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ClairS - a deep-learning method for long-read somatic small variant calling

Genomeanalysismodule ⭐ 21

Welcome to the website and github repository for the Genome Analysis Module. This website will guide the learning experience for trainees in the UBC MSc Genetic Counselling Training Program, as they embark on a journey to learn about analyzing genomes.

Fraggenescanrs ⭐ 10

Better and faster Rust implementation of the FragGeneScan gene prediction model for short and error-prone reads.

A scalable variant calling and benchmarking framework supporting both short and long reads.

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