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

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

PDF) WAVECNV: A New Approach for Detecting Copy Number Variation by Wavelet Clustering

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

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

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

PDF) Oral cancer prediction by noninvasive genetic screening

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

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

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

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

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

Low-Pass Whole Genome Sequencing