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use std::str::FromStr;
use super::ParseError;
/// A VCF header info key.
#[derive(Clone, Copy, Debug, Eq, Hash, PartialEq)]
pub enum Standard {
/// Ancestral allele (`AA`).
AncestralAllele,
/// Allele count in genotypes, for each ALT allele, in the same order as listed (`AC`).
AlleleCount,
/// Total read depth for each allele (`AD`).
TotalReadDepths,
/// Read depth for each allele on the forward strand (`ADF`).
ForwardStrandReadDepths,
/// Read depth for each allele on the reverse strand (`ADR`).
ReverseStrandReadDepths,
/// Allele frequency for each ALT allele in the same order as listed (`AF`).
AlleleFrequencies,
/// Total number of alleles in called genotypes (`AN`).
TotalAlleleCount,
/// RMS base quality (`BQ`).
BaseQuality,
/// Cigar string describing how to align an alternate allele to the reference allele (`CIGAR`).
Cigar,
/// dbSNP membership (`DB`).
IsInDbSnp,
/// Combined depth across samples (`DP`).
TotalDepth,
// /// End position on CHROM (`END`).
// EndPosition,
/// HapMap2 membership (`H2`).
IsInHapMap2,
/// HapMap3 membership (`H3`).
IsInHapMap3,
/// RMS mapping quality (`MQ`).
MappingQuality,
/// Number of MAPQ == 0 reads (`MQ0`).
ZeroMappingQualityCount,
/// Number of samples with data (`NS`).
SamplesWithDataCount,
/// Strand bias (`SB`).
StrandBias,
/// Somatic mutation (`SOMATIC`).
IsSomaticMutation,
/// Validated by follow-up experiment (`VALIDATED`).
IsValidated,
/// 1000 Genomes membership (`1000G`).
IsIn1000Genomes,
/// Imprecise structural variation (`IMPRECISE`).
IsImprecise,
/// Indicates a novel structural variation (`NOVEL`).
IsNovel,
/// End position of the variant described in this record (`END`).
EndPosition,
/// Type of structural variant (`SVTYPE`).
///
/// Deprecated in VCF 4.4.
SvType,
/// Difference in length between REF and ALT alleles (`SVLEN`).
SvLengths,
/// Confidence interval around POS for imprecise variants (`CIPOS`).
PositionConfidenceIntervals,
/// Confidence interval around END for imprecise variants (`CIEND`).
EndConfidenceIntervals,
/// Length of base pair identical micro-homology at event breakpoints (`HOMLEN`).
MicrohomologyLengths,
/// Sequence of base pair identical micro-homology at event breakpoints (`HOMSEQ`).
MicrohomologySequences,
/// ID of the assembled alternate allele in the assembly file (`BKPTID`).
BreakpointIds,
/// Mobile element info of the form NAME,START,END,POLARITY (`MEINFO`).
MobileElementInfo,
/// Mobile element transduction info of the form CHR,START,END,POLARITY (`METRANS`).
MobileElementTransductionInfo,
/// ID of this element in Database of Genomic Variation (`DBVID`).
DbvId,
/// ID of this element in DBVAR (`DBVARID`).
DbVarId,
/// ID of this element in DBRIP (`DBRIPID`).
DbRipId,
/// ID of mate breakends (`MATEID`).
MateBreakendIds,
/// ID of partner breakend (`PARID`).
PartnerBreakendId,
/// ID of event associated to breakend (`EVENT`).
BreakendEventId,
/// ID of associated event (`EVENTTYPE`).
///
/// Added in VCF 4.4.
EventType,
/// Confidence interval around the inserted material between breakends (`CILEN`).
BreakendConfidenceIntervals,
// /// Read Depth of segment containing breakend (`DP`).
// BreakendReadDepth,
/// Read Depth of adjacency (`DPADJ`).
///
/// Removed in VCF 4.4.
AdjacentReadDepths,
/// Copy number of segment containing breakend (`CN`).
BreakendCopyNumber,
/// Copy number of adjacency (`CNADJ`).
///
/// Removed in VCF 4.4.
AdjacentCopyNumber,
/// Confidence interval around copy number for the segment (`CICN`).
CopyNumberConfidenceIntervals,
/// Confidence interval around copy number for the adjacency (`CICNADJ`).
///
/// Removed in VCF 4.4.
AdjacentCopyNumberConfidenceIntervals,
/// Claim made by the structural variant call. Valid values are D, J, DJ for abundance,
/// adjacency and both respectively.
///
/// Added in VCF 4.4.
SvClaim,
/// Total number of repeat sequences in this allele (`RN`).
///
/// Added in VCF 4.4.
TotalRepeatSequenceCounts,
/// Repeat unit sequence of the corresponding repeat sequence (`RUS`).
///
/// Added in VCF 4.4.
RepeatUnitSequences,
/// Repeat unit length of the corresponding repeat sequence (`RUL`).
///
/// Added in VCF 4.4.
RepeatUnitLengths,
/// Repeat unit count of corresponding repeat sequence (`RUC`).
///
/// Added in VCF 4.4.
RepeatUnitCounts,
/// Total number of bases in the corresponding repeat sequence (`RB`).
///
/// Added in VCF 4.4.
TotalRepeatSequenceBaseCounts,
/// Confidence interval around RUC (`CIRUC`).
///
/// Added in VCF 4.4.
RepeatUnitCountConfidenceIntervals,
/// Confidence interval around RB (`CIRB`).
///
/// Added in VCF 4.4.
TotalRepeatSequenceBaseCountConfidenceIntervals,
/// Number of bases in each individual repeat unit (`RUB`).
///
/// Added in VCF 4.4.
RepeatUnitBaseCounts,
}
impl AsRef<str> for Standard {
fn as_ref(&self) -> &str {
match self {
Self::AncestralAllele => "AA",
Self::AlleleCount => "AC",
Self::TotalReadDepths => "AD",
Self::ForwardStrandReadDepths => "ADF",
Self::ReverseStrandReadDepths => "ADR",
Self::AlleleFrequencies => "AF",
Self::TotalAlleleCount => "AN",
Self::BaseQuality => "BQ",
Self::Cigar => "CIGAR",
Self::IsInDbSnp => "DB",
Self::TotalDepth => "DP",
// Self::EndPosition => "END",
Self::IsInHapMap2 => "H2",
Self::IsInHapMap3 => "H3",
Self::MappingQuality => "MQ",
Self::ZeroMappingQualityCount => "MQ0",
Self::SamplesWithDataCount => "NS",
Self::StrandBias => "SB",
Self::IsSomaticMutation => "SOMATIC",
Self::IsValidated => "VALIDATED",
Self::IsIn1000Genomes => "1000G",
Self::IsImprecise => "IMPRECISE",
Self::IsNovel => "NOVEL",
Self::EndPosition => "END",
Self::SvType => "SVTYPE",
Self::SvLengths => "SVLEN",
Self::PositionConfidenceIntervals => "CIPOS",
Self::EndConfidenceIntervals => "CIEND",
Self::MicrohomologyLengths => "HOMLEN",
Self::MicrohomologySequences => "HOMSEQ",
Self::BreakpointIds => "BKPTID",
Self::MobileElementInfo => "MEINFO",
Self::MobileElementTransductionInfo => "METRANS",
Self::DbvId => "DGVID",
Self::DbVarId => "DBVARID",
Self::DbRipId => "DBRIPID",
Self::MateBreakendIds => "MATEID",
Self::PartnerBreakendId => "PARID",
Self::BreakendEventId => "EVENT",
Self::EventType => "EVENTTYPE",
Self::BreakendConfidenceIntervals => "CILEN",
// Self::BreakendReadDepth => "DP",
Self::AdjacentReadDepths => "DPADJ",
Self::BreakendCopyNumber => "CN",
Self::AdjacentCopyNumber => "CNADJ",
Self::CopyNumberConfidenceIntervals => "CICN",
Self::AdjacentCopyNumberConfidenceIntervals => "CICNADJ",
Self::SvClaim => "SVCLAIM",
Self::TotalRepeatSequenceCounts => "RN",
Self::RepeatUnitSequences => "RUS",
Self::RepeatUnitLengths => "RUL",
Self::RepeatUnitCounts => "RUC",
Self::TotalRepeatSequenceBaseCounts => "RB",
Self::RepeatUnitCountConfidenceIntervals => "CIRUC",
Self::TotalRepeatSequenceBaseCountConfidenceIntervals => "CIRB",
Self::RepeatUnitBaseCounts => "RUB",
}
}
}
impl FromStr for Standard {
type Err = ParseError;
fn from_str(s: &str) -> Result<Self, Self::Err> {
match s {
"AA" => Ok(Self::AncestralAllele),
"AC" => Ok(Self::AlleleCount),
"AD" => Ok(Self::TotalReadDepths),
"ADF" => Ok(Self::ForwardStrandReadDepths),
"ADR" => Ok(Self::ReverseStrandReadDepths),
"AF" => Ok(Self::AlleleFrequencies),
"AN" => Ok(Self::TotalAlleleCount),
"BQ" => Ok(Self::BaseQuality),
"CIGAR" => Ok(Self::Cigar),
"DB" => Ok(Self::IsInDbSnp),
"DP" => Ok(Self::TotalDepth),
// "END" => Ok(Self::EndPosition),
"H2" => Ok(Self::IsInHapMap2),
"H3" => Ok(Self::IsInHapMap3),
"MQ" => Ok(Self::MappingQuality),
"MQ0" => Ok(Self::ZeroMappingQualityCount),
"NS" => Ok(Self::SamplesWithDataCount),
"SB" => Ok(Self::StrandBias),
"SOMATIC" => Ok(Self::IsSomaticMutation),
"VALIDATED" => Ok(Self::IsValidated),
"1000G" => Ok(Self::IsIn1000Genomes),
"IMPRECISE" => Ok(Self::IsImprecise),
"NOVEL" => Ok(Self::IsNovel),
"END" => Ok(Self::EndPosition),
"SVTYPE" => Ok(Self::SvType),
"SVLEN" => Ok(Self::SvLengths),
"CIPOS" => Ok(Self::PositionConfidenceIntervals),
"CIEND" => Ok(Self::EndConfidenceIntervals),
"HOMLEN" => Ok(Self::MicrohomologyLengths),
"HOMSEQ" => Ok(Self::MicrohomologySequences),
"BKPTID" => Ok(Self::BreakpointIds),
"MEINFO" => Ok(Self::MobileElementInfo),
"METRANS" => Ok(Self::MobileElementTransductionInfo),
"DGVID" => Ok(Self::DbvId),
"DBVARID" => Ok(Self::DbVarId),
"DBRIPID" => Ok(Self::DbRipId),
"MATEID" => Ok(Self::MateBreakendIds),
"PARID" => Ok(Self::PartnerBreakendId),
"EVENT" => Ok(Self::BreakendEventId),
"EVENTTYPE" => Ok(Self::EventType),
"CILEN" => Ok(Self::BreakendConfidenceIntervals),
// "DP" => Ok(Self::BreakendReadDepth),
"DPADJ" => Ok(Self::AdjacentReadDepths),
"CN" => Ok(Self::BreakendCopyNumber),
"CNADJ" => Ok(Self::AdjacentCopyNumber),
"CICN" => Ok(Self::CopyNumberConfidenceIntervals),
"CICNADJ" => Ok(Self::AdjacentCopyNumberConfidenceIntervals),
"SVCLAIM" => Ok(Self::SvClaim),
"RN" => Ok(Self::TotalRepeatSequenceCounts),
"RUS" => Ok(Self::RepeatUnitSequences),
"RUL" => Ok(Self::RepeatUnitLengths),
"RUC" => Ok(Self::RepeatUnitCounts),
"RB" => Ok(Self::TotalRepeatSequenceBaseCounts),
"CIRUC" => Ok(Self::RepeatUnitCountConfidenceIntervals),
"CIRB" => Ok(Self::TotalRepeatSequenceBaseCountConfidenceIntervals),
"RUB" => Ok(Self::RepeatUnitBaseCounts),
_ => Err(ParseError::Invalid),
}
}
}