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    <!-- 
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000117"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000119"/>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000116"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000412"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000112"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000111"/>
    


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    <!-- http://purl.obolibrary.org/obo/IAO_0000078 -->

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    <!-- http://purl.obolibrary.org/obo/OBI_0000626 -->

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        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">DNA sequencing assay</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/OBI_0002117 -->

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        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">whole genome sequencing assay</rdfs:label>
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        <ns2:IAO_0000115 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">A DNA sequencing assay that intends to provide information about the sequence of an entire genome of an organism.</ns2:IAO_0000115>
        <ns2:IAO_0000116 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Genotyping assays should ideally identify which part of the genome the information is about. We do not currently have a good way to do this. That information should be added later.</ns2:IAO_0000116>
        <ns2:IAO_0000117 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">ImmPort</ns2:IAO_0000117>
        <ns2:IAO_0000119 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">PMID:23095910</ns2:IAO_0000119>
        <ns2:IAO_0000119 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">PMID:25827230</ns2:IAO_0000119>
        <ns2:IAO_0000118 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">WGS</ns2:IAO_0000118>
        <ns2:IAO_0000112 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">WGS permits comprehensive sequencing of introns and exons, whereas whole exome sequencing (WES) allows deeper sequencing of exonic regions at a lower cost. Due to the large number of genetic variants found in each genome, it is necessary to use filtering approaches to distinguish deleterious from benign variants. WES has been used successfully to identify novel genetic causes of primary immunodeficiency. Complex structural variations and non-Mendelian disorders remain challenges for WGS.</ns2:IAO_0000112>
        <ns2:IAO_0000111 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">whole genome sequencing assay</ns2:IAO_0000111>
        <ns2:IAO_0000114 rdf:resource="http://purl.obolibrary.org/obo/IAO_0000120"/>
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        <rdfs:label xml:lang="en">metadata complete</rdfs:label>
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