There are 1 repository under dna-sequencing topic.
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A method for variant graph genotyping based on exact alignment of k-mers
The first app for Mobile DNA Sequence Alignment and Analysis
Genotype Calling with Uncertainty from Sequencing Data in Polyploids 🍌🍓🥔🍠🥝
A collection of publications on comparison of high-throughput sequencing technologies.
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
Fast C code for identifying and removing primers and adapters
Generalizing deep learning-based variant callers via domain adaptation and semi-supervised learning
Classify DNA sequence into Binary class using different Classification algorithms.
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.
Data Structures And Algorithms
Projects related to Big Data course will be implemented in this repository.
Package to parse DNA kit files, and import them into Laravel
Implementation of BucketMap, a novel cache-efficient, bit-parallel and alignment-free short read mapping algorithm.
Identification of organisms from a stream of DNA sequences
Barcode Generator
A utility for splitting mixed origin NGS reads with secondary or alt mappings
MDI pipelines and apps for genome structural variant analysis by different library strategies
In this repository I backup the pipelines I write for the project I am involved
A python command line tool to turn a fastq and fasta to pickle files for ML or other analysis on python.
Jupyter notebooks for BFG-PCA related simulation and analysis.
Python based script which enables you to translate DNA or RNA, targeted towards high school biology. U=A G=C and exc.
DNA Sequence Converter made in Go
This is a script to align DNA sequences and do variant calling. (mtDNA working - poolseq under development)
Testing DNA sequences against various classification allgorithms
Get Started with DNA Sequencing working with .FastQ and .FastA file formats and performing Pattern Matching Algorithms (Exact & Approximate).
Shell workflow designed to process Whole Exome Sequencing (WES) data following GATK4 best practices for variant calling.