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Update API documentation for different translate
methods
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2 changed files with 6 additions and 3 deletions
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@ -22,6 +22,7 @@ Haplotype
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reference(::Haplotype)
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reference(::Haplotype)
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variations
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variations
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reconstruct
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reconstruct
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translate(::Haplotype{S,T}, ::PairwiseAlignment{S,S}) where {S,T}
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```
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```
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## Variations
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## Variations
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@ -30,7 +31,7 @@ reconstruct
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Variation
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Variation
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reference(::Variation)
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reference(::Variation)
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mutation
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mutation
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translate
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translate(::Variation{S,T}, ::PairwiseAlignment{S,S}) where {S,T}
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refbases
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refbases
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altbases
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altbases
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```
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```
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@ -54,13 +54,15 @@ variations(bos_human_haplotype)
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## Reference switching
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## Reference switching
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An individual variation can be mapped to a new reference sequence given an
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An individual variation can be mapped to a new reference sequence given an
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alignment between the new and old references using the [`translate`](@ref).
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alignment between the new and old references using the
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[`translate`](@ref translate(::Variation{S,T}, ::PairwiseAlignment{S,S}) where {S,T})
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function.
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```@repl call_variants
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```@repl call_variants
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ovis_human_alignment =
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ovis_human_alignment =
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PairwiseAlignment(AlignedSequence(human, Alignment("32M", 1, 1)), ovine)
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PairwiseAlignment(AlignedSequence(human, Alignment("32M", 1, 1)), ovine)
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human_variation = first(variations(bos_ovis_haplotype))
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human_variation = first(variations(bos_ovis_haplotype))
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reference(ans) == bovine
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reference(ans) == bovine
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SequenceVariation.translate(human_variation, ovis_human_haplotype)
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SequenceVariation.translate(human_variation, ovis_human_alignment)
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reference(ans) == bovine
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reference(ans) == bovine
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```
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```
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