{"id":"W2116126626","doi":"10.1038/nature09708","title":"Mapping copy number variation by population-scale genome sequencing","year":2011,"lang":"en","type":"article","venue":"Nature","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1210,"is_retracted":false,"has_abstract":false,"ca_institutions":"Simon Fraser University","funders":"National Human Genome Research Institute; National Institute of General Medical Sciences; National Institute of Mental Health; National Institute on Alcohol Abuse and Alcoholism; National Institute for Health and Care Research; Wellcome Trust","keywords":"Copy-number variation; Biology; Genome; Variation (astronomy); Scale (ratio); Population; Evolutionary biology; Structural variation; Computational biology; Genetics; Geography; Gene; Demography; Cartography; Astronomy","routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false,"invisible_to_affiliation_only":false},"retraction":null,"screen":null,"machine_scores":{"provisional":true,"baseline":true,"maturity_gate_passed":false,"score_opus":0.008005499921224407,"score_gpt":0.2116816712362102,"score_spread":0.2036761713149858,"validation_status":"score_only:v0-immature-baseline","note":"Baseline scores from an immature model (maturity gate not passed). Scores rank; they never assert a category."}}