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Fix inconsistent Variation positions (#4)
* Change Variant constructor to use alignment positions Signed-off-by: Thomas A. Christensen II <25492070+MillironX@users.noreply.github.com> * Add test for positions of Variations Signed-off-by: Thomas A. Christensen II <25492070+MillironX@users.noreply.github.com>
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2 changed files with 14 additions and 2 deletions
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@ -242,7 +242,8 @@ function Variant(aln::PairwiseAlignment{T, T}) where {T <: LongSequence{<:Union{
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E = eltype(typeof(ref))
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edits = Edit{T, E}[]
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result = Variant(ref, edits)
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refpos = seqpos = 0
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refpos = first(aln.a.aln.anchors).refpos
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seqpos = first(aln.a.aln.anchors).seqpos
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markpos = 0
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n_gaps = n_ins = 0
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insertion_buffer = E[]
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@ -32,4 +32,15 @@ const DNA_MODEL = BioAlignments.AffineGapScoreModel(EDNAFULL, gap_open=-25, gap_
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align(a::BioSequence, b::BioSequence) = pairalign(GlobalAlignment(), a, b, DNA_MODEL).aln
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seq1 = ungap!(dna"--ATGCGTGTTAGCAAC--TTATCGCG")
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seq2 = ungap!(dna"TGATGCGTGT-AGCAACACTTATAGCG")
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var = Variant(align(seq1, seq2))
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var = Variant(align(seq1, seq2))
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@testset "VariationPosition" begin
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refseq = dna"ACAACTTTATCT"
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mutseq = dna"ACATCTTTATCT"
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read01 = AlignedSequence(mutseq[1:10], Alignment("10M", 1, 1))
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read02 = AlignedSequence(mutseq[3:12], Alignment("10M", 1, 3))
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aln01 = PairwiseAlignment(read01, refseq)
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aln02 = PairwiseAlignment(read02, refseq)
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@test Variant(aln01).edits == Variant(aln02).edits
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end
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