eXome Hidden Markov model (XHMM) - Copy Number Variants (CNVs) from Whole Exome Sequencing Data
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Updated
Apr 26, 2017 - Shell
eXome Hidden Markov model (XHMM) - Copy Number Variants (CNVs) from Whole Exome Sequencing Data
Materials & Methods for CNV calling with Genalice software against a benchmark dataset
Workflow for running PennCNV with Illumina platform final report
Workflow for running PennCNV with Affymetrix platform files
Whole genome sequence simulation of DUF1220 domains and testing of alignment strategies
Walk through Red Hat MTV
A workflow for using SpeedSeq to align and call SVs from WGS data
Copy number variant caller and depth visualization utility for PacBio HiFi reads
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