Nothing
globalVariables(unique(c(
# af_distribution:
"minorfreq",
# arrange_data:
"ALT", "ALT_COUNT", "ALT_FREQ", "ALT_TYPE", "ANN", "CHROM", "gt_AD", "major", "majorcount", "majorfreq", "minor", "minorcount", "minorfreq", "POS", "REF", "REF_COUNT", "REF_FREQ",
# dNdS_segment:
"annotation", "dNdS", "feature_id", "n.x", "n.y", "SPLICEFORMS",
# filter_variants:
"ALT_FREQ", "ALT_FREQ.x", "ALT_FREQ.y", "gt_DP", "gt_DP.x", "gt_DP.y",
# plot_shannon:
"CHROM", "genome_shannon_perkb", "POS", "shannon_chrom_perkb", "shannon_ntpos",
# position_allele_freq:
"CHROM", "major", "majorfreq", "minor", "minorfreq", "POS",
# prepare_annotations:
"ANN",
# read_reference_fasta_dna:
"CHROM", "CHROM_SIZE", "V1",
# shannon_entropy:
"CHROM", "chrom_shannon", "SegmentSize", "shannon_ntpos",
# shared_snv_plot:
"CHROM", "count", "DF_filt", "POS", "totalsamp", "variant",
# shared_snv_table:
"ALT", "annotation", "CHROM", "count", "feature_id", "feature_type", "HGVS.p", "major", "majorfreq", "minor", "minorfreq", "POS", "protein_position", "REF", "totalsamp", "variant",
# snv_genome:
"annotation", "n",
# snv_location:
"ALT_TYPE", "major", "majorfreq", "minor", "minorfreq", "POS",
# snv_segment:
"annotation", "CHROM", "n",
# tstv_plot:
".", "chrom_or_genome", "tstv_ratio_perkb",
# tstv_ratio:
"tstv", "tstv_chrom_count"
)))
Any scripts or data that you put into this service are public.
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.