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See:
Description
| Interface Summary | |
| Allele | A single allele of a nucleotide variation. |
| AlleleConsequenceAdaptor | Adaptor for retrievning and computing AlleleConsequences. |
| AlleleFeature | An allele located on a genome. |
| AlleleGroup | Ensembl representation of a grouping of alleles (aka haplotype). |
| Genotype | Genotype. |
| Individual | This is a class representing a single individual. |
| IndividualGenotype | The genotype of a single diploid individual at a specific locus. |
| LDFeature | A linkage disequilibrium between two VariationFeatures. |
| Population | A group of individuals. |
| PopulationGenotype | A genotype that is present in a population. |
| TranscriptVariation | A TranscriptVariation object represents a variation feature which is in close proximity to an Ensembl transcript. |
| Variation | A nucleotide variation such as a SNP. |
| VariationFeature | This is a an occurrence of a nucleotide variation in the genome. |
| VariationGroup | Grouping of variations (aka haplotype set). |
| VariationGroupFeature | The point of this class is.... |
| Class Summary | |
| AlleleConsequence | Represents part or all of the effect of a single allele on a transcript. |
| ConsequenceType | TranscriptVariation consequence types. |
| LDFeatureContainer | A container for LDFeatures (linkage disequilibrium features) that provides various methods for filtering and accessing the the contained data. |
| ValidationState | Possible Validation states of a Variation. |
Data types that are unique to ensembl variation databases such as Variation, Allele and Genotype.
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