NCBI C++ ToolKit
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Search Toolkit Book for NSNPVariationHelper
set of functions for dealing with SNP represented as variation objects More...
#include <objtools/snputil/snp_utils.hpp>
Public Types | |
enum | ESNPPropTypes { eSNPPropName_Undef , eSNPPropName_GeneLocation , eSNPPropName_Effect , eSNPPropName_Mapping , eSNPPropName_FreqValidation , eSNPPropName_QualityCheck , eSNPPropName_ResourceLink , eSNPPropName_ResourceLinkURL } |
enums to control getting a string list representation of various CVariantProperties More... | |
Static Public Member Functions | |
static bool | ConvertFeat (CVariation &Variation, const CSeq_feat &SrcFeat) |
legacy SNP feature conversion into a variation object More... | |
static bool | ConvertFeat (CVariation_ref &Variation, const CSeq_feat &SrcFeat) |
static void | DecodeBitfield (CVariantProperties &prop, const CSnpBitfield &bf) |
convert SNP bitfield data to respective fields in CVariantProperties More... | |
static void | VariantPropAsStrings (list< string > &ResList, const CVariantProperties &prop, ESNPPropTypes ePropType) |
get lists of strings corresponding to a given property type More... | |
template<class TVariation > | |
static void | GetDeltas (list< string > &Alleles, const TVariation *pVariation) |
add alleles to a list of strings from deltas in variation data More... | |
Static Public Attributes | |
static const string | sResourceLink_RsID |
Static Private Member Functions | |
template<class TPVariation > | |
static bool | x_CommonConvertFeat (TPVariation pVariation, const CSeq_feat &SrcFeat) |
set of functions for dealing with SNP represented as variation objects
Definition at line 249 of file snp_utils.hpp.
enums to control getting a string list representation of various CVariantProperties
Definition at line 285 of file snp_utils.hpp.
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legacy SNP feature conversion into a variation object
reads a feature that supposedly contains a SNP record (old, up-to-2012, style, with SNP data encoded as "qual" (alleles) and "ext.data" (bitfield)) and sets Variation to content found in the feature
Variation | conversion result will be put here, old contents are destroyed upon conversion success |
SrcFeat | old format feature |
Definition at line 336 of file snp_utils.cpp.
References NSnp::GetBitfield(), CSeq_feat_Base::GetLocation(), CSnpBitfield::isGood(), MSerial_AsnText, CUser_object_Base::SetClass(), CUser_field_Base::SetData(), CVariation_Base::SetExt(), CUser_object::SetField(), CVariantPlacement_Base::SetLoc(), CVariation_Base::SetPlacements(), SNP_VAR_EXT_BITFIELD, SNP_VAR_EXT_CLASS, and x_CommonConvertFeat().
Referenced by CTestBMApp::Run().
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Definition at line 359 of file snp_utils.cpp.
References NSnp::GetBitfield(), CSnpBitfield::isGood(), MSerial_AsnText, CVariation_ref::SetExt(), SNP_VAR_EXT_BITFIELD, SNP_VAR_EXT_CLASS, and x_CommonConvertFeat().
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convert SNP bitfield data to respective fields in CVariantProperties
prop | The result will be put here |
bf | Bitfield that will be decoded |
Definition at line 379 of file snp_utils.cpp.
References CSnpBitfield::e5PctMinorAllele1Plus, CSnpBitfield::e5PctMinorAlleleAll, CSnpBitfield::eAcceptor, CSnpBitfield::eDonor, CVariantProperties_Base::eEffect_frameshift, CVariantProperties_Base::eEffect_missense, CVariantProperties_Base::eEffect_stop_gain, CVariantProperties_Base::eEffect_stop_loss, CVariantProperties_Base::eEffect_synonymous, CSnpBitfield::eFrameshift, CVariantProperties_Base::eFrequency_based_validation_above_5pct_1plus, CVariantProperties_Base::eFrequency_based_validation_above_5pct_all, CVariantProperties_Base::eFrequency_based_validation_is_mutation, CVariantProperties_Base::eFrequency_based_validation_validated, CVariantProperties_Base::eGene_location_acceptor, CVariantProperties_Base::eGene_location_donor, CVariantProperties_Base::eGene_location_in_gene, CVariantProperties_Base::eGene_location_intron, CVariantProperties_Base::eGene_location_near_gene_3, CVariantProperties_Base::eGene_location_near_gene_5, CVariantProperties_Base::eGene_location_utr_3, CVariantProperties_Base::eGene_location_utr_5, CVariantProperties_Base::eGenotype_has_genotypes, CVariantProperties_Base::eGenotype_in_haplotype_set, CSnpBitfield::eHasAssemblyConflict, CSnpBitfield::eHasGenotype, CSnpBitfield::eHasGenotypeConflict, CSnpBitfield::eHasLinkOut, CSnpBitfield::eHasMemberSsConflict, CSnpBitfield::eHasOtherSameSNP, CSnpBitfield::eHasProvisionalTPA, CSnpBitfield::eHasSnp3D, CSnpBitfield::eInGene, CSnpBitfield::eInGene3, CSnpBitfield::eInGene5, CSnpBitfield::eInGenotypeKit, CSnpBitfield::eInHaplotypeSet, CSnpBitfield::eIntron, CSnpBitfield::eInUTR3, CSnpBitfield::eInUTR5, CSnpBitfield::eIsAssemblySpecific, CSnpBitfield::eIsClinical, CSnpBitfield::eIsContigAlleleAbsent, CSnpBitfield::eIsMutation, CSnpBitfield::eIsPrecious, CSnpBitfield::eIsStrainSpecific, CSnpBitfield::eIsValidated, CSnpBitfield::eIsWithdrawn, CVariantProperties_Base::eMapping_has_assembly_conflict, CVariantProperties_Base::eMapping_has_other_snp, CVariantProperties_Base::eMapping_is_assembly_specific, CSnpBitfield::eMissense, CVariantProperties_Base::eQuality_check_contig_allele_missing, CVariantProperties_Base::eQuality_check_genotype_conflict, CVariantProperties_Base::eQuality_check_non_overlapping_alleles, CVariantProperties_Base::eQuality_check_strain_specific, CVariantProperties_Base::eQuality_check_withdrawn_by_submitter, CVariantProperties_Base::eResource_link_clinical, CVariantProperties_Base::eResource_link_genotypeKit, CVariantProperties_Base::eResource_link_has3D, CVariantProperties_Base::eResource_link_preserved, CVariantProperties_Base::eResource_link_provisional, CVariantProperties_Base::eResource_link_submitterLinkout, CSnpBitfield::eStopGain, CSnpBitfield::eStopLoss, CSnpBitfield::eSynonymous, CSnpBitfield::GetVersion(), CSnpBitfield::IsTrue(), CVariantProperties_Base::SetEffect(), CVariantProperties_Base::SetFrequency_based_validation(), CVariantProperties_Base::SetGene_location(), CVariantProperties_Base::SetGenotype(), CVariantProperties_Base::SetMapping(), CVariantProperties_Base::SetQuality_check(), CVariantProperties_Base::SetResource_link(), and CVariantProperties_Base::SetVersion().
Referenced by x_CommonConvertFeat().
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add alleles to a list of strings from deltas in variation data
empty deltas are converted to dashes "-"
Alleles | list of strings to the end of which the found deltas will be added, alleles already present in the list are retained |
pVariation | variation object from which the deltas are read |
Definition at line 329 of file snp_utils.hpp.
References CSeq_literal_Base::CanGetSeq_data(), CDelta_item_Base::C_Seq::e_Literal, CDelta_item_Base::C_Seq::e_This, CAliasBase< TPrim >::Get(), CSeq_data_Base::GetIupacaa(), CSeq_data_Base::GetIupacna(), CDelta_item_Base::C_Seq::GetLiteral(), CSeq_literal_Base::GetSeq_data(), CSeq_data_Base::IsIupacaa(), CSeq_data_Base::IsIupacna(), ITERATE, and CDelta_item_Base::C_Seq::Which().
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get lists of strings corresponding to a given property type
ResList | will be reset to the resulting list of strings |
prop | property based upon values within which the result will be generated |
ePropType | type of property requested |
Definition at line 536 of file snp_utils.cpp.
References CVariantProperties_Base::CanGetEffect(), CVariantProperties_Base::CanGetFrequency_based_validation(), CVariantProperties_Base::CanGetGene_location(), CVariantProperties_Base::CanGetMapping(), CVariantProperties_Base::CanGetQuality_check(), CVariantProperties_Base::CanGetResource_link(), CVariantProperties_Base::eEffect_down_regulator, CVariantProperties_Base::eEffect_frameshift, CVariantProperties_Base::eEffect_methylation, CVariantProperties_Base::eEffect_missense, CVariantProperties_Base::eEffect_no_change, CVariantProperties_Base::eEffect_nonsense, CVariantProperties_Base::eEffect_stop_gain, CVariantProperties_Base::eEffect_stop_loss, CVariantProperties_Base::eEffect_synonymous, CVariantProperties_Base::eEffect_up_regulator, CVariantProperties_Base::eFrequency_based_validation_above_1pct_1plus, CVariantProperties_Base::eFrequency_based_validation_above_1pct_all, CVariantProperties_Base::eFrequency_based_validation_above_5pct_1plus, CVariantProperties_Base::eFrequency_based_validation_above_5pct_all, CVariantProperties_Base::eFrequency_based_validation_is_mutation, CVariantProperties_Base::eFrequency_based_validation_validated, CVariantProperties_Base::eGene_location_acceptor, CVariantProperties_Base::eGene_location_conserved_noncoding, CVariantProperties_Base::eGene_location_donor, CVariantProperties_Base::eGene_location_in_gene, CVariantProperties_Base::eGene_location_in_start_codon, CVariantProperties_Base::eGene_location_in_stop_codon, CVariantProperties_Base::eGene_location_intergenic, CVariantProperties_Base::eGene_location_intron, CVariantProperties_Base::eGene_location_near_gene_3, CVariantProperties_Base::eGene_location_near_gene_5, CVariantProperties_Base::eGene_location_utr_3, CVariantProperties_Base::eGene_location_utr_5, CVariantProperties_Base::eMapping_has_assembly_conflict, CVariantProperties_Base::eMapping_has_other_snp, CVariantProperties_Base::eMapping_is_assembly_specific, CVariantProperties_Base::eQuality_check_contig_allele_missing, CVariantProperties_Base::eQuality_check_genotype_conflict, CVariantProperties_Base::eQuality_check_non_overlapping_alleles, CVariantProperties_Base::eQuality_check_strain_specific, CVariantProperties_Base::eQuality_check_withdrawn_by_submitter, CVariantProperties_Base::eResource_link_clinical, CVariantProperties_Base::eResource_link_genotypeKit, CVariantProperties_Base::eResource_link_has3D, CVariantProperties_Base::eResource_link_preserved, CVariantProperties_Base::eResource_link_provisional, CVariantProperties_Base::eResource_link_submitterLinkout, eSNPPropName_Effect, eSNPPropName_FreqValidation, eSNPPropName_GeneLocation, eSNPPropName_Mapping, eSNPPropName_QualityCheck, eSNPPropName_ResourceLink, eSNPPropName_ResourceLinkURL, CVariantProperties_Base::GetEffect(), CVariantProperties_Base::GetFrequency_based_validation(), CVariantProperties_Base::GetGene_location(), CVariantProperties_Base::GetMapping(), CVariantProperties_Base::GetQuality_check(), and CVariantProperties_Base::GetResource_link().
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Definition at line 379 of file snp_utils.hpp.
References DecodeBitfield(), CSnpBitfield::eDips, CSnpBitfield::eMicrosatellite, CSnpBitfield::eMultiBase, CVariation_ref::eSeqType_na, CSnpBitfield::eSingleBase, CVariation_inst_Base::eType_other, NSnp::GetAlleles(), NSnp::GetBitfield(), CVariation_ref_Base::GetData(), CVariation_ref_Base::C_Data::GetInstance(), NSnp::GetRsid(), NSnp::GetTag(), CSnpBitfield::GetVariationClass(), CSnpBitfield::isGood(), CVariation_ref_Base::C_Data::IsInstance(), NSnp::IsSnp(), NStr::Join(), CVariation_ref_Base::SetData(), CVariation_ref::SetDeletionInsertion(), CVariation_ref::SetMNP(), and CVariation_ref::SetSNV().
Referenced by ConvertFeat().
Definition at line 281 of file snp_utils.hpp.