A structural variation pipeline for short-read sequencing
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Updated
May 21, 2024 - Python
A structural variation pipeline for short-read sequencing
Snakemake-based workflow for detecting structural variants in genomic data
🔍 Post Assembly Variants Finder
Clinical Whole Genome and Exome Sequencing Pipeline
PhenoSV: Interpretable phenotype-aware model for the prioritization of genes affected by structural variants.
Snakemake-based workflow for generating artificial genomes with structural variants
A snakemake workflow for regions of difference discovery in Mycobacterium tuberculosis complex (MTBC) samples
Genome assembly and variant benchmarks for Chinese Quartet
Long read structural variants in rare disease cohort
In this repository I backup the pipelines I write for the project I am involved
The experiments performed in State-of-the-art structural variant calling: What went conceptually wrong and how to fix it?
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