Global functions | |
---|---|
SYNDROMES | Man page |
all_enrichment | Man page Source code |
analyse_inherited_enrichment | Man page Source code |
biallelic_func_enrichment | Man page Source code |
biallelic_lof_enrichment | Man page Source code |
biallelic_syn_enrichment | Man page Source code |
calculate_gene_similarity | Man page Source code |
calculate_no_match | Man page Source code |
calculate_proband_similarity | Man page Source code |
calculate_syndrome_rates | Man page Source code |
check_autozygosity_in_chrom | Man page Source code |
check_for_last_base_in_exon | Man page Source code |
check_sample_autozygosity_genome_wide | Man page Source code |
convert_genotypes | Man page Source code |
cumulative_frequency | Man page Source code |
enrichment_multiple_populations | Man page Source code |
enrichment_single_population | Man page Source code |
filter_exac_variants_by_cadd | Man page Source code |
find_file_pos | Man page Source code |
gencode | Man page |
get_count_combinations | Man page Source code |
get_cumulative_frequencies | Man page Source code |
get_ddd_cohort | Man page Source code |
get_ddd_variants_for_gene | Man page Source code |
get_ddd_vep_annotations | Man page Source code |
get_exac_variants_for_gene | Man page Source code |
get_exon_ends | Man page Source code |
get_gene_coordinates | Man page Source code |
get_gene_ids_for_hgnc | Man page Source code |
get_hemizygous | Man page Source code |
get_lines_from_vep_vcf | Man page Source code |
get_list_of_population_frequencies | Man page Source code |
get_most_severe_consequence | Man page Source code |
get_polyphen | Man page Source code |
get_transcript_ids_for_ensembl_gene_ids | Man page Source code |
lof_func_enrichment | Man page Source code |
open_suspected_syndromes | Man page Source code |
parse_vep_output | Man page Source code |
permute_probands | Man page Source code |
recessiveStats | Man page |
recessiveStats-package | Man page |
reformat_chrX_genotypes | Man page Source code |
remove_easy_nonfunctional | Man page Source code |
remove_high_frequency_vars | Man page Source code |
remove_nonfunctional_variants | Man page Source code |
request_from_ensembl | Man page Source code |
set_exac_path | Man page Source code |
standardise_multiple_alt_variants | Man page Source code |
sum_combo_tests | Man page Source code |
tally_alleles | Man page Source code |
test_gene | Man page Source code |
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