Today we wanted to share a recent client case study to demonstrate how VarSeq has been implemented in a CLIA certified clinical laboratory. Please feel free to contact us if you have questions or if you would like to discuss VarSeq further at firstname.lastname@example.org.
It is standard practice for newborns to be screened for genetic diseases before leaving the hospital to assess for serious medical conditions that, left untreated, can cause lifelong health problems or in some cases, early death. What is not standard is which and how many conditions are screened for in each state. And in many states, the number of conditions screened simply isn’t enough.
This means there are children all over the United States who are not being screened for serious genetic diseases they may have. By the time parents or physicians recognize the condition, serious, sometimes irreparable damage may already have been done. Baby Genes, a CLIA certified clinical laboratory formed in 2013 in Colorado, is trying to change this.
The mission at Baby Genes is to save lives by standardizing the approach to newborn screening (NBS) with a more comprehensive genetic sequencing-based test that screens for more conditions and provides more actionable information.
Using next-generation sequencing assays focused on NBS, Baby Genes is able to provide parents and physicians with screening results quickly. An earlier diagnosis means that a treatment plan can come together sooner and more innocent lives can be saved.
Dr. Angie Purvis, Associate Laboratory Director and Clinical Research Lead at Baby Genes, has been a part of the development of this test. She emphasized the importance of a more comprehensive test that provides better information. She states, “We are really looking at this from the perspective of, if this was my baby, what kind of information would I want? Of course, I want the best information available. And that’s what we are trying to give people.”
The current standard for newborn screening uses biochemical testing for various genetic, metabolic and rare diseases. Purvis explained how Baby Genes wants to revolutionize the testing to look at newborns earlier on for genetic diseases. The earlier these rare disorders are detected, the better the outcome for the affected newborns. The idea of harnessing the power of genetics is ideal in this process as it provides a faster, more comprehensive test over waiting for slower biochemical tests to be run, which can save more lives.
And this is Baby Genes’ main emphasis; to take newborn screening out of the biochemical lab and put it into a new millennium of genomics. Using next-generation sequencing, Dr. Purvis and the rest of the team have created a genetic test that includes full exon sequencing of the genes associated with various conditions and diseases. Next-generation sequencing allows the team at Baby Genes to determine if a newborn has a mutation that is clinically linked to one of these genetic disorders. Golden Helix’s VarSeq software has been instrumental in the development of this test. “Not only has it been valuable to speed up the process of sifting through large, complex genomic data sets, but also for initial quality control”, said Dr. Purvis.
The goal of a standardized NBS is to take a genetic approach and make it accessible. This requires two major factors be met to fulfill the Public Health Program’s demands; one is to be low cost, and two is to be quick. So far, Baby Genes has made significant progress in developing a faster test.
The team has shortened the turn-around time to only 48-96 hours from the time the sample arrives at the laboratory to the return of the genetic data back to physicians. “We’ve found VarSeq to be user-friendly and highly rational. It really simplifies our entire process and makes it go much faster.” Now, Baby Genes is working on lowering the cost of this procedure to make it available to everyone.
Ultimately, a newborn screening panel that is comprehensive and standardized can save more lives. As the challenges of creating a cost-effective and a quick testing process are overcome, the accessibility of a genetic screening approach to more parents and physicians increases.