Copy Number Variation
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Updated
Jun 28, 2023
Copy Number Variation
Inference of subclonal populations in cancer genomes using smoothing splines
Container native virtualization disk build example
DupFinder: A tools to detect the duplicated genes using Illumina and Nanopore sequencing data
An adaptable method for analyzing SNVs, INDELs, and CNVs from Whole Exome Sequencing (WES) data, emphasizing germline variants.
Epicopy R package for CNV identification from methylation microarrays.
Workflow for running PennCNV with Affymetrix platform files
This project compares two learning paradigm, namely transfer-learning and self-supervised learning in a classification task of three retina disorders CNV, DME and DUSEN in addition to the normal condition using an OCT B-scans
A Snakemake pipeline for copy number variant calling without normal tissue samples
Python toolkit for parsing, processing, and analysis of Illumina methylation array IDAT files
A tool to call CNV (Copy Number Variation) from bulk ATAC-Seq data
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