mirror of
https://github.com/MillironX/SequenceVariation.jl.git
synced 2024-11-29 07:59:55 +00:00
288 lines
8.9 KiB
Julia
288 lines
8.9 KiB
Julia
"""
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Needs to be able to:
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* Given a sequence and a reference, create a `Haplotype` that unambiguously represents
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the sequence
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* Given a `Haplotype` and a new reference, translate the variant to the new reference.
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* Given a mutation and a reference and a sequence, determine if the sequence has that
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mutation
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TODO now:
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* Create a string repr and parser for Edit, perhaps
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* A243T for sub
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* 119TAGGCTA for insertion
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* TGAGCTA9 for deletion
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* Create a parser + print/show for edit
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* Play around with some NGS results rel. to picked reference.
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* Is it easy to construct ref and variants? I.e. is API nice?
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* Is it nice and easy to check if a mut is present?
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*
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* Implement "reference switching".
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* Add tests
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"""
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using Aqua
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using BioAlignments:
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AffineGapScoreModel,
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GlobalAlignment,
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EDNAFULL,
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pairalign,
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Alignment,
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AlignedSequence,
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PairwiseAlignment
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using BioSequences: BioSequence, @dna_str, ungap!
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using BioSymbols: DNA_A
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using SequenceVariation
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using Test
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const DNA_MODEL = AffineGapScoreModel(EDNAFULL; gap_open=-25, gap_extend=-2)
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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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seq3 = ungap!(dna"-GATGCGTGT-AGCAACACTTATCGC-")
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var = Haplotype(align(seq1, seq2))
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const SEQ = typeof(seq1)
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const BSE = eltype(seq1)
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@testset "EditSorting" begin
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S = typeof(seq1)
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T = eltype(seq1)
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@test SequenceVariation.Edit{S,T}(Deletion(1), 1) <
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SequenceVariation.Edit{S,T}(Deletion(1), 2)
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@test SequenceVariation.Edit{S,T}(Deletion(1), 1) <
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SequenceVariation.Edit{S,T}(Deletion(2), 1)
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end
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@testset "HaplotypeValidation" begin
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# Test that we can't use an empty reference
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@test_throws ErrorException Haplotype(
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dna"", [SequenceVariation.Edit{SEQ,BSE}(Insertion{SEQ}(dna"A"), 0)]
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)
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# Test that substitutions cannot share the same position
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@test_throws ErrorException Haplotype(
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seq2, [Variation(seq2, "T2A"), Variation(seq2, "T2C")]
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)
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@test_throws ErrorException Haplotype(
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seq2, [Variation(seq2, "G2A"), Variation(seq2, "G2T")]
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)
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@test_throws ErrorException Haplotype(
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seq2, [Variation(seq2, "G26A"), Variation(seq2, "G26T")]
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)
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# Test that insertions cannot share the same position
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@test_throws ErrorException Haplotype(
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seq2, [Variation(seq2, "0AAA"), Variation(seq2, "0TTT")]
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)
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@test_throws ErrorException Haplotype(
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seq2, [Variation(seq2, "2AAA"), Variation(seq2, "2TTT")]
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)
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@test_throws ErrorException Haplotype(
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seq2, [Variation(seq2, "26AAA"), Variation(seq2, "26TTT")]
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)
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# Test that deletions invalidate further operations within the deleted positions
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@test_throws ErrorException Haplotype(
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seq2, [Variation(seq2, "Δ2-2"), Variation(seq2, "G2A")]
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)
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@test_throws ErrorException Haplotype(
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seq2, [Variation(seq2, "G2A"), Variation(seq2, "Δ2-2")]
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)
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@test_throws ErrorException Haplotype(
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seq2, [Variation(seq2, "Δ2-6"), Variation(seq2, "Δ3-5")]
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)
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# Test that a complicated (but valid) Haplotype still checks out
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@test first(
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SequenceVariation._is_valid(
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Haplotype(
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seq2,
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[
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Variation(seq2, "0AAA"),
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Variation(seq2, "T2A"),
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Variation(seq2, "Δ5-8"),
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Variation(seq2, "G26A"),
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],
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),
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),
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)
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end
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@testset "HaplotypeRoundtrip" begin
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for v in variations(var)
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@test v in var
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@test v in Haplotype(seq2, [v])
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end
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end
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@testset "HaplotypeReconstruction" begin
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@test reconstruct(var) == seq1
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end
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@testset "VariationSorting" begin
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@test Variation(seq2, "A3T") < Variation(seq2, "T4A")
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end
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@testset "HaplotypeTranslation" begin
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ref1 = seq2
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ref2 = seq3
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alt = seq1
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@test all(
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v -> v in Haplotype(align(alt, ref2)), variations(translate(var, align(ref2, ref1)))
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)
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end
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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 Haplotype(aln01).edits == Haplotype(aln02).edits
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end
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@testset "VariationParsing" begin
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refseq = dna"ACAACTTTATCT"
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sub = Variation(refseq, "A4T")
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del = Variation(refseq, "Δ4-5")
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ins = Variation(refseq, "4TT")
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@test mutation(sub) isa Substitution
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@test mutation(del) isa Deletion
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@test mutation(ins) isa Insertion
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end
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@testset "VariationRetrieval" begin
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refseq = dna"ACAACTTTATCT"
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mutseq = dna"ACATCTTTATCT"
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read = AlignedSequence(mutseq[1:10], Alignment("10M", 1, 1))
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aln = PairwiseAlignment(read, refseq)
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var = Haplotype(aln)
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sub = Variation(refseq, "A4T")
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@test first(variations(var)) == sub
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end
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@testset "VariationTranslation" begin
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ref1 = seq2
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ref2 = seq3
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ref3 = copy(ref1)
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ref3[1] = DNA_A
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alt = seq1
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ref2_on_ref1 = align(ref2, ref1)
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alt_on_ref1 = align(alt, ref1)
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ref1_on_alt = align(ref1, alt)
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ref3_on_ref1 = align(ref3, ref1)
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# Test insertion at position zero
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@test translate(Variation(ref1, "0CAT"), ref2_on_ref1) ==
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SequenceVariation.Inapplicable()
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@test translate(Variation(ref1, "0CAT"), ref3_on_ref1) == Variation(ref3, "0CAT")
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# Test substitution on deletion
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@test isnothing(translate(Variation(ref1, "A17T"), ref1_on_alt))
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# Test substitution to itself
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@test isnothing(translate(Variation(ref1, "A23C"), ref2_on_ref1))
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# Test simple substitution
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@test translate(Variation(ref1, "T10A"), ref2_on_ref1) == Variation(ref2, "T9A")
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# Test simple deletion
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@test translate(Variation(ref1, "Δ17-18"), ref2_on_ref1) == Variation(ref2, "Δ16-17")
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# Test deletion on deletion
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@test isnothing(translate(Variation(ref1, "Δ17-17"), alt_on_ref1))
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# Test simple insertion
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@test translate(Variation(ref1, "6CAT"), ref2_on_ref1) == Variation(ref2, "5CAT")
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# Test two insertions at the same position
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@test translate(Variation(ref1, "10G"), alt_on_ref1) == SequenceVariation.Inapplicable()
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# Test insertion on deletion
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@test translate(Variation(ref1, "17CAT"), alt_on_ref1) ==
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SequenceVariation.Inapplicable()
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end
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@testset "VariationBases" begin
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# Test substition bases
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@test refbases(Variation(dna"ATCGA", "C3G")) == dna"C"
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@test altbases(Variation(dna"ATCGA", "C3G")) == dna"G"
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# Test single deletion bases
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@test refbases(Variation(dna"ATCGA", "Δ3-3")) == dna"TC"
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@test altbases(Variation(dna"ATCGA", "Δ3-3")) == dna"T"
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# Test multiple deletion bases
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@test refbases(Variation(dna"ATCGA", "Δ3-4")) == dna"TCG"
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@test altbases(Variation(dna"ATCGA", "Δ3-4")) == dna"T"
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# Test first position deletion
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@test refbases(Variation(dna"ATCGA", "Δ1-1")) == dna"AT"
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@test altbases(Variation(dna"ATCGA", "Δ1-1")) == dna"T"
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# Test single insertion bases
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@test refbases(Variation(dna"ATCGA", "3A")) == dna"C"
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@test altbases(Variation(dna"ATCGA", "3A")) == dna"CA"
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# Test multiple insertion bases
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@test refbases(Variation(dna"ATCGA", "3TAG")) == dna"C"
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@test altbases(Variation(dna"ATCGA", "3TAG")) == dna"CTAG"
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# Test first position insertion
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@test refbases(Variation(dna"ATCGA", "1C")) == dna"A"
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@test altbases(Variation(dna"ATCGA", "1C")) == dna"CA"
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end
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@testset "SoftclipHaplotype" begin
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refseq = dna"GATTACA"
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mutseq = dna"GATTACAAAA"
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refvar = Haplotype(refseq, SequenceVariation.Edit{typeof(refseq),eltype(refseq)}[])
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# Test for ending soft clip
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@test Haplotype(
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PairwiseAlignment(AlignedSequence(mutseq, Alignment("7=3S", 1, 1)), refseq)
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) == refvar
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# Test for ending soft+hard clip
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@test Haplotype(
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PairwiseAlignment(AlignedSequence(mutseq, Alignment("7=3S2H", 1, 1)), refseq)
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) == refvar
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# Test that ending insertions are still valid
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@test length(
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Haplotype(
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PairwiseAlignment(AlignedSequence(mutseq, Alignment("7=3I", 1, 1)), refseq)
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).edits,
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) == 1
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# Test that out-of-bounds bases are still caught
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@test_throws BoundsError Haplotype(
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PairwiseAlignment(AlignedSequence(mutseq, Alignment("7=3X", 1, 1)), refseq)
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)
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end
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@testset "Aqua" begin
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Aqua.test_ambiguities(SequenceVariation; recursive=false)
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# TODO: Refactor `Edit` so that this test doesn't fail
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# TODO: This test _should_ be set to @test_fails, but Aqua's syntax doesn't allow that
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# Aqua.test_unbound_args(SequenceVariation)
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Aqua.test_undefined_exports(SequenceVariation)
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Aqua.test_piracy(SequenceVariation)
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Aqua.test_project_extras(SequenceVariation)
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Aqua.test_stale_deps(SequenceVariation)
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Aqua.test_deps_compat(SequenceVariation)
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Aqua.test_project_toml_formatting(SequenceVariation)
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end
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