| copy_number_scores | R Documentation | 
Calculate the following
Fraction of genome altered and genome doubling flag.
Fraction of genome with LOH and flag for hypoploidy.
Large-scale state transitions, see source URL.
Telomeric allelic imbalance, see source URL.
HRD-LOH score, see source URL.
calculate_fraction_cna(segs, ploidy, genome = c("hg19", "hg18", "hg38"),
  algorithm = c("em", "cncf"))
calculate_loh(segs, snps, genome = c("hg19", "hg18", "hg38"),
  algorithm = c("em", "cncf"), hypoploidy_threshold = 0.5)
calculate_ntai(segs, ploidy, genome = c("hg19", "hg18", "hg38"),
  algorithm = c("em", "cncf"), min_size = 0, min_probes = 250)
calculate_lst(segs, ploidy, genome = c("hg19", "hg18", "hg38"),
  algorithm = c("em", "cncf"), min_size = 1e+07, min_probes = 50)
calculate_hrdloh(segs, ploidy, algorithm = c("em", "cncf"))
segs | 
 FACETS segmentation output.  | 
ploidy | 
 Sample ploidy.  | 
genome | 
 Genome build.  | 
algorithm | 
 Choice between FACETS   | 
snps | 
 FACETS SNP output.  | 
hypoploidy_threshold | 
 Threshold for hypoploid call.  | 
min_size | 
 Minimum length of segment, as defined per function.  | 
min_probes | 
 Minimum number of SNPs per segment, as defined per function.  | 
List with one or more values from function.
https://www.ncbi.nlm.nih.gov/pubmed/26015868
calculate_fraction_cna(test_facets_output$segs, test_facets_output$ploidy, 'hg38', 'em') calculate_loh(test_facets_output$segs, test_facets_output$snps, 'hg38', 'em') calculate_lst(test_facets_output$segs, test_facets_output$ploidy, 'hg38', 'em') calculate_ntai(test_facets_output$segs, test_facets_output$ploidy, 'hg38', 'em') calculate_hrdloh(test_facets_output$segs, test_facets_output$ploidy, 'em')
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