[WIP] Evaluate outcomes from genome editing experiments
Repositories
nf-core repositories
Stochastic Testing and Input Manipulation for Unbiased Learning Systems
Compare the quality of multiple genomes, along with their annotations.
Precision HLA typing from next-generation sequencing data
k-mer similarity analysis pipeline
Generation of sequence-level annotations for amino acid sequences
Bioinformatics analysis pipeline for the functional annotation and translation of somatic SNVs/InDels and copy number abberations for precision cancer medicine using Personal Cancer Genome Reporter (PCGR). The pipeline offers germline SNVs/INDELS intepretation and annotation using Cancer Predisposition Sequencing Reporter (CPSR).