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

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

GitHub - DKFZ-ODCF/ACEseqWorkflow: Allele-specific copy number estimation with whole genome sequencing

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

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

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

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

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

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

Diagnostics, Free Full-Text

Computational validation of clonal and subclonal copy number alterations from bulk tumor sequencing using CNAqc, Genome Biology

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

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

DNA copy number profiling: from bulk tissue to single cells

Understanding and increasing coverage : Knowledge Base

The variables for NGS experiments: coverage, read length, multiplexing

Extremely low-coverage sequencing and imputation increases power for genome-wide association studies

Experts report record low Great Lakes ice coverage

Low-pass sequencing and imputation for evaluating genetic