.
- Report snap-specific bugs to me.
- I DO use this snap. It HAS PASSED ALL THE PROVIDED TESTS on my system. I do not track the latest version.
- Packaging 'style' : binary for linux machines.
- License refers to the original software, not the snapcraft 'code'.
- Run the following to rename the snap commands to GLIMPSE2_<command>
```sudo snap alias rjd-glimpse.chunk GLIMPSE2_chunk```
```sudo snap alias rjd-glimpse.concordance GLIMPSE2_concordance```
```sudo snap alias rjd-glimpse.ligate GLIMPSE2_ligate```
```sudo snap alias rjd-glimpse.phase GLIMPSE2_phase```
```sudo snap alias rjd-glimpse.split-reference GLIMPSE2_split_reference```