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Whole Exome Sequencing (WES)

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Unlock the Genetic Code with Whole Exome Sequencing (WES)

At Sapiens Genetics, we offer a pioneering approach to genetic diagnostics through our Whole Exome Sequencing (WES) service. WES enables a comprehensive analysis of the protein-coding regions of all nuclear and mitochondrial genes (~20,000) within the human genome. While these regions make up only about 1% of the entire genome, they harbor approximately 85% of disease-causing mutations, making WES one of the most powerful tools in the identification of genetic disorders.

What is WES and Why is It Important?

Whole Exome Sequencing (WES) is a sophisticated genetic test that focuses on the exome—the protein-coding regions of the genome. These regions are critical as they contain the genetic instructions that influence the development, growth, and overall health of an individual. By examining the exome in detail, WES identifies mutations that could lead to various genetic disorders, providing valuable insights into complex and rare conditions.

Our WES Service:
Who Can Benefit from WES?

WES is particularly beneficial for individuals with:

Complex Phenotypes:

Those with symptoms that suggest multiple possible diagnoses.

Genetically Heterogeneous Disorders:

Conditions that can be caused by mutations in different genes.

Suspected Genetic Disorders:

Cases where a specific genetic test is not available.

Inconclusive Previous Genetic Testing:

Individuals who have undergone genetic testing before but did not receive a definitive diagnosis.

What Sets Us Apart?

At Sapiens Genetics, we are committed to delivering the highest standards of genetic analysis through our WES service. Here’s what makes our WES offering unique:

High-Quality Sequencing:

We provide robust and uniform sequencing data with an average coverage of 154x at 100M sequencing reads, ensuring that over 99.6% of base pairs are covered at least 20x.

Mitochondrial Genome Sequencing:

Our service includes sequencing of the mitochondrial genome (mtDNA) with a mean coverage of 9362x, ensuring comprehensive detection of mutations.

State-of-the-Art Bioinformatics:

Our in-house bioinformatics pipeline ensures precise data analysis, with a focus on accuracy and reliability.

Expert Interpretation:

Our team of geneticists and clinicians provides thorough and insightful interpretations, utilizing the latest scientific research and databases.

Comprehensive Reporting:

We deliver detailed, easy-to-understand reports that help healthcare providers make informed decisions about patient care.

Rapid Turnaround:

We ensure that results are available within 6 weeks, enabling timely interventions.

Optional Secondary Findings Analysis:

We offer optional analysis of secondary findings based on the latest ACMG guidelines.

Why Choose Sapiens Genetics for WES?

Sapiens Genetics stands out with its commitment to excellence in genetic testing. Our WES service not only provides detailed analysis but also offers added benefits like the optional analysis of clinically relevant non-coding variants and improved coverage of challenging genes. We believe in transparency, accuracy, and delivering results that truly make a difference in patient care.

Perfect WES Quality Score:
2.00 / 2.00

Our WES service achieved a top score in external quality assessment by GenQA.

Need more information?

For more information or to schedule a genetic counseling appointment, please contact us.

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