R Packages that start with:
A . B . C . D . E . F . G . H . I . J . K . L . M . N . O . P . Q . R . S . T . U . V . W . X . Y . Z .
Functions
- add_object_tier()
- allele_name()
- ancestral_groups_tbl()
- ancestries_tbl()
- associations-class()
- associations()
- associations_drop_na()
- associations_tbl()
- association_to_study()
- association_to_trait()
- association_to_variant()
- bind()
- child_efo_ids()
- contains_question_mark()
- countries_tbl()
- cytogenetic_bands()
- cytogenetic_band_to_genomic_range()
- empty_to_na()
- ensembl_ids_tbl()
- entrez_ids_tbl()
- equal_length()
- exists_variant()
- extract_association_id()
- filter_by_id()
- filter_variants_by_standard_chromosomes()
- gc_examples()
- gc_get()
- gc_request()
- gc_request_all()
- genomic_contexts_tbl()
- genotyping_techs_tbl()
- get_associations()
- get_associations_all()
- get_associations_by_association_id()
- get_associations_by_efo_id()
- get_associations_by_efo_trait()
- get_associations_by_pubmed_id()
- get_associations_by_study_id()
- get_associations_by_variant_id()
- get_child_efo()
- get_metadata()
- get_studies()
- get_studies_all()
- get_studies_by_association_id()
- get_studies_by_efo_id()
- get_studies_by_efo_trait()
- get_studies_by_efo_uri()
- get_studies_by_full_pvalue_set()
- get_studies_by_pubmed_id()
- get_studies_by_reported_trait()
- get_studies_by_study_id()
- get_studies_by_user_requested()
- get_studies_by_variant_id()
- get_traits()
- get_traits_all()
- get_traits_by_association_id()
- get_traits_by_efo_id()
- get_traits_by_efo_trait()
- get_traits_by_efo_uri()
- get_traits_by_pubmed_id()
- get_traits_by_study_id()
- get_variants()
- get_variants_all()
- get_variants_by_association_id()
- get_variants_by_cytogenetic_band()
- get_variants_by_efo_id()
- get_variants_by_efo_trait()
- get_variants_by_gene_name()
- get_variants_by_genomic_range()
- get_variants_by_pubmed_id()
- get_variants_by_reported_trait()
- get_variants_by_study_id()
- get_variants_by_variant_id()
- gwasrapidd-package()
- is_association_id()
- is_ebi_reachable()
- is_efo_id()
- is_efo_id2()
- is_embedded()
- is_empty_str()
- is_human_chromosome()
- is_paginated()
- is_pubmed_id()
- is_rs_id()
- is_study_id()
- list_to_s4()
- loci_tbl()
- lstjoin()
- metadata_lst()
- missing_to_na()
- n()
- normalise_obj()
- object_type_from_url()
- open_in_dbsnp()
- open_in_gtex()
- open_in_gwas_catalog()
- open_in_pubmed()
- peel_off_embedded()
- pipe()
- platforms_tbl()
- publications_tbl()
- recursive_apply()
- reported_genes_tbl()
- risk_alleles_tbl()
- s4_to_list()
- setop()
- set_testing_fast()
- set_testing_slow()
- skip_if_testing_is_fast()
- studies-class()
- studies()
- studies_drop_na()
- studies_tbl()
- study_to_association()
- study_to_trait()
- study_to_variant()
- subset-associations()
- subset-studies()
- subset-traits()
- subset-variants()
- sure()
- traits-class()
- traits()
- traits_drop_na()
- traits_tbl()
- trait_to_association()
- trait_to_study()
- trait_to_variant()
- tws()
- variants-class()
- variants()
- variants_drop_na()
- variants_tbl()
- variant_name()
- variant_to_association()
- variant_to_study()
- variant_to_trait()
- v_ensembl_ids_tbl()
- v_entrez_ids_tbl()
- write_xlsx()
R Codes
- browser.R
- class-associations.R
- class-studies.R
- class-traits.R
- class-variants.R
- data.R
- ebi_server.R
- generics.R
- get_associations.R
- get_metadata.R
- get_studies.R
- get_traits.R
- get_variants.R
- gwasrapidd-package.R
- id_mapping.R
- list_joins.R
- missing.R
- parse-associations.R
- parse-studies.R
- parse-traits.R
- parse-utils.R
- parse-variants.R
- post-studies.R
- post-traits.R
- post-variants.R
- recursive_apply.R
- request.R
- s4-utils.R
- sure.R
- tests.R
- utils-pipe.R
- utils.R
- write_xlsx.R
Selected R package: gwasrapidd
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