New version with the changes (PR #4)

New version with the changes

.github/workflows/actions.yml

@@ -5,7 +5,7 @@ jobs:
     runs-on: ubuntu-latest
     strategy:
       matrix:
-        python-version: [3.5, 3.6, 3.7, 3.8]
+        python-version: [3.6, 3.7, 3.8]
     steps:
     - uses: actions/checkout@v2
     - name: Set up Python ${{ matrix.python-version }}
@@ -19,4 +19,4 @@ jobs:
     - name: Test a single transcript
       run: |
         # Test the script by retrieving a transcript data
-        python gnomad_python_api.py -filter_by="gene_name" -search_by="TP53" -dataset="gnomad_r2_1"
+        python gnomad_api_cli.py -filter_by=gene_name -search_by="BRCA1" -dataset="gnomad_r2_1" -sv_dataset="gnomad_sv_r2_1"

.gitignore

@@ -0,0 +1,3 @@
+.ipynb_checkpoints
+outputs/
+outputs/*

README.md

@@ -1,61 +1,145 @@
-# 🧬 gnomAD Python API (Batch Script)
+# 🧬 gnomAD Python API
 
 ![Actions for gnomad_python_api](https://github.com/furkanmtorun/gnomad_python_api/workflows/Actions%20for%20gnomad_python_api/badge.svg)
+![Python Badges](https://img.shields.io/badge/Tested_with_Python-3.6%20%7C%203.7%20%7C%203.8-blue)
+![gnomAD Python API License](https://img.shields.io/badge/License-%20GPL--3.0-green)
+
+- [🧬 gnomAD Python API](#-gnomad-python-api)
+  - [:hash: What is *gnomAD* and the purpose of this script?](#hash-what-is-gnomad-and-the-purpose-of-this-script)
+  - [:hash: Requirements and Installation](#hash-requirements-and-installation)
+  - [:hash: GUI | Usage](#hash-gui--usage)
+  - [:hash: CLI | Usage & Options](#hash-cli--usage--options)
+  - [:hash: CLI | Example Usages](#hash-cli--example-usages)
+  - [:hash: Disclaimer](#hash-disclaimer)
+  - [:hash: Contributing & Feedback](#hash-contributing--feedback)
+  - [:hash: Citation](#hash-citation)
+  - [:hash: Developer](#hash-developer)
+  - [:hash: References](#hash-references)
 
 ## :hash: What is *gnomAD* and the purpose of this script?
-[gnomAD (The Genome Aggregation Database)](http://gnomad.broadinstitute.org/) is aggregation of thousands of exomes and genomes human sequencing studies. Also, gnomAD consortium annotates the variants with allelic frequency in genomes and exomes.
-**Here**, this batch script is able to search the genes or transcripts of your interest and retrieve variant data from the database via [gnomAD backend API](https://gnomad.broadinstitute.org/api) that based on GraphQL query language.
+[gnomAD (The Genome Aggregation Database)](http://gnomad.broadinstitute.org/) [[1]](#hash-references) is aggregation of thousands of exomes and genomes human sequencing studies. Also, gnomAD consortium annotates the variants with allelic frequency in genomes and exomes.
+
+**Here**, this API with both CLI and GUI versions is able to search the genes or transcripts of your interest and retrieve variant data from the database via [gnomAD backend API](https://gnomad.broadinstitute.org/api) that based on GraphQL query language.
 
 ## :hash: Requirements and Installation
- - Create a directory and download the "**gnomad_python_api.py**" and "**requirements.txt**" files or clone the repository via Git using following command:
+ - Create a directory and download the "**gnomad_api_cli.py**" and "**requirements.txt**" files or clone the repository via Git using following command:
 
  	`git clone https://github.com/furkanmtorun/gnomad_python_api.git`
 
  - Install the required packages if you do not already:
 
-	` pip3 install -r requirements.txt `
+	` pip3 install -r requirements.txt`
+
+  > The `requirements.txt` contains required libraries for both GUI (graphical user interface) and CLI (command-line interface) versions.
 
 - It's ready to use now! 
 
 > If you did not install **pip** yet, please follow the instruction [here](https://pip.pypa.io/en/stable/installing/).
 
-## :hash: Usage & Options
-| Options in the script | Description | Parameters |
+## :hash: GUI | Usage
+
+In the GUI version of gnomAD Python API, [Streamlit](https://www.streamlit.io/) has been used.
+
+> **Note:** In GUI version, it is possible to generate plots from the data retrieved. 
+> This option is not available in CLI version since it is still under development. 
+>
+> **So, it is recommended to use GUI version.**
+
+- To use GUI version of gnomAD Python API:
+
+  `streamlit run gnomad_api_gui.py`
+
+
+- Here are the screenshots for the GUI version:
+
+  ![gnomAD Python API GUI](img/main_screen.png)
+
+  _gnomAD Python API GUI - Main Screen_
+
+  ![gnomAD Python API GUI](img/results.png)
+
+  _gnomAD Python API GUI - Outputs_
+
+  ![gnomAD Python API GUI](img/results_2.png)
+
+  _gnomAD Python API GUI - Outputs and Plots_
+
+> The outputs are also saved into `outputs/` folder in the GUI version. 
+
+## :hash: CLI | Usage & Options
+| Options | Description | Parameters |
 |--|--|--|
-| -filter_by | *It defines the input type* |gene_name, gene_id, transcript_id |
-| -search_by | *It defines the input* | Type a gene/transcript identifier <br> *e.g.: TP53, ENSG00000169174, ENST00000544455* <br> Type the name of file containig your inputs <br> *e.g: myGenes.txt*
-| -dataset | *It defines the dataset* | exac, gnomad_r2_1, gnomad_r3, gnomad_r2_1_controls, gnomad_r2_1_non_neuro, gnomad_r2_1_non_cancer, gnomad_r2_1_non_topmed
-| -h | It displays the parameters | *To get help via script:* `python gnomad_python_api.py -h`
+| -filter_by | *It defines the input type.* |`gene_name`, `gene_id`, `transcript_id`, or  `rs_id` |
+| -search_by | *It defines the input.* | Type a gene/transcript identifier <br> *e.g.: TP53, ENSG00000169174, ENST00000544455* <br> Type the name of file containig your inputs <br> *e.g: myGenes.txt*
+| -dataset | *It defines the dataset.* | `exac`, `gnomad_r2_1`, `gnomad_r3`, `gnomad_r2_1_controls`, `gnomad_r2_1_non_neuro`, `gnomad_r2_1_non_cancer`, or `gnomad_r2_1_non_topmed`
+| -sv_dataset | *It defines structural variants dataset.* | `gnomad_sv_r2_1`, `gnomad_sv_r2_1_controls`, or `gnomad_sv_r2_1_non_neuro`
+| -reference_genome | *It defines reference genome build.* | `GRCh37` or `GRCh38`
+| -h | *It displays the parameters.* | *To get help via script:* `python gnomad_api_cli.py -h`
+
 
-## :hash: Example Usages
+> ❗ Here, for getting variants, `gnomad_r2_1` and `gnomad_sv_r2_1` are defined as default values for these two `-dataset` and `-sv_dataset` options, respectively.
+>
+>
+> ❗ Also, you need to choose `GRCh38` for retrieving variants from the `gnomad_r3` dataset. However, in the `GRCh38` build, structural variants are not available. 
+
+## :hash: CLI | Example Usages
 - **How to list the variants by gene name or gene id?**
 
-`python gnomad_python_api.py -filter_by="gene_name" -search_by="TP53" -dataset="gnomad_r2_1"`
+  *For gene name:*
+
+  `python gnomad_api_cli.py -filter_by=gene_name -search_by="BRCA1" -dataset="gnomad_r2_1" -sv_dataset="gnomad_sv_r2_1"`
 
-> Here,  "**gene_id**" can also be used instead of "**gene_name**" after stating an **Ensembl Gene ID** instead of a gene name.
+  If you get data from `gnomad_r3`:
+
+  `python gnomad_api_cli.py -filter_by=gene_name -search_by="BRCA1" -dataset="gnomad_r3" -reference_genome="GRCh38"`
+
+  *For Ensembl gene ID* 
+
+  `python gnomad_api_cli.py -filter_by=gene_id -search_by="ENSG00000169174" -dataset="gnomad_r2_1" -sv_dataset="gnomad_sv_r2_1"`
 
 - **How to list the variants by transcript ID?**
 
-`python gnomad_python_api.py -filter_by="transcript_id" -search_by="ENST00000544455" -dataset="gnomad_r3"`
+  `python gnomad_api_cli.py -filter_by=transcript_id -search_by="ENST00000407236" -dataset="gnomad_r2_1"`
+
+- **How to get variant info by RS ID (rsId)?**
+
+  `python gnomad_api_cli.py -filter_by=rs_id -search_by="rs201857604" -dataset="gnomad_r2_1"`
 
 - **How to list the variants using a file containing genes/transcripts?**
 
-  - Prepare your file that contains gene name, Ensembl gene IDs or Ensembl transcript IDs line-by-line. 
+  - Prepare your file that contains gene name, Ensembl gene IDs, Ensembl transcript IDs or RS IDs line-by-line. 
 	> ENSG00000169174 <br> ENSG00000171862  <br> ENSG00000170445
 
   - Then, run the following command:
 
-  `python gnomad_python_api.py -filter_by="gene_id" -search_by="myFavoriteGenes.txt" -dataset="exac"`
+    `python gnomad_api_cli.py -filter_by="gene_id" -search_by="myFavoriteGenes.txt" -dataset="gnomad_r2_1" -sv_dataset="gnomad_sv_r2_1"`
 
-> Please, use only one type of identifier in the file.
+  > Please, use only one type of identifier in the file.
 
-- Then, the variants will be listed in "**outputs**" folder in the files according to their identifier (gene name, gene id or transcript id).  
+- Then, the variants will be listed in "**outputs**" folder in the folders according to their identifier (gene name, gene id, transcript id or rsId).
+
 -  That's all!
 
+## :hash: Disclaimer
+All the outputs provided by this tool are for informational purposes only. 
+
+The information is not intended to replace any consultation, diagnosis, and/or medical treatment offered by physicians or healthcare providers.
+
+The author of the app will not be liable for any direct, indirect, consequential, special, exemplary, or other damages arising therefrom.
+
 ## :hash: Contributing & Feedback
-I would be very happy to see any feedbacks and contributions on the script.
+I would be very happy to see any feedback or contributions to the project.
+
+For problems and enhancement requests, please `open an issue` above. 
+
+## :hash: Citation
+Upcoming !
 
-**Furkan Torun |  [[email protected]](mailto:[email protected]) | Website: [furkanmtorun.github.io](https://furkanmtorun.github.io/)**
+## :hash: Developer
+**Furkan M. Torun ([@furkanmtorun](http://github.com/furkanmtorun)) |  [[email protected]](mailto:[email protected]) |
+Academia: [Google Scholar Profile](https://scholar.google.com/citations?user=d5ZyOZ4AAAAJ)**
 
+## :hash: References
+1. Karczewski, K.J., Francioli, L.C., Tiao, G. et al. The mutational constraint spectrum quantified from variation in 141,456 humans. Nature 581, 434–443 (2020). https://doi.org/10.1038/s41586-020-2308-7