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

Evaluation of tools for identifying large copy number variations from ultra- low-coverage whole-genome sequencing data, BMC Genomics

GATK-gCNV enables the discovery of rare copy number variants from exome sequencing data

Shallow whole-genome sequencing of plasma cell-free DNA accurately differentiates small from non-small cell lung carcinoma, Genome Medicine

DNA copy number profiling: from bulk tissue to single cells

CODEX2: full-spectrum copy number variation detection by high-throughput DNA sequencing, Genome Biology

Low-pass whole-genome sequencing in clinical cytogenetics: a validated approach

PDF) Low-Coverage Whole Genome Sequencing Using Laser Capture Microscopy with Combined Digital Droplet PCR: An Effective Tool to Study Copy Number and Kras Mutations in Early Lung Adenocarcinoma Development

Tumor Genome Analysis Core · GitHub

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

Frontiers Trio-Based Low-Pass Genome Sequencing Reveals Characteristics and Significance of Rare Copy Number Variants in Prenatal Diagnosis

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

Accurate quantification of copy-number aberrations and whole-genome duplications in multi-sample tumor sequencing data

Copy number profiles are stable. Ultra-low pass whole genome sequencing

Evaluation of tools for identifying large copy number variations from ultra- low-coverage whole-genome sequencing data, BMC Genomics

PDF) CNHplus: the chromosomal copy number heterogeneity which respects biological constraints