ploidy and copy number states very different between SNParray (ASCAT) and WGS (FACETS) · Issue #113 · mskcc/facets · GitHub
facets plot interpretation · Issue #133 · mskcc/facets · GitHub
hsegHMM: hidden Markov model-based allele-specific copy number alteration analysis accounting for hypersegmentation | BMC Bioinformatics | Full Text
Copy number estimates from FACETS for Patient 1. A decrease in copy... | Download Scientific Diagram
159 Free Copy Number Variation (CNV) Analysis Tools - Software and Resources
![PDF] FACETS: allele-specific copy number and clonal heterogeneity analysis tool for high-throughput DNA sequencing | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/0333c81df745873f6cadadb6009446166eea7136/5-Figure4-1.png "PDF] FACETS: allele-specific copy number and clonal heterogeneity analysis tool for high-throughput DNA sequencing | Semantic Scholar")
PDF] FACETS: allele-specific copy number and clonal heterogeneity analysis tool for high-throughput DNA sequencing | Semantic Scholar
What's new in FacetWP 4.0 | FacetWP
JMP | Free Full-Text | Analysis of Copy Number Variations in Solid Tumors Using a Next Generation Sequencing Custom Panel
Copy number signature analysis tool and its application in prostate cancer reveals distinct mutational processes and clinical outcomes | PLOS Genetics
![PDF] FACETS: allele-specific copy number and clonal heterogeneity analysis tool for high-throughput DNA sequencing | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/0333c81df745873f6cadadb6009446166eea7136/2-Figure1-1.png "PDF] FACETS: allele-specific copy number and clonal heterogeneity analysis tool for high-throughput DNA sequencing | Semantic Scholar")
PDF] FACETS: allele-specific copy number and clonal heterogeneity analysis tool for high-throughput DNA sequencing | Semantic Scholar
Detection of Biallelic Loss of DNA Repair Genes in Formalin-Fixed, Paraffin-Embedded Tumor Samples Using a Novel Tumor-Only Sequencing Panel - The Journal of Molecular Diagnostics
FACETS: Fraction and Allele-Specific Copy Number Estimates from Tumor Sequencing | SpringerLink
Diversity of Prdm9 Zinc Finger Array in Wild Mice Unravels New Facets of the Evolutionary Turnover of this Coding Minisatellite | PLOS ONE
Copy number signatures predict chromothripsis and clinical outcomes in newly diagnosed multiple myeloma | Nature Communications
Figure 7 from FACETS: allele-specific copy number and clonal heterogeneity analysis tool for high-throughput DNA sequencing | Semantic Scholar
PureCN: copy number calling and SNV classification using targeted short read sequencing | Source Code for Biology and Medicine | Full Text
Global diversity, population stratification, and selection of human copy- number variation | Science
ploidy and copy number states very different between SNParray (ASCAT) and WGS (FACETS) · Issue #113 · mskcc/facets · GitHub
Comprehensive Assessment of Somatic Copy Number Variation Calling Using Next-Generation Sequencing Data | bioRxiv
Accurate quantification of copy-number aberrations and whole-genome duplications in multi-sample tumor sequencing data | Nature Communications
smoothing of logR and logOR before segmentation · Issue #102 · mskcc/facets · GitHub
Filtering and interpreting results · Issue #62 · mskcc/facets · GitHub
FACETS: Fraction and Allele-Specific Copy Number Estimates from Tumor Sequencing | SpringerLink
PDF) FACETS: Allele-specific copy number and clonal heterogeneity analysis tool for high-throughput DNA sequencing
