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    <!-- 
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    //
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    <!-- http://purl.obolibrary.org/obo/PCL_0010002 -->

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    <!-- http://schema.org/Dataset -->

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    <!-- http://purl.obolibrary.org/obo/PCL_0016454 -->

    <NamedIndividual rdf:about="http://purl.obolibrary.org/obo/PCL_0016454">
        <rdf:type rdf:resource="http://schema.org/Dataset"/>
        <rdfs:label>Human M1 (CCN201912131) single nuclei SNARE-seq2</rdfs:label>
        <ns2:PCL_0010061 rdf:datatype="http://www.w3.org/2001/XMLSchema#integer">84178</ns2:PCL_0010061>
        <ns2:IAO_0000028>Human M1 SNARE-seq2</ns2:IAO_0000028>
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        <ns3:discussionUrl>https://nemoanalytics.org//index.html?layout_id=ac9863bf</ns3:discussionUrl>
        <skos:prefLabel>SNARE-seq2</skos:prefLabel>
        <rdfs:comment>A sequencing assay that involves the isolation of single nuclei and open chromatin tagmentation in the isolated nuclei using a transposase. The tagmented nuclei are then encapsulated in a droplet including both an oligo-dT-containing barcoded bead and a splint oligonucleotide, which links the tagmented gDNA fragments to the bead, enabling the bead to capture both mRNAs and open chromatin fragments. After mRNAs and gDNA fragments are released from the bead by heating, RT and PCR amplification are performed to generate a library of cDNA and open chromatin gDNA fragments.
</rdfs:comment>
        <ns3:position>M1</ns3:position>
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