Copy Number Variants

Identification of Copy Number Variants from SNP Arrays using PennCNV.- Using SAAS-CNV to Detect and Characterize Somatic Copy Number Alterations in Cancer Genomes from Next Generation Sequencing and SNP Array Data.- Statistical Detection of Genome Differences Based on CNV Segment.- Whole Genome Shotgun Sequence CNV Detection using Read Depth.- Read Depth Analysis to Identify CNV in Bacteria using CNOGpro.- Using HaMMLET for Bayesian Segmentation of WGS read-depth Data.- Split-Read InDel and Structural Variant Calling Using PINDEL.- Detecting Small Inversions using SRinversion.- Detection of CNVs in NGS data using VS-CNV.- Structural Variant Breakpoint Detection with novoBreak.- Use of RAPTR-SV to Identify SVs from Read Pairing and Split Read Signatures.- Versatile Identification of Copy Number Variants with Canvas.- Analysis of Population-genetic Properties of Copy Number Variations.- Validation of Genomic Structural Variants through Long Sequencing Technologies.- Structural Variation Detection and Analysis using Bionano Optical Mapping.