EpicopyData companion data package for Epicopy.

eXome Hidden Markov model (XHMM) - Copy Number Variants (CNVs) from Whole Exome Sequencing Data

A fork of the project Excavator2 from sourceforge.

Copy number estimation of highly duplicated sequences

Epicopy R package for CNV identification from methylation microarrays.

A new CNV calling method for DNA-seq data

肿瘤体细胞突变检测流程（组织、cfDNA均可，需要有对照）

Light version of the bioinformatics tool "Patchwork"

A tool to call CNV (Copy Number Variation) from bulk ATAC-Seq data

Materials & Methods for CNV calling with Genalice software against a benchmark dataset

Short reads aligner for NIPT/CNV

A simple module for diagnostic variant information parsing

Workflow for running PennCNV with Illumina platform final report

Inference of subclonal populations in cancer genomes using smoothing splines

X11 related utilities for hts

Within-sample CNV calling

Using Convolutional Neural Networks to model an association between a genomic sequence and the number of sequenced reads that align to it

Workflow for running PennCNV with Affymetrix platform files

This is a group project