For nearly 40 years, Baylor Genetics has been the leading pioneer in genetic testing. Currently, we offer a full spectrum of cost-effective, genetic testing and provide clinically relevant solutions. Our team’s unmatched knowledge and experience deliver a combination of advanced technology and deep patient data sets that lead to more accurate interpretations.
Baylor Genetics pioneered the history of genetic testing. Now, we’re leading the way in precision medicine.
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ONE MISSION
Improve Care Through Genetics
If your question can be answered through genetic testing, we have the test you need.
With nearly 4,000 test options, no specialty genetics provider offers a selection broader than ours. Baylor genetics delivers the tests and leading accuracy you insist on. Backed by nearly four decades of research and development, we have the appropriate tests for your patient.
Laboratory Capabilities
Whole Exome Sequencing
Point mutations, insertions, deletions, inversion and rearrangements of the exome are potentially discoverable.
Prenatal Diagnostics
Carrier testing, prenatal exome.
Cytogenetics
Chromosomal analysis, plus FISH analysis for over 25 genetic disorders and active in the area of cancer cytogenetics.
Molecular Diagnostics
DNA-based testing for the molecular diagnosis, carrier and prenatal testing of hereditary disorders, testing over 150 genes, including rare genes.
Oncology
Cancer mutation panels using NGS, cancer microarrays, single gene sequencing, FISH analysis, chromosome analysis ,deletion/duplication analysis.
Chromosomal Microarray Analysis
Exon coverage, whole genome coverage, SNP analysis, mitochondrial genome coverage, microRNAs and more.
Biochemical
Featuring our exclusive Global MAPS test for errors of inborn metabolism, plus broad spectrum of quantitative analyses – over 30 enzyme assays.
Interpretation Services
Baylor Genetics offers interpretation services allowing rapid access to genetic experts, deep patient data sets and cutting-edge bioinformatics technology delivering results your patients can trust.
Laboratory Capabilities
Whole Exome Sequencing
Point mutations, insertions, deletions, inversion and rearrangements of the exome are potentially discoverable.
Molecular Diagnostics
DNA-based testing for the molecular diagnosis, carrier and prenatal testing of hereditary disorders, testing over 150 genes, including rare genes.
Oncology
Cancer mutation panels using NGS, cancer microarrays, single gene sequencing, FISH analysis, chromosome analysis ,deletion/duplication analysis.
Interpretation Services
Baylor Genetics offers interpretation services allowing rapid access to genetic experts, deep patient data sets and cutting-edge bioinformatics technology delivering results your patients can trust.
Prenatal Diagnostics
Carrier testing, prenatal exome.
Cytogenetics
Chromosomal analysis, plus FISH analysis for over 25 genetic disorders and active in the area of cancer cytogenetics.
Chromosomal Microarray Analysis
Exon coverage, whole genome coverage, SNP analysis, mitochondrial genome coverage, microRNAs and more.
Biochemical
Featuring our exclusive Global MAPS test for errors of inborn metabolism, plus broad spectrum of quantitative analyses – over 30 enzyme assays.
Genetic testing is not just the core of our business, it’s in our DNA.
The Baylor Genetics team consists of PhDs and genetic counselors who have been featured in prominent journals, such as JAMA, Science, and Nature. In addition to our team, Baylor Genetics is complemented with the staff, medical geneticists, faculty, genetic counselors, and researchers at Baylor College of Medicine. Through these combined efforts, we are able to drive new discoveries in research and testing.
