cnv-analysis
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Workflow for Sequenza, cellularity and ploidy
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Mar 14, 2025 - R
群体遗传学分析中用到的script和skill等
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Jul 6, 2024 - Python
CNV analysis based on the depth of coverage of Illumina data
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Sep 5, 2024 - Python
VizCNV is an interactive tool designed to analyze and visualize CNVs from short read WGS data in rare disease research. Built on R Studio Shiny, it streamlines the identification of complex genomic rearrangements and facilitates advancements in understanding and diagnosing rare genetic conditions.
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Apr 20, 2023 - R
An R package for detecting copy number variants from SNPs data
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Mar 4, 2025 - R
Pre-compiled absolute CNV data, which can be used for package sigminer/VSHunter and CNV analysis
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Jun 3, 2020
An R package to integrate and analyze CNV calling results from multiple methods in a uniformed and standardized manner
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Nov 16, 2021 - R
🧬🔍CNV analysis and outcome prediction in Ultra-High-Risk and First Episode Psychosis individuals 🩺🧠
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Aug 27, 2024 - Jupyter Notebook
Copy Number Variant Analyzer for Illumina Dragen files. Work in Progress...
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May 21, 2022 - Python
Powerful CNV calls filtering pipeline. Focused on fixed loci calling, before visual inspection.
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Dec 4, 2023 - R
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