Deployed medical apps on streamlit

Generalizing deep learning-based variant callers via domain adaptation and semi-supervised learning

Data Structures And Algorithms

A package primarily designed for analysing next generation sequencing DNA data from families with pedigree information in order to identify rare variants that are potentially causal of a disease/trait.

A utility for splitting mixed origin NGS reads with secondary or alt mappings

In this repository I backup the pipelines I write for the project I am involved

Jupyter notebooks for BFG-PCA related simulation and analysis.

A python command line tool to turn a fastq and fasta to pickle files for ML or other analysis on python.

Python based script which enables you to translate DNA or RNA, targeted towards high school biology. U=A G=C and exc.

A simple bioinformatics application for DNA sequence analysis using machine learning techniques, implemented in Python.

First Draft OF MediCrypt . Checkout GitHub Repo: MediCrypt Instead!

DNA Pattern Finder is a tool that highlights known or custom patterns in a user-provided DNA sequence using a Tkinter interface for color-coded matches. Perfect for quick analysis or educational exploration.

CloudBioLinux: configure virtual (or real) machines with tools for biological analyses

DNA - CS50

This is a Hospital Communication System Using DNA Encryption and Image Steganography This project enables secure communication between two hospitals, Hospital A and Hospital B, by encrypting and hiding sensitive patient data within images using DNA encryption and Least Significant Bit (LSB) steganography techniques, powered by Socket.IO

A long read nanopore genome assembly and error correction pipeline

DNAxplorer by BisdakBioTech is our final project submission for LBYBE1B. Submitted by Raphael C. Murillo and Niru Miguel Dagoy

Implementation of LAVA algorithm in Seq language.

Nextflow pipeline for disease QTL mapping and follow up analyses

Jupyter notebooks for BFG-PCA related simulation and analysis.