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Inherited and de novo variants extend the etiology of TAOK1-associated neurodevelopmental disorder
Genetic changes associated with relapse in favorable histology Wilms tumor: A Children’s Oncology Group AREN03B2 study
Evaluation of three microhaplotypes in individual identification and ancestry inference
Applicability of ancestral genotyping in pharmacogenomic research with hormonal contraception
Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients
Far from home: A multi-analytical approach revealing the journey of an African-born individual to imperial Rome
Human sample authentication in biomedical research: comparison of two platforms
Ancestry analysis using autosomal SNPs in northern South America, reveals interpretation differences between an AIM panel and an identification panel
Characterization of a castrate-resistant prostate cancer xenograft derived from a patient of West African ancestry
Somatic Variation as an Incidental Finding in the Pediatric Next Generation Sequencing Era