A bioinformatics best-practice analysis pipeline for calling structural variants (SVs), copy number variants (CNVs) and repeat region expansions (RREs) from short DNA reads
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Updated
Sep 24, 2024 - Nextflow
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cnv
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DupFinder: A tools to detect the duplicated genes using Illumina and Nanopore sequencing data
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Updated
Sep 13, 2023 - Nextflow
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