Add tests for `translate(::Variation)`

master
parent f38f0edb00
commit 239b366a1c

@ -24,16 +24,25 @@ TODO now:
"""
using Aqua
using BioAlignments
using BioSequences
using BioAlignments:
AffineGapScoreModel,
GlobalAlignment,
EDNAFULL,
pairalign,
Alignment,
AlignedSequence,
PairwiseAlignment
using BioSequences: BioSequence, @dna_str, ungap!
using BioSymbols: DNA_A
using SequenceVariation
using Test
const DNA_MODEL = BioAlignments.AffineGapScoreModel(EDNAFULL; gap_open=-25, gap_extend=-2)
const DNA_MODEL = AffineGapScoreModel(EDNAFULL; gap_open=-25, gap_extend=-2)
align(a::BioSequence, b::BioSequence) = pairalign(GlobalAlignment(), a, b, DNA_MODEL).aln
seq1 = ungap!(dna"--ATGCGTGTTAGCAAC--TTATCGCG")
seq2 = ungap!(dna"TGATGCGTGT-AGCAACACTTATAGCG")
seq3 = ungap!(dna"-GATGCGTGT-AGCAACACTTATCGC-")
var = Haplotype(align(seq1, seq2))
@testset "EditSorting" begin
@ -95,6 +104,49 @@ end
@test first(variations(var)) == sub
end
@testset "VariationTranslation" begin
ref1 = seq2
ref2 = seq3
ref3 = copy(ref1)
ref3[1] = DNA_A
alt = seq1
ref2_on_ref1 = align(ref2, ref1)
alt_on_ref1 = align(alt, ref1)
ref1_on_alt = align(ref1, alt)
ref3_on_ref1 = align(ref3, ref1)
# Test insertion at position zero
@test translate(Variation(ref1, "0CAT"), ref2_on_ref1) ==
SequenceVariation.Inapplicable()
@test translate(Variation(ref1, "0CAT"), ref3_on_ref1) == Variation(ref3, "0CAT")
# Test substitution on deletion
@test isnothing(translate(Variation(ref1, "A17T"), ref1_on_alt))
# Test substitution to itself
@test isnothing(translate(Variation(ref1, "A23C"), ref2_on_ref1))
# Test simple substitution
@test translate(Variation(ref1, "T10A"), ref2_on_ref1) == Variation(ref2, "T9A")
# Test simple deletion
@test translate(Variation(ref1, "Δ17-18"), ref2_on_ref1) == Variation(ref2, "Δ16-17")
# Test deletion on deletion
@test isnothing(translate(Variation(ref1, "Δ17-17"), alt_on_ref1))
# Test simple insertion
@test translate(Variation(ref1, "6CAT"), ref2_on_ref1) == Variation(ref2, "5CAT")
# Test two insertions at the same position
@test translate(Variation(ref1, "10G"), alt_on_ref1) == SequenceVariation.Inapplicable()
# Test insertion on deletion
@test translate(Variation(ref1, "17CAT"), alt_on_ref1) ==
SequenceVariation.Inapplicable()
end
@testset "VariationBases" begin
# Test substition bases
@test refbases(Variation(dna"ATCGA", "C3G")) == dna"C"

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