ensembl-variation | Top |
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ensembl-variation::C_code | Top |
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ensembl-variation::documentation | Top |
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ensembl-variation::modules | Top |
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ensembl-variation::modules::Bio | Top |
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ensembl-variation::modules::Bio::EnsEMBL | Top |
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ensembl-variation::modules::Bio::EnsEMBL::Variation | Top |
Allele | A single allele of a nucleotide variation. |
AlleleFeature | A genomic position for an allele in a sample. |
AlleleGroup | Ensembl representation of a grouping of alleles (aka haplotype). |
ConsequenceType | Bio::EnsEMBL::Variation::ConsequenceType |
Genotype | Abstract base class representing a genotype |
Individual | A single member of a population. |
IndividualGenotype | Module representing the genotype of a single individual at a single position |
IndividualGenotypeFeature | Module representing the genotype of a single individual at a single position |
LDFeatureContainer | A container with all the ld values for quick access |
Population | A population represents a phenotypic group, ethnic group, set of individuals used in an assay, etc. |
PopulationGenotype | Module for a genotype represented in a population. |
ReadCoverage | A coverage reagion for a read. |
ReadCoverageCollection | A collection of coverage reagion for a read. |
Sample | An abstract base class to represent Population, Individual or Strain |
TranscriptVariation | Bio::EnsEMBL::Variation::TranscriptVariation |
Variation | Ensembl representation of a nucleotide variation. |
VariationAnnotation | A genotype phenotype annotation for a nucleotide variation. |
VariationFeature | A genomic position for a nucleotide variation. |
VariationGroup | Ensembl representation of a grouping of variations (aka haplotype set). |
VariationGroupFeature | A genomic position for a variation group (aka haplotype block). |
ensembl-variation::modules::Bio::EnsEMBL::Variation::DBSQL | Top |
AlleleFeatureAdaptor | Bio::EnsEMBL::Variation::DBSQL::AlleleFeatureAdaptor |
AlleleGroupAdaptor | Bio::EnsEMBL::Variation::DBSQL::AlleleGroupAdaptor |
BaseGenotypeAdaptor | Bio::EnsEMBL::Variation::DBSQL::BaseGenotypeAdaptor |
CompressedGenotypeAdaptor | Bio::EnsEMBL::Variation::DBSQL::CompressedGenotypeAdaptor |
DBAdaptor | Bio::EnsEMBL::DBSQL::DBAdaptor |
IndividualAdaptor | Bio::EnsEMBL::DBSQL::IndividualAdaptor |
IndividualGenotypeAdaptor | Bio::EnsEMBL::Variation::DBSQL::IndividualGenotypeAdaptor |
LDFeatureContainerAdaptor | Bio::EnsEMBL::Variation::DBSQL::LDFeatureContainerAdaptor |
MetaContainer | Encapsulates all access to variation database meta information |
PopulationAdaptor | Bio::EnsEMBL::Variation::DBSQL::PopulationAdaptor |
PopulationGenotypeAdaptor | Bio::EnsEMBL::Variation::DBSQL::PopulationGenotypeAdaptor |
ReadCoverageAdaptor | Bio::EnsEMBL::Variation::DBSQL::ReadCoverageAdaptor |
ReadCoverageCollectionAdaptor | Bio::EnsEMBL::Variation::DBSQL::ReadCoverageCollectionAdaptor |
SampleAdaptor | Bio::EnsEMBL::Variation::DBSQL::SampleAdaptor |
TranscriptVariationAdaptor | Bio::EnsEMBL::Variation::DBSQL::TranscriptVariationAdaptor |
VariationAdaptor | Bio::EnsEMBL::Variation::DBSQL::VariationAdaptor |
VariationAnnotationAdaptor | Bio::EnsEMBL::Variation::DBSQL::VariationAnnotationAdaptor |
VariationFeatureAdaptor | Bio::EnsEMBL::Variation::DBSQL::VariationFeatureAdaptor |
VariationGroupAdaptor | Bio::EnsEMBL::Variation::DBSQL::VariationGroupAdaptor |
VariationGroupFeatureAdaptor | Bio::EnsEMBL::Variation::DBSQL::VariationGroupFeatureAdaptor |
ensembl-variation::modules::Bio::EnsEMBL::Variation::Utils | Top |
Sequence | Utility functions for sequences |
ensembl-variation::modules::t | Top |
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ensembl-variation::modules::t::test-genome-DBs | Top |
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ensembl-variation::modules::t::test-genome-DBs::homo_sapiens | Top |
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ensembl-variation::modules::t::test-genome-DBs::homo_sapiens::core | Top |
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ensembl-variation::modules::t::test-genome-DBs::homo_sapiens::variation | Top |
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ensembl-variation::schema | Top |
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ensembl-variation::scripts | Top |
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ensembl-variation::scripts::import | Top |
DBH | |
ImportUtils |
ensembl-variation::scripts::import::LRG | Top |
LRG(1) | |
LRG(2) | |
Node |
ensembl-variation::scripts::import::SARA | Top |
GetSARA |
ensembl-variation::scripts::import::Sanger | Top |
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ensembl-variation::scripts::import::Solexa | Top |
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ensembl-variation::scripts::import::dbSNP | Top |
GenericChromosome | |
GenericContig | |
Human | |
MappingChromosome | |
Mosquito |
ensembl-variation::scripts::ssahaSNP | Top |
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ensembl-variation::sql | Top |