Enabling deep sequencing of over 6,000 patients cohort using an ultra-fast and cost effective targeted sequencing NGS panel 31 Oct 2022, Rehovot, Israel
Sequentify announced its collaboration with Yeda, the commercial arm of the Weizmann
Institute of Science (WIS) and NIH, as part of a grant to sequence over 6,000 patients using the
Sequentify Myeloid NGS panel, offering cost-effective, high throughput NGS sequencing at
As part of the collaboration, Dr. Liran Shlush from the Weizmann Institute will use Sequentify’s
high throughput Myeloid panel to sequence over 6,000 patients to evaluate the hypothesis that
age-related clonal hematopoiesis may play a role in the progression of mild cognitive
impairment and kidney function decline.
Sequentify’s Myeloid NGS genetic panel enables diagnostics, screening and prediction of
blood-derived cancers such as MDS, AML, MPN, CMML and JMML.
Based on Sequentify’s patent-pending InfiniSeq technology, Sequentify’s Myeloid panel enables
hospitals, genomic labs and oncology clinics to implement fast, automation-friendly and
cost-effective diagnostics and screening, providing oncologists with a same-day response
enabling them to perform patients’ diagnostics and whole population screening to detect early
The InfiniSeq technology enables library preparation as a one-pot reaction in 4 steps within 3.15
hours and involves 40 minutes of hands-on time allowing easy implementation by healthcare
providers in a single shift (morning to noon). This means fewer employees are needed, less
training required, the pricing supports mass market implementations. Furthermore, the
technology enables scalability from sequencing a few patients to performing whole population
screening, keeping costs low and turnover time fast.
Together with the Myeloid panel, Sequentify offers its analysis pipeline to easily and rapidly
determine variants, running on-site in the hospital or lab, saving cloud costs and maintaining
"We are happy to collaborate with the Weizmann Institute of Science, through its commercial
arm, Yeda, on Myeloid research using Sequentify’s Myeloid panel for the research of CKD and
cognitive impairment in elderly people”, said Tamir Biezuner, CSO and Co-founder of
Sequentify. "Sequentify’s Myeloid panel offers universities, hospitals and research labs an easy
pathway to implementation of NGS for myeloid-related disease with unparalleled ease and
affordability, and aligns with our mission of democratizing genomics and enabling diagnostics,
screening and prediction at scale."
"Mild cognitive decline and chronic kidney disease (CKD) are global health problems that have
reached epidemic proportions, disproportionately affecting the elderly population, and its
prevalence is rising rapidly in older adults.”, said Prof. Liran Shlush, PhD MD at the Weizmann
Institute. "The ability to perform targeted sequencing across large cohorts easily and
cost-effectively using Sequentify’s technology now enables affordable performance of such
The Sequentify Myeloid NGS panel is for Research Use Only (RUO). It is not intended for use in
Sequentify now offers free samples of its Myeloid panel for evaluation by healthcare
organizations. Contact Sequentify for more details.