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Add initial pipelne job to cleanup extraneous MHC typing results
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4 files changed

+22
-1
lines changed

4 files changed

+22
-1
lines changed

SequenceAnalysis/resources/queries/sequenceanalysis/alignment_summary_by_lineage.query.xml

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@@ -38,6 +38,10 @@
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</conditionalFormat>
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</conditionalFormats>
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</column>
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<column columnName="rowids">
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<columnTitle>RowIds</columnTitle>
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<isHidden>true</isHidden>
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</column>
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</columns>
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</table>
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</tables>

SequenceAnalysis/resources/queries/sequenceanalysis/alignment_summary_by_lineage.sql

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@@ -34,6 +34,7 @@ select
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SELECT distinct asj.alignment_id from sequenceanalysis.alignment_summary_junction asj WHERE asj.ref_nt_id.locus = a.loci and asj.status = true
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)
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) as float)), 2) as percent_from_locus,
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group_concat(distinct a.rowid, ',') as rowids
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FROM (
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SequenceAnalysis/resources/queries/sequenceanalysis/alignment_summary_grouped.query.xml

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@@ -50,6 +50,18 @@
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</conditionalFormat>
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</conditionalFormats>
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</column>
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<column columnName="rowids">
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<columnTitle>RowIds</columnTitle>
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<isHidden>true</isHidden>
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</column>
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<column columnName="nAlignments">
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<columnTitle># Alignments</columnTitle>
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<isHidden>true</isHidden>
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</column>
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<column columnName="nLoci">
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<columnTitle># Loci</columnTitle>
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<isHidden>true</isHidden>
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</column>
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</columns>
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</table>
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</tables>

SequenceAnalysis/resources/queries/sequenceanalysis/alignment_summary_grouped.sql

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@@ -45,7 +45,10 @@ select
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SELECT distinct asj.alignment_id from sequenceanalysis.alignment_summary_junction asj WHERE asj.ref_nt_id.locus = a.loci and asj.status = true
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)
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) as float) END), 2) as percent_from_locus,
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max(lastModified) as lastModified
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max(lastModified) as lastModified,
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group_concat(distinct a.rowid, ',') as rowids,
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count(distinct a.rowid) as nAlignments,
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max(a.nloci) as nLoci
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FROM (
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@@ -58,6 +61,7 @@ FROM (
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group_concat(distinct j.ref_nt_id.lineage, chr(10)) as lineages,
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count(distinct j.ref_nt_id.lineage) as totalLineages,
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group_concat(distinct j.ref_nt_id.locus, chr(10)) as loci,
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count(distinct j.ref_nt_id.locus) as nloci,
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group_concat(distinct hs.haplotype, chr(10)) as haplotypesWithAllele,
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total,

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