CORD-19:ee0a7632371a08727d41e55aad7d621daeceef7d / 461501-461747 JSONTXT

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    CORD-19-Sentences

    {"project":"CORD-19-Sentences","denotations":[{"id":"T67175","span":{"begin":0,"end":246},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Shallow whole genome sequencing, where average read-depth can be as low as 0.1x, provides a cost savings-approach for identification of large copy number variant (CNV) events; it has been utilized in various application areas, including oncology."}

    CORD-19_Custom_license_subset

    {"project":"CORD-19_Custom_license_subset","denotations":[{"id":"T99","span":{"begin":0,"end":246},"obj":"Sentence"}],"text":"Shallow whole genome sequencing, where average read-depth can be as low as 0.1x, provides a cost savings-approach for identification of large copy number variant (CNV) events; it has been utilized in various application areas, including oncology."}

    CORD-19-PD-HP

    {"project":"CORD-19-PD-HP","denotations":[{"id":"T906","span":{"begin":237,"end":245},"obj":"Phenotype"}],"attributes":[{"id":"A906","pred":"hp_id","subj":"T906","obj":"http://purl.obolibrary.org/obo/HP_0002664"}],"text":"Shallow whole genome sequencing, where average read-depth can be as low as 0.1x, provides a cost savings-approach for identification of large copy number variant (CNV) events; it has been utilized in various application areas, including oncology."}