Snakemake-based workflow for detecting structural variants in genomic data
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Updated
Feb 13, 2024 - Python
Snakemake-based workflow for detecting structural variants in genomic data
Population-wide Deletion Calling
A combination of optical genome mapping with Bionano and whole genome sequencing short-read data. This pipeline was created to help integrate structural variant calling from these two technologies.
Comparing performance of SV callers when using NovoAlign compared to other aligners.
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