{"id":"W2139747296","doi":"10.1038/ng.437","title":"Personalized copy number and segmental duplication maps using next-generation sequencing","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":776,"is_retracted":false,"has_abstract":false,"ca_institutions":"Simon Fraser University","funders":"National Human Genome Research Institute; Howard Hughes Medical Institute; National Science Foundation","keywords":"Copy-number variation; Segmental duplication; Biology; Gene duplication; Genome; Structural variation; Sequence (biology); Gene; Genetics; Human genome; Copy number analysis; Computational biology; Constraint (computer-aided design); DNA sequencing; Gene dosage; Gene family; Mathematics","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":0.02391843337455049,"score_gpt":0.2650377693914083,"score_spread":0.2411193360168578,"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."}}