Structural variant calling tutorial using long-reads.

Genome browser hub for the T2T genomes and resources

Multiple sequence alignment of long tandem repeats

Pan-genome inference and genotyping with long noisy or short accurate reads

Statistics and analysis for variation graphs

NVIDIA tools guide

Code from the "CUDA Crash Course" YouTube series by CoffeeBeforeArch

Renku provides a platform and tools for reproducible and collaborative data analysis.

HIP: C++ Heterogeneous-Compute Interface for Portability

Collaborative Collection of C++ Best Practices. This online resource is part of Jason Turner's collection of C++ Best Practices resources. See README.md for more information.

Magnificent app which corrects your previous console command.

Convert ASCII-armored PGP keys to animated QR code

A pairwise sequence aligner written in Rust

Pairwise nucleotide alignment benchmark of Rust bindings

List of Computer Science courses with video lectures.

Genome mapping and spliced alignment of cDNA or amino acid sequences

2022 WABI Pangenome workshop hackathon (AWS intro)

Cute tricks for SIMD vectorized binary encoding and decoding of nucleotides, in Rust.

Code to create a PRG from a Multiple Sequence Alignment file

GBWT in Rust

Simple succinct data structures (in Rust)

Detecting genome structural variants with deep learning in single molecule sequencing

A reimplementation of the WaveFront Alignment algorithm at low memory

📚 Modern C++ Tutorial: C++11/14/17/20 On the Fly | https://changkun.de/modern-cpp/

Toolset for SV simulation, comparison and filtering