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whole-genome-sequencing x

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Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing

Pipeline Structural Variation ⭐ 87

Pipeline for calling structural variations in whole genomes sequencing Oxford Nanopore data

JARVIS: a comprehensive deep learning framework to prioritise non-coding variants in whole genomes

Nextflow bioinformatics pipeline for large-scale analysis of Multiple Myeloma genomes

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