#计算机科学#Precision genomics for everyone, everywhere. Powered by private AI.
A method for variant graph genotyping based on exact alignment of k-mers
#IOS#The first app for Mobile DNA Sequence Alignment and Analysis
Genotype Calling with Uncertainty from Sequencing Data in Polyploids 🍌🍓🥔🍠🥝
#Awesome#A collection of publications on comparison of high-throughput sequencing technologies.
Fake genomes, fake sequencing, real insights.
#计算机科学#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 Ox...
Fast C code for identifying and removing primers and adapters
#计算机科学#Classify DNA sequence into Binary class using different Classification algorithms.
#计算机科学#Generalizing deep learning-based variant callers via domain adaptation and semi-supervised learning
Scripts for bioinformatics analysis of sequencing data
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...
Tool for generating artificial fastq files which can be used for testing the fidelity of NGS analysis pipelines.
#计算机科学#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.
Package to parse DNA kit files, and import them into Laravel