There are 3 repositories under genotyping topic.
C++ library and cmdline tools for parsing and manipulating VCF files with python and zig bindings
:floppy_disk: :page_with_curl: "Reads to report" for public health and clinical microbiology
Efficient genotyping bi-allelic SNPs on single cells
A method for variant graph genotyping based on exact alignment of k-mers
Pileup biallelic SNPs from single-cell and bulk RNA-seq data
A method for circular DNA detection based on probabilistic mapping of ultrashort reads
Toolkit for VNTR genotyping and repeat-pan genome graph construction
Towards fast and accurate SNP genotyping from whole genome sequencing data for bedside diagnostics.
Polyploid micro-haplotype assembly using Markov chain Monte Carlo simulation.
Bayesian non-parametric clustering (BnpC) of binary data with missing values and uneven error rates
An efficient genetic data imputation pipeline
A simple python library to identify the most likely strain from the population
Visualisation application for Klebsiella genotypes generated by Kleborate.
Screening Historical Events of Recombination in a Phylogeny via Ancestral Sequences
SV genotyper for long reads with a variation graph
Python package for microsatellite genotyping from highly multiplexed amplicon sequencing data
Repository of SmoothDescent R package. Smooth Descent is a map-cleaning algorithm that can calculate identity by descent probabilities and correct genotyping errors based on marker maps.
A nextflow pipeline for calling and annotating small germline variants from short DNA reads for WES and WGS data
This repository is my collection of pipelines for basic GWAS analysis, written in R to simplify, please cite original tools/approaches referred in the pipelines.
HBVouroboros automates sequencing-based HBV genotyping and expression profiling
Genotyping MUltiplexed-Sequencing of CRISPR-Localized Editing
GBS workflow using dDocent. This was designed to process GBS data from SEACONNECT project.
A macOS application for microsatellite genotyping using capillary sequencing data.
Establishing genotype-phenotype links using Bulk Segregant Analysis of mutations in Plant populations