Welcome to Zarqa Genomics Lab (ZGL), your trusted ally in unravelling the mysteries encoded within your patients’ DNA. As a premier genomics laboratory, we specialize in the sequencing and interpretation of genomic data to provide unprecedented medical insights.
Stands as an advanced genetic analysis technique gaining recognition as the preferred first-line genetic test in routine clinical settings. It transcends the limitations of targeted tests by encompassing coding and non-coding regions, along with mitochondrial DNA (mtDNA), thus offering a holistic view of your patients’ genetic landscape and optimizing diagnostic value.
Presents a comprehensive approach, meticulously sequencing the exons of all protein-coding genes alongside thousands of known disease-causing variants. Despite representing only 1-2% of the human genome, the exome harbours approximately 85% of known disease-related variants.
NGS analyses genes such as BRCA1 and BRCA2, shedding light on hereditary breast cancer susceptibility.
Identification of mutations in genes like MLH1, MSH2, and MSH6 provides insights into Lynch syndrome.
Mutations in the APC gene are scrutinized to understand the genetic basis of FAP.
NGS examines mutations in the CDH1 gene, which are linked to HDGC.
TP53 gene mutations are key markers analyzed through NGS to diagnose this syndrome.
RB1 gene mutations are explored to unravel the genetic foundation of retinoblastoma.
Genetic variations in MEN1 and RET genes are thoroughly investigated for their roles in MEN types 1 and 2.
Besides BRCA1 and BRCA2, other genes like PALB2, CHEK2, and ATM are analyzed for their roles in HBOC.
NGS examines NF2 gene mutations to elucidate the genetic basis of this disorder.
Genetic investigations focus on TSC1 and TSC2 genes, which are implicated in TSC.
RET gene mutations are key genetic markers examined for MTC.
Non-Invasive Prenatal Testing (NIPT), Genetic Carrier Screening, BRACA1/ BRACA2 Gene Panel, Paternity Testing, Sanger Sequencing Validation, Genetic Counseling, services of clinical scientist for choosing test, analyses on raw data, reanalyses on analysed report for deeper insights.
Sample types: saliva, blood, DBS cards, isolated DNA
TAT: All samples are processed within 45 working days
Zarqa Genomics is committed to empowering healthcare professionals like you with invaluable genetic insights to enhance patient care and improve health outcomes. Partner with us on the journey to personalized medicine and transformative healthcare solutions.
Discover our advanced genomic testing services tailored for your specific needs. Contact us today to enhance your research with unparalleled accuracy and expertise.
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