
501 - 1000 employees
Founded 1978
🧬 Biotechnology
🔬 Science
Biotechnology • Science
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
🧬 Biotechnology
🔬 Science
Biotechnology • Science
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.
• Review test requisition forms and clinical notes • Perform case analysis using the Emedgene platform • Identify and select variants relevant to the proband’s phenotype • Request confirmatory testing when necessary • Communicate findings at cross-team huddles • Opportunities for cross-training in WGS variant curations or clinical indication may become available as needed
• Degree: Masters in Genetic Counseling, MD, or PhD in clinical medicine, genetics, molecular biology, or equivalent • Familiarity with American College of Medical Genetics (ACMG) variant curation guidelines • 1 year of prior experience with whole exome or whole genome case review is preferred (for rank I) • 2 years of experience with whole exome or whole genome case review is preferred (for rank II) • 5 years of experience with whole exome or whole genome case review is preferred (for rank III) • 7 years of experience with whole exome or whole genome case review is preferred (for senior rank) • 10 years of experience with whole exome or whole genome case review is preferred (for professional rank) • Demonstration of thorough expertise of gene-disease correlation, case analysis variant selection
• Daily team huddles • Clear objectives • Flexible scheduling
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