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This repository is tailored for experienced Python users and contains a personal collection of Python scripts for bioinformatics. Focused on sequencing analysis, data processing, and data visualization, these scripts utilize powerful libraries such as NumPy, pandas, and seaborn.

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BioInfoPythonScripts

Welcome to BioInfoPythonScripts! This repository is tailored for experienced Python users and contains a personal collection of Python scripts for bioinformatics. Focused on sequencing analysis, data processing, and data visualization, these scripts utilize powerful libraries such as NumPy, pandas, and seaborn. Whether you're working on genome sequencing, RNA-seq data analysis, or complex data visualizations, you'll find useful tools and examples here to enhance your bioinformatics workflows. Dive into efficient, well-documented code designed to tackle real-world bioinformatics challenges.

Introduction

This repository provides a collection of Python scripts designed for bioinformatics tasks. The scripts are intended for users who have a solid understanding of Python and are looking to apply their skills to bioinformatics challenges.

Prerequisites

Before using these scripts, ensure you have the following installed:

  • Python 3.6 or higher
  • NumPy
  • pandas
  • seaborn
  • Biopython
  • Matplotlib

You can install these dependencies using pip:

pip install numpy pandas seaborn biopython matplotlib scikit-learn

Repository Structure

BioInfoPythonScripts/
├── README.md
├── requirements.txt
├── CONTRIBUTING.md
├── LICENSE
├── data_processing/
│   ├── README.md
│   ├── parsing_and_extraction/
│   ├── data_transformation/
│   ├── data_merging/
│   └── ...
├── visualization/
│   ├── README.md
│   ├── scatter_and_bubble_plots/
│   ├── violin_and_box_plots/
│   ├── bar_and_stacked_plots/
│   ├── venn_diagrams/
│   └── ...
├── quality_control/
│   ├── README.md
│   ├── coverage_analysis/
│   ├── fastqc_parsing/
│   ├── metrics_extraction/
│   └── ...
├── report_generation/
│   ├── README.md
│   ├── wgs_reports/
│   ├── rna_reports/
│   ├── somalier_reports/
│   └── ...
├── workflow_utilities/
│   ├── README.md
│   ├── sample_sheet_generation/
│   ├── workflow_generation/
│   ├── workflow_monitoring/
│   └── ...
├── genetics_analysis/
│   ├── README.md
│   ├── somalier_analysis/
│   ├── variant_calling/
│   ├── snp_analysis/
│   └── ...
└── utilities/
    ├── __init__.py
    ├── file_parsers.py
    └── plotting_utils.py

Contributing

Contributions are what makes the open-source community such an amazing place to learn, inspire, and create. Any contributions you make are greatly appreciated.

If you have a suggestion that would make this better, please fork the repo and create a pull request. You can also simply open an issue with the tag "enhancement". Don't forget to give the project a star! Thanks again!

About

This repository is tailored for experienced Python users and contains a personal collection of Python scripts for bioinformatics. Focused on sequencing analysis, data processing, and data visualization, these scripts utilize powerful libraries such as NumPy, pandas, and seaborn.

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