Comprehensive Testing Solutions

Disease-specific TEST MENU

NOONAN SYNDROME
FRAGILE X SYNDROME
LI-FRAUMENI SYNDROME
NEUROFIBROMATOSIS
SPINAL MUSCULAR ATROPHY

SNM1 and SNM2 Deletion/Duplication

MISCELLANEOUS
CANCER GERMLINE NGS PANELS (64 GENES)

 

Colorectal Cancer Germline NGS Panel
19 Genes: 
MLH1, MSH2, MSH6, MUTYH, PMS2, EPCAM, APC, TP53, PTEN, STK11, SMAD4, BMPR1A, CDH1, CHEK2, GREM1, POLD1, POLE, ATM, AXIN2

Hereditary Breast and Ovarian Cancer Comprehensive Germline NGS Panel
21 Genes:
ATM, BARD1, BRAC1, BRAC2, BRIP1, CDH1, STK11, CHEK2, EPCAM, MLH1, MSH2, MSH6, NBN, PALB2, PMS2, PTEN, RAD51C, RAD51D, TP53, FANCC, XRCC2

Hereditary Breast and Ovarian Cancer High-Moderate Risk Germline NGS Panel
9 Genes:
ATM, BRAC1, BRAC2, BRIP1, CDH1, CHEK2, PALB2, PTEN, TP53

GET STARTED

Order a test today.

MEET DR. TAYEH

EXPERTISE DELIVERED PERSONALLY

Our quality commitment extends to how we communicate the results of our analyses. Our reports are developed with the right language and terminology to clarify complex data. I am available to answer questions and help providers prepare to discuss findings with patients and families. When more help is needed, clients can also connect with an MLabs board-certified genetic counselor.

Marwan Tayeh, Ph.D.
Associate Professor of Pediatric Genetics.
Director, Molecular Genetics 

Marwan

PERSONALIZED TESTING

YOUR FIRST STEP TO CANCER DIAGNOSIS

MLabs offers state-of-the-science blood testing for inherited (germline) mutations impacting both adult and pediatric [LINK to Pediatric Molecular Genetics page] patients. These molecular signatures are used to make the most precise diagnosis possible, guiding patient-specific plans for prevention, treatment and monitoring.

Analytical platforms include Sanger DNA sequencing for an extensive list of genes, SNP chromosomal microarrays, relative-quantitative PCR, methylation analysis, MLPA, mutation screening panels (xTAG, Luminex) and SNP testing.

Next-generation sequencing (NGS) modalities make it possible identify multiple genetic mutations with excellent sensitivity and broad coverage with one test, while preserving the integrity of a specimen.
 

NGS multi-gene germline panels are available for the following cancer types:

  • Breast and Ovarian Cancer
  • Colorectal Cancer
  • Endometrial/Uterine Cancer
  • Melanoma Cancer
  • Neurofibromatosis 
  • Pancreatic Cancer 
  • Paraganglioma Cancer
  • Prostate Cancer
  • Renal Cancer
  • Stomach Cancer

MOLECULAR AT ITS BEST

CUSTOMIZED NGS

Depending on the patient’s heredity, the best strategy may be a customized test for more than one genetic disease or syndrome. For those with the most extensive and complex familial cancer histories, we even offer a comprehensive 60+ gene panel. Our lab has the capacity to sequence nine samples simultaneously, extracting only the relevant data from more than 6,800 genes.

COMMITMENT TO QUALITY

You are only as confident in a diagnosis or treatment recommendation as you are in the pathology behind it. To earn that confidence, we back our work with industry-leading quality control. All raw data is approved by the lab director before it is included in a report, and all final reports are co-signed by the lab director and a geneticist/physician to ensure they offer the most appropriate, actionable clinical interpretation of test results.

BOARD CERTIFIED GENETICISTS

Our laboratory offers two ABMGG board certified Geneticists, Marwan Tayeh, PhD.; Jeffrey Innis, MD, PhD and a board certified Genetic Counselor. We are committed to assisting clinicians in identifying genetic aberrations to facilitate clinical diagnosis, management and genetic counseling.

EXPLORE MOLECULAR

GRAB A COMPLETE GUIDE


The molecular services brochure covers details about our genetic, molecular oncology and translational services. 

 

Consultation Brochure
Patient FAQ Computer Screen

QUESTIONS?

WE'VE GOT ANSWERS.

  • How do I order a test?
  • What are acceptable samples?
  • Where do I find results?
  • How can I order a specimen kit?