nWGS_pipeline_refdata

nWGS_pipeline is a comprehensive bioinformatics workflow designed for the analysis of Central Nervous System (CNS) tumor samples using Oxford Nanopore sequencing data. It integrates multiple analytical modules, including copy number variation (CNV) detection, DNA methylation profiling, structural variant calling, and MGMT promoter methylation status assessment. Users can access the reference materials, example datasets, and detailed usage instructions via the project's GitHub repository.For references and licensing terms, see:🔗 https://github.com/VilhelmMagnusLab/nWGS_pipeline