The Clinical Exome Sequencing & Hemolytic Uremic Syndrome test examines 7000 genes covering exons and targeted regions such as atypical hemolytic uremic syndrome (aHUS) genes. Decipher the presentations of aHUS through testing to discover the complex system of genes that stem this disease.
Advanced Genomics Laboratory
Peripheral Blood
Comprehensive Genomic Analysis
Expert Interpretation
Clinical Exome Sequencing examines more than 7000 genes while providing targeted analysis of key genes associated with atypical Hemolytic Uremic Syndrome (aHUS).
Comprehensive sequencing of protein-coding regions covering clinically relevant genes associated with rare and inherited disorders.
Working together with experienced nephrologists and leading healthcare institutions to deliver comprehensive genetic testing.
Consultant Nephrologist
Consultant Nephrologist
From blood sample collection to expert clinical interpretation, our streamlined genomic workflow ensures accurate identification of clinically relevant genetic variants associated with rare inherited disorders and atypical Hemolytic Uremic Syndrome.
Peripheral blood sample is collected for comprehensive genomic analysis.
High-quality genomic DNA is extracted from the collected sample.
Sequencing of DNA coding regions using advanced NGS and MLPA technologies.
Identification of clinically relevant genetic variants associated with rare disorders and aHUS.
Experienced clinical geneticists interpret sequencing data and correlate findings.
Comprehensive report delivered within 19 Working Days.
Enable faster and accurate diagnosis to guide treatment and boost clinical decision-making.