GitHub - tgac-vumc/ACE: Absolute Copy Number Estimation using low-coverage whole genome sequencing data

Absolute Copy Number Estimation using low-coverage whole genome sequencing data - tgac-vumc/ACE

Copy number analysis by low coverage whole genome sequencing using ultra low-input DNA from formalin-fixed paraffin embedded tumor tissue, Genome Medicine

Assessing Copy Number Alterations in Targeted, Amplicon-Based Next-Generation Sequencing Data - ScienceDirect

American Society for Clinical Pharmacology and Therapeutics - 2019 - Clinical Pharmacology & Therapeutics - Wiley Online Library

American Society for Clinical Pharmacology and Therapeutics - 2019 - Clinical Pharmacology & Therapeutics - Wiley Online Library

Comprehensive Assessment of Somatic Copy Number Variation Calling Using Next-Generation Sequencing Data

GitHub - mbourgey/EBI_cancer_workshop_CNV: hands-on for NGS/SNParray CNV call trainning

PDF) HBOS-CNV: A New Approach to Detect Copy Number Variations From Next-Generation Sequencing Data

PDF) OTSUCNV: an adaptive segmentation and OTSU-based anomaly classification method for CNV detection using NGS data

PDF) HBOS-CNV: A New Approach to Detect Copy Number Variations From Next-Generation Sequencing Data