Stars
Unix, R and python tools for genomics and data science
GUI/CommandLine Tool Box for biologistists to utilize NGS data.
A One-Click System for Analyzing Loop-Resolution Hi-C Experiments
MUM&Co uses Whole Genome Alignment information provided by MUMmer (only v4) to detect Structural Variation
Pipeline for structural variant image curation and analysis.
Methods to integrate data from multiple genome sequencing datasets and form consensus variant calls
An easy way to run BioNano genomic analysis
Accurate Typing of Human Leukocyte Antigen (HLA) by Oxford Nanopore Sequencing
https://www.sib.swiss/training/course/2017-11-longreads
Structural variant benchmark using PacBio HiFi reads