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fnothaftheuermh
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Line wrap SupportedHeaderLines to break long lines.
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adam-core/src/main/scala/org/bdgenomics/adam/converters/SupportedHeaderLines.scala

Lines changed: 56 additions & 14 deletions
Original file line numberDiff line numberDiff line change
@@ -28,20 +28,62 @@ import htsjdk.variant.vcf.{
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*/
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private[adam] object SupportedHeaderLines {
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lazy val ancestralAllele = new VCFInfoHeaderLine("AA", 1, VCFHeaderLineType.String, "Ancestral allele");
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lazy val alleleCount = new VCFInfoHeaderLine("AC", VCFHeaderLineCount.A, VCFHeaderLineType.Integer, "Allele count");
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lazy val readDepth = new VCFInfoHeaderLine("AD", VCFHeaderLineCount.R, VCFHeaderLineType.Integer, "Total read depths for each allele");
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lazy val forwardReadDepth = new VCFInfoHeaderLine("ADF", VCFHeaderLineCount.R, VCFHeaderLineType.Integer, "Read depths for each allele on the forward strand");
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lazy val reverseReadDepth = new VCFInfoHeaderLine("ADR", VCFHeaderLineCount.R, VCFHeaderLineType.Integer, "Read depths for each allele on the reverse strand");
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lazy val alleleFrequency = new VCFInfoHeaderLine("AF", VCFHeaderLineCount.A, VCFHeaderLineType.Float, "Allele frequency for each allele");
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lazy val cigar = new VCFInfoHeaderLine("CIGAR", VCFHeaderLineCount.A, VCFHeaderLineType.String, "Cigar string describing how to align alternate alleles to the reference allele");
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lazy val dbSnp = new VCFInfoHeaderLine("DB", 0, VCFHeaderLineType.Flag, "Membership in dbSNP");
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lazy val hapMap2 = new VCFInfoHeaderLine("H2", 0, VCFHeaderLineType.Flag, "Membership in HapMap2");
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lazy val hapMap3 = new VCFInfoHeaderLine("H3", 0, VCFHeaderLineType.Flag, "Membership in HapMap3");
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lazy val validated = new VCFInfoHeaderLine("VALIDATED", 0, VCFHeaderLineType.Flag, "Validated by follow-up experiment");
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lazy val thousandGenomes = new VCFInfoHeaderLine("1000G", 0, VCFHeaderLineType.Flag, "Membership in 1000 Genomes");
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lazy val somatic = new VCFInfoHeaderLine("SOMATIC", 0, VCFHeaderLineType.Flag, "Somatic event");
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lazy val transcriptEffects = new VCFInfoHeaderLine("ANN", VCFHeaderLineCount.UNBOUNDED, VCFHeaderLineType.String, "Functional annotations: 'Allele | Annotation | Annotation_Impact | Gene_Name | Gene_ID | Feature_Type | Feature_ID | Transcript_BioType | Rank | HGVS.c | HGVS.p | cDNA.pos / cDNA.length | CDS.pos / CDS.length | AA.pos / AA.length | Distance | ERRORS / WARNINGS / INFO'");
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lazy val ancestralAllele = new VCFInfoHeaderLine("AA",
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1,
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VCFHeaderLineType.String,
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"Ancestral allele");
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lazy val alleleCount = new VCFInfoHeaderLine("AC",
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VCFHeaderLineCount.A,
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VCFHeaderLineType.Integer,
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"Allele count");
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lazy val readDepth = new VCFInfoHeaderLine("AD",
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VCFHeaderLineCount.R,
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VCFHeaderLineType.Integer,
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"Total read depths for each allele");
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lazy val forwardReadDepth = new VCFInfoHeaderLine("ADF",
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VCFHeaderLineCount.R,
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VCFHeaderLineType.Integer,
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"Read depths for each allele on the forward strand");
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lazy val reverseReadDepth = new VCFInfoHeaderLine("ADR",
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VCFHeaderLineCount.R,
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VCFHeaderLineType.Integer,
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"Read depths for each allele on the reverse strand");
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lazy val alleleFrequency = new VCFInfoHeaderLine("AF",
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VCFHeaderLineCount.A,
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VCFHeaderLineType.Float,
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"Allele frequency for each allele");
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lazy val cigar = new VCFInfoHeaderLine("CIGAR",
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VCFHeaderLineCount.A,
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VCFHeaderLineType.String,
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"Cigar string describing how to align alternate alleles to the reference allele");
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lazy val dbSnp = new VCFInfoHeaderLine("DB",
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0,
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VCFHeaderLineType.Flag,
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"Membership in dbSNP");
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lazy val hapMap2 = new VCFInfoHeaderLine("H2",
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0,
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VCFHeaderLineType.Flag,
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"Membership in HapMap2");
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lazy val hapMap3 = new VCFInfoHeaderLine("H3",
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0,
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VCFHeaderLineType.Flag,
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"Membership in HapMap3");
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lazy val validated = new VCFInfoHeaderLine("VALIDATED",
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0,
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VCFHeaderLineType.Flag,
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"Validated by follow-up experiment");
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lazy val thousandGenomes = new VCFInfoHeaderLine("1000G",
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0,
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VCFHeaderLineType.Flag,
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"Membership in 1000 Genomes");
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lazy val somatic = new VCFInfoHeaderLine("SOMATIC",
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0,
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VCFHeaderLineType.Flag,
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"Somatic event");
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lazy val transcriptEffects = new VCFInfoHeaderLine("ANN",
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VCFHeaderLineCount.UNBOUNDED,
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VCFHeaderLineType.String,
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"Functional annotations: 'Allele | Annotation | Annotation_Impact | Gene_Name | Gene_ID | Feature_Type | Feature_ID | Transcript_BioType | Rank | HGVS.c | HGVS.p | cDNA.pos / cDNA.length | CDS.pos / CDS.length | AA.pos / AA.length | Distance | ERRORS / WARNINGS / INFO'");
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/**
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* All info keys in VCF format.

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