Delve into Fore Genomic's groundbreaking research in genomics. Learn how our research initiatives drive innovation in precision medicine, disease understanding, and next-generation therapeutic solutions.
Research
Newborn sequencing—a groundbreaking technology that offers a comprehensive analysis of an infant’s genome shortly after birth—has revolutionized our understanding of human health. Traditionally used to diagnose genetic disorders and rare...
Research
Newborn screening is a crucial healthcare process that helps in identifying potential health issues in newborns before any serious symptoms appear. In California, this process is designed to safeguard the health of infants, providing parents with peace of...
Research
Each year, thousands of children are hospitalized due to severe drug reactions (ADRs). This can be dangerous for the child, scary for the parent or caregiver, and unnerving to the hospital staff. In addition to the stress and medical issues, healthcare...
Research
There has been an increase in the use of egg, sperm, and embryo donation services over the last few decades. This has been a huge boon to couples who want a family but are unable to conceive naturally. Donor eggs and sperm are especially wonderful options...
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In the United States, over 30 million people live with rare or undiagnosed diseases, often facing long wait times and high medical costs to find answers. But with Fore Genomics testing, you can eliminate the hassle and get peace of mind...
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Healthcare: Struggling with a One-Size-Fits-All Approach:The current healthcare system is facing significant challenges. Many individuals struggle to find effective treatment due to a one-size-fits-all approach that fails to consider individual differences1. A...
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The future of newborn screening is on the horizon, with groundbreaking technology like Fore Genomics leading the way. A recent study in the Journal of the American Medical Association surveyed rare disease experts to explore their views on implementing...
Product | Research
As a new or expecting parent, you may be considering genetic health screening for your child to help identify potential health issues. While traditional genetic screenings such as carrier screening, NIPT (non-invasive prenatal testing), and newborn...
Research
Our body is made up of billions of cells, and in each cell there are instructions, called genes, that make all the necessary structural components and chemicals for the body to work.A variation in a gene that causes the gene to not work properly is...
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Hey there, new parents! I bet you never thought you'd be diving deep into genetic research when you were daydreaming about your new little one. But here's the thing - some brilliant scientists at Revvity have made a fascinating discovery that...
Research
Welcoming a new child into the family invites a world brimming with hopes, dreams, and aspirations for their future. However, some parents face an unexpected, challenging journey - traversing through the complex realm of rare diseases. Genetic testing can...
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A particular study was published in Science Direct that compared two kinds of DNA testing methods, called Whole-Exome Sequencing (WES) and Whole-Genome Sequencing (WGS), to see which is better for diagnosing rare diseases in both children and...
Research
Newborn screening is the process of testing newborns for specific genetic, metabolic, endocrine and other disorders shortly after birth.Its aim is to catch health issues early on, allowing for quick intervention to prevent serious complications. This early...
Product | Research
Healthcare, with its foundation in standardized protocols and norms, occasionally confronts cases that veer off these well-trodden paths. The journey of Jessica and Sophie powerfully exemplifies this, shedding light on both a gap in our healthcare system and...
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The birth of a baby, brimming with vitality, often fosters the comforting belief that a healthy infancy naturally progresses into an equally robust childhood. This assumption, however, is not fail-proof, as the odyssey of Jessica and her daughter Sophie...
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In the joyous journey of parenting, welcoming a child symbolizes a moment filled with hope and dreams. As Jessica cradled her new baby, Sophie, cherishing the unique euphoria of those first days, she, like many parents, trusted the healthcare system to...
Product | Research
What can your DNA tell you about your future health? An understanding of genetics is the foundation of precision medicine and personalized healthcare. Genetic testing is powerful, and incredibly versatile, for many stages of screening and detailed...
Research
When it comes to your children’s health, you want them to receive the best care and attention from medical professionals. When evaluating any medical decisions that require a laboratory for testing, you expect the lab to be up-to-date with the...
Product | Research
Precision medicine, also called personalized medicine, is a growing trend in healthcare. Historically, medical guidelines are based on studies that look at the average person. But the science doesn’t take into account the outliers. Evidence-based...
