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- aggregations
- assets
- images
- javascripts
- lunr
- min
- workers
- stylesheets
- beacon-flavours
- changes-todo
- code-organization
- contribute
- css
- filters
- formats-standards
- framework
- handovers
- img
- Beacon-Networks-v2-graphics
- implementations-options
- implementations/org.progenetix
- models
- networks
- other-implementations
- pedigree
- records
- requests
- requestParameterComponents
- requestProfiles_g_variant
- rest-api
- schemas-md
- analyses_defaultSchema
- beacon_terms
- biosamples_defaultSchema
- cohorts_defaultSchema
- datasets_defaultSchema
- genomicVariations_defaultSchema
- individuals_defaultSchema
- obj
- AgeRange_PXF
- Age
- Allele
- Complex Value
- CopyNumber
- GestationalAge
- Haplotype
- LegacyVariation
- MolecularVariation
- SystemicVariation
- TimeInterval
- Value_PXF
- affected
- ageAtExposure
- ageAtOnset
- ageAtProcedure
- ageOfOnset
- ageRange
- aligner
- alleleFrequency
- alleleOrigin
- alternateBases
- aminoacidChanges
- analysisDate
- analysisId
- annotatedWith
- assayCode
- availabilityCount
- availability
- biosampleId
- biosampleStatus
- bodySite
- caseLevelData
- category
- clinicalInterpretations
- clinicalRelevance
- clinvarVariantId
- cohortDataTypes
- cohortDesign
- cohortSize
- cohortType
- collectionDate
- collectionEvents
- collectionMoment
- conditionId
- createDateTime
- cumulativeDose
- dataUseConditions
- dateOfProcedure
- date
- description
- diagnosticMarkers
- diseaseCode
- diseaseConditions
- diseases
- disease
- distribution
- doseIntervals
- duoDataUse
- duration
- effect
- end
- ethnicities
- ethnicity
- eventAgeRange
- eventCases
- eventControls
- eventDataTypes
- eventDate
- eventDiseases
- eventEthnicities
- eventGenders
- eventLocations
- eventNum
- eventPhenotypes
- eventSize
- eventTimeline
- evidenceCode
- evidenceType
- evidence
- excluded
- exclusionCriteria
- exposureCode
- exposures
- externalUrl
- familyHistory
- featureClass
- featureID
- featureType
- frequencies
- frequencyInPopulations
- genders
- geneIds
- genomicFeatures
- genomicHGVSId
- geographicOrigin
- histologicalDiagnosis
- identifiers
- id
- inclusionCriteria
- individualId
- info
- interval
- interventionsOrProcedures
- iso8601duration
- karyotypicSex
- label
- libraryLayout
- librarySelection
- librarySource
- libraryStrategy
- locations
- location
- measurementValue
- measurements
- measures
- memberId
- members
- modifiers
- molecularAttributes
- molecularEffects
- name
- notes
- numSubjects
- observationMoment
- obtentionProcedure
- onset
- pathologicalStage
- pathologicalTnmFinding
- pedigrees
- phenotypicConditions
- phenotypicEffects
- phenotypicFeatures
- pipelineName
- pipelineRef
- platformModel
- platform
- population
- procedureCode
- procedure
- proteinHGVSIds
- quantity
- referenceBases
- referenceRange
- reference
- resolution
- role
- routeOfAdministration
- runDate
- runId
- sampleOriginDetail
- sampleOriginType
- sampleProcessing
- sampleStorage
- scheduleFrequency
- severity
- sex
- sourceReference
- source
- stage
- start
- toolName
- toolReferences
- transcriptHGVSIds
- treatmentCode
- treatments
- tumorGrade
- tumorProgression
- unit
- updateDateTime
- value
- variantAlternativeIds
- variantCaller
- variantInternalId
- variantLevelData
- variantType
- variation
- version
- zygosity
- runs_defaultSchema
- search
- security
- variant-queries
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