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From reads  to reports....
we have you covered.

  • Designed to support sequencing lab workflows.
  • Reduces variant interpretation and reporting time from days to a few hours.
  • Based on first-hand experience interpreting variants from hundreds of genomes.

If you are interested in participating in our Early Access Program,

Literature
Curation
Bioinformatic
Data Curation

We provide around the-clock support Monday to Friday. Please call/email us and our support team will get back to you on priority.

Email: support@strandomics.com
Phone (USA): 1-800-516-5181
Phone (Worldwide): +1-650-288-4559

StrandOmics is HIPAA Compliant:
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Clinicians and Patients

We designed Strandomics after extensive interactions with practicing clinicians, patients, clinical interpreters, genetic counselors, and medical geneticists. Strandomics has now been used for analysis and reporting on many many cases, drawn from a growing list of more than 50 hospitals, including world renowned specialist centers in cancer, cardiology and ophthalmology as well as leading community hospitals (a few examples below). Several leading centers in the US are now using Strandomics as part of the Early Access Program.

Sequencing

Strand Centers, our genome sequencing arm in India, has used our platform to analyze hundreds of genomes spread over the following sequencing panels. In each case, Strandomics assisted our geneticists in shortlisting variants very quickly.

Variant Detection

Widely adopted Algorithms for Alignment and Variant Calling

Our variant detection algorithms have been used extensively in clinical applications.

For instance, click here to see how Wafergen Biosystem used our variant identification algorithms to validate their clinical assays.

And click here to see how the Sanford-Burnham institute used our variant identification algorithms to find the cause of a very rare disorder called CHIME disease.

And click here to see how a team of scientists from various Japanese medical schools used our variant detection algorithms to find a novel gene candidate for Andersen-Tawil syndrome.

And click here to see how the New York City Office of Chief Medical Examiner used our variant detection algorithms to study the cause of sudden unexplained death in a cohort of 274 individuals.

White papers that benchmarks our Alignment and Variant Calling algorithms with leading open source algorithms and show how our algorithms provide greater accuracy are available.

Comprehensive Variant Annotation

  • Is the variant in a conserved location?
  • Are there other known variants near the case variant?
  • What is the technical quality of this variant?
  • What are the Phenotypes associated with this disease?
  • Which diseases are associated with this gene?
  • What is the effect of the variant on a specific transcript of the gene?
All these and more... supported by a team of scientists curating the latest literature and incorporating public variant databases.

Effortless Interpretation and Reporting

The following statistic gathered in over a hundred cases says it all. When a significant pathogenic, likely pathogenic or strong VUS exists, we usually find it in under 5min using our simple point-and-click interface.

If you'd like to scale up this process, we support capture of comments and role-based access to enable reviews. And we support systematic SOPs to ensure consistency of comments. And we enable easy template-driven report compilation from your findings.

[ Download pdf ]

Strand was founded in 2000 by computer science and mathematics professors from India's prestigious Indian Institute of Science who recognized the need to automate and integrate life science data analysis through an algorithmic and computational approach. Strand's segue into the life sciences was through informatics products and services for research biologists, chemists, and toxicologists that combine advanced visualization, predictive systems modeling, data integration and scientific content management - over 2000 research laboratories worldwide (about 30% of global market share) are licensees of Strand's technology products, including leading pharmaceutical and biotechnology companies, research hospitals and academic institutions. With a recent investment by Biomark Capital, Strand has grown its established team to over 200 employees, many with multidisciplinary backgrounds that transcend computation and biology.

Since 2012, Strand has been expanding its focus to include clinical genomics, spanning sequencing, data interpretation, reporting and counseling in India. Strand operates a 10,000 square foot laboratory space with state of the art clinical genomics capabilities in India and is also establishing Strand Centers for Genomics and Personalized Medicine in several hospitals in India to serve as outreach points for genomic counseling.

For more information about Strand, please visit www.strandls.com,
or follow us on twitter @StrandLife.