Revolutionizing DNA analysis and making it accessible to all through innovative AI-powered analysis and interpretive tools

A method for variant graph genotyping based on exact alignment of k-mers

The first app for Mobile DNA Sequence Alignment and Analysis

A collection of publications on comparison of high-throughput sequencing technologies.

Genotype Calling with Uncertainty from Sequencing Data in Polyploids 🍌🍓🥔🍠🥝

Sentieon DNAseq

Fake genomes, fake sequencing, real insights.

Deployed medical apps on streamlit

The repository contains the source code of the NanoForms server (Czmil et al. NanoForms: an integrated server for processing, analysis and assembly of raw sequencing data of microbial genomes, from Oxford Nanopore technology. PeerJ, 2022). It is meant to be the source for standalone server installation. https://doi.org/10.7717/peerj.13056

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

Fast C code for identifying and removing primers and adapters

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.

Data Structures And Algorithms

Classify DNA sequence into Binary class using different Classification algorithms.

Tool for generating artificial fastq files which can be used for testing the fidelity of NGS analysis pipelines.

Tools for encoding files to DNA sequence

Package to parse DNA kit files, and import them into Laravel

Projects related to Big Data course will be implemented in this repository.

Implementation of BucketMap, a novel cache-efficient, bit-parallel and alignment-free short read mapping algorithm.

R-package to analyse and quantify aberrations in DNA-sequencing data