Best practices for variant calling in clinical sequencingDaniel C. Koboldt(Nationwide Children's Hospital)Genome MedicineOctober 26, 202010.1186/s13073-020-00791-wCited by 409SaveCiteExport RISWatch citationsRelated PapersWhole-genome analysis informs breast cancer response to aromatase inhibition|Nature|2012|1kExome sequencing of Finnish isolates enhances rare-variant association power|Nature|2019|217PTEN somatic mutations contribute to spectrum of cerebral overgrowth|Brain|2021|42