
501 - 1000 employees
Founded 1978
🏥 Healthcare
💼 Consulting
🍽️ Food & Beverage
Healthcare • Consulting • Food & Beverage
Baylor Genetics is a clinical genomics and precision diagnostics laboratory affiliated with Baylor College of Medicine that provides comprehensive genetic testing and interpretation services. The company offers whole genome and whole exome sequencing, chromosomal microarray analysis, mitochondrial testing, pharmacogenomics, and specialized assays, along with genetic counseling, provider support, and insurance/payment resources. Baylor Genetics supports healthcare providers, researchers, and families with AI-enhanced interpretation, multimodal data integration, and end-to-end clinical and laboratory services.
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501 - 1000 employees
Founded 1978
🏥 Healthcare
💼 Consulting
🍽️ Food & Beverage
Healthcare • Consulting • Food & Beverage
Baylor Genetics is a clinical genomics and precision diagnostics laboratory affiliated with Baylor College of Medicine that provides comprehensive genetic testing and interpretation services. The company offers whole genome and whole exome sequencing, chromosomal microarray analysis, mitochondrial testing, pharmacogenomics, and specialized assays, along with genetic counseling, provider support, and insurance/payment resources. Baylor Genetics supports healthcare providers, researchers, and families with AI-enhanced interpretation, multimodal data integration, and end-to-end clinical and laboratory services.
• Curation of variants, genes, and gene-disease correlations following ACMG guidelines • Analyzing clinical genomics data, including next-generation sequencing, Sanger sequencing, metabolomics, and chromosomal microarray • Clinical report drafting • Validation, process refinement, presenting findings at meetings, and performing other duties as needed
• PhD or MD level degree in clinical medicine, genetics, molecular biology, or an equivalent subject • Relevant experience: 4-7 years • Certification (optional): MB(ASCP) • Knowledge of genomic variation and its relationship to human disease • Knowledge of literature curation methodologies • Knowledge of variant detection, molecular mechanisms of disease, functional assays, and computational analysis • Technical expertise in clinical medicine, genetics, genomics, or molecular biology • Experience with data quality assessment • Proficiency in communicating an understanding of genetics details • Experience in the application of ontologies for medical/biological annotation • An understanding of bioinformatics analysis to identify variants within genomic data sets, and variant effect prediction algorithms (desired) • Experience with use of Perl, Python, or other programming language (desired) • Ability to create scripts and process large quantities of data (desired)
• Health insurance • Retirement plans • Paid time off • Flexible work arrangements • Professional development
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