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SAN DIEGO , Oct. 27, 2021 /PRNewswire/ -- Illumina, Inc. (NASDAQ: ILMN ) today announced an agreement with Israel's Ministry of Health (MoH) for a pilot program to implement the use of whole-genome sequencing (WGS) in critically-ill infants suspected of having a genetic disorder in neonatal intensive care units (NICU). The program, led by the Genetics Institute (Tel-Aviv Sourasky Medical Center), will evaluate the use of WGS in routine care as an effective first-tier diagnostic tool to enable faster identification of disease-causing genetic abnormalities in infants, aiding their clinical care and management.
The 18 hospitals participating in the program will enroll newborns from day 0 to day 90 of life who are admitted to a NICU with a clinically suspected genetic disorder, along with their biological parents. The pilot will begin this month and enrollment will run for up to 24 months, with patients being followed for a total of 180 days after recruitment. This project will lead to the creation of national reimbursement for WGS as a diagnostic tool in hospitals across Israel .
"Evidence from other countries shows that whole-genome sequencing offers significant benefits for the diagnosis of suspected genetic disease in critically-ill infants. Based on this international experience, our aim is to implement and provide this approach as a diagnostic assay in all neonatal intensive care wards, ideally replacing the routine diagnostic tests currently used," said Dr. Amihood Singer, Head of Community Genetics Department at the Ministry of Health, Israel .
"We are proud to work with the Ministry of Health and the Tel Aviv Sourasky Medical Center to implement whole-genome sequencing to accelerate the diagnoses of critically-ill infants with suspected genetic disease," said Phil Febbo , MD, Chief Medical Officer at Illumina. "This program will help speed the time to definitive diagnosis for these children thereby decreasing the uncertainty for their families, improving the management for the children, and reducing the need for unnecessary iterative tests and longer stays in the NICU."
WGS is the most comprehensive method for genetic disease testing and allows identification of pathogenic variants in non-coding regions as well as unprecedented detection of disease-causing copy number and structural variants. WGS accelerates time to diagnosis for patients with suspected genetic diseases, helping inform optimal management options beyond those based solely on conventional approaches such as nonspecific phenotypic presentation.
Illumina will provide Illumina® DNA PCR-Free Prep reagents for library preparation of DNA and sequencing reagents for 375 WGS samples (125 trios) using the latest NovaSeq TM 6000 S1 v1.5 Reagent Kit.
Illumina is improving human health by unlocking the power of the genome. Our focus on innovation has established us as the global leader in DNA sequencing and array-based technologies, serving customers in the research, clinical and applied markets. Our products are used for applications in the life sciences, oncology, reproductive health, agriculture and other emerging segments. To learn more, visit www.illumina.com and connect with us on Twitter , Facebook , LinkedIn , Instagram , and YouTube .
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SOURCE Illumina, Inc.