CORD-19:ee0a7632371a08727d41e55aad7d621daeceef7d / 461501-461747 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/CORD-19/sourceid/ee0a7632371a08727d41e55aad7d621daeceef7d","sourcedb":"CORD-19","sourceid":"ee0a7632371a08727d41e55aad7d621daeceef7d","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.","tracks":[{"project":"CORD-19-Sentences","denotations":[{"id":"T67175","span":{"begin":0,"end":246},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"attributes":[{"subj":"T67175","pred":"source","obj":"CORD-19-Sentences"}]},{"project":"CORD-19_Custom_license_subset","denotations":[{"id":"T99","span":{"begin":0,"end":246},"obj":"Sentence"}],"attributes":[{"subj":"T99","pred":"source","obj":"CORD-19_Custom_license_subset"}]},{"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"},{"subj":"T906","pred":"source","obj":"CORD-19-PD-HP"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"CORD-19-Sentences","color":"#ece093","default":true},{"id":"CORD-19_Custom_license_subset","color":"#c693ec"},{"id":"CORD-19-PD-HP","color":"#93ecac"}]}]}}