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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