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Commit 608baf16 authored by nicolas.fernandez_ird.fr's avatar nicolas.fernandez_ird.fr :shinto_shrine:
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docs: add download procedure help picture

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# GeVarLi: GEnome assembly, VARiant calling and LIneage assignation #
# GeVarLi: GEnome assemblyA, VARiant calling and LIneage assignation #
![Author](<https://badgen.net/badge/Maintener/Nicolas Fernandez/blue?scale=0.9>)
![MacOSX Intel/M1/M2](<https://badgen.net/badge/icon/Hight Sierra (10.13.6) | Catalina (10.15.7) | Big Sure (11.6.3) | Monterey (12.6.0) | Ventura (13.3.1)/E6055C?icon=apple&label&list=|&scale=0.9>)
......@@ -159,7 +159,7 @@ conda update -n base -c defaults conda
### GeVarLi ###
**Clone** _to your home/_ [GeVarLi](https://forge.ird.fr/transvihmi/nfernandez/GeVarLi) GitLab IRDForge repository _(ID: 399)_ _(128Mo)_:
**Clone** _to your home/_ [GeVarLi](https://forge.ird.fr/transvihmi/nfernandez/GeVarLi) GitLab IRDForge repository _(ID: 399)_:
_(128 Mo required)_
```shell
......@@ -168,11 +168,17 @@ git clone --depth 1 https://forge.ird.fr/transvihmi/nfernandez/GeVarLi.git ~/GeV
**Update** GeVarLi:
```shell
cd ~/GeVarLi/ && git reset --hard HEAD && git pull --verbose
cd ~/GeVarLi/ && git reset --hard HEAD && git pull --depth 1 --verbose
```
Otherwise, you can**download** GeVarLi (no update through "git pull"):
Otherwise, you can just **download** GeVarLi (no update through "git pull"):
_(75 Mo required)_
![Image of download button](./resources/visuals/download_button.png)
<img src="./resources/visuals/download_button.png" width="400" height="100">
or
```shell
curl https://forge.ird.fr/transvihmi/nfernandez/GeVarLi/-/archive/main/GeVarLi-main.tar.gz -o ~/GeVarLi-main.tar.gz && \
tar -xzvf ~/GeVarLi-main.tar.gz && \
......@@ -185,7 +191,7 @@ rm -f ~/GeVarLi-main.tar.gz
1. Copy your **paired-end** reads files, in **.fastq.gz** format, into: **./resources/reads/** directory
_Without reads, SARS-CoV-2 from ./resources/test\_data/ directory will be used_
2. Execute **Start_GeVarLi.sh** bash script to run GeVarLi pipeline _(according to your choice)_:
2. Execute **Start_GeVarLi.sh** bash script to run GeVarLi pipeline:
- or with a **Double-click** on it _(if you make .sh files executable files with Terminal.app)_
- or with a **Right-click** > **Open with** > **Terminal.app**
- or with **CLI** from a terminal:
......@@ -198,7 +204,7 @@ _Option-1: Edit **config.yaml** file in **./configuration/** directory_
_Option-2: Edit **fastq-screen.conf** file in **./configuration/** directory_
First run will auto-created _(only once)_:
- Workflow-Base conda environment _(with: Snakemake, Mamba, Yq, Rename and GraphViz)_
- Workflow-Baseconda environment _(with: Snakemake, Mamba, Yq, Rename and GraphViz)_
- GeVarLi all tTools conda environments _(tools used by GeVarLi rules)_
- Indexes for BWA and BOWTIE2 aligners _(for each fasta genomes in resources/ directory)_
......@@ -285,9 +291,9 @@ _Some [temp] tagged files are removed by default, to save disk usage_
├── ⚙️ config.log
├── 📝 settings.log
├── 🍜 gevarli-base_v.{VERSION}.yaml
├── 🍜 gevarli-tools_v.{VERSION}.yaml
├── 📂 conda_env/
│ └── 📄 {TOOLS}_v.{version}.yaml
├── 📂 files-summaries
│ └── 📄 {PIPELINE}_files-summary.txt
├── 📂 graphs/
│ ├── 📈 {PIPELINE}_dag.{PNG/PDF}
│ ├── 📈 {PIPELINE}_filegraph.{PNG/PDF}
......@@ -565,8 +571,7 @@ _F1000Research (2021)_
**Documentation**: [https://snakemake.readthedocs.io/en/stable/index.html](https://snakemake.readthedocs.io/en/stable/index.html)
**Anaconda Software Distribution**
Team
_Computer software (2016)_
_Team-Computer software (2016)_
**DOI**: []()
**Publication**: [https://www.anaconda.com](https://www.anaconda.com)
**Source code**: [https://github.com/snakemake/snakemake](https://github.com/snakemake/snakemake) (conda)
......
resources/visuals/download_button.png

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