Sequentify: Your Complete End-to-End NGS Workflow
InfiniSeq™ Kit – Fast, Simplified Library Preparation
InfiniSeq™ Analysis Suite – Plug-and-Play NGS Insights
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Cost effective
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High-throughput
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Simple to use
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Automation friendly
Where We Fit into the Targeted Sequencing Workflow
Template extraction
DNA / RNA / cfDNA
Library prep
Target picking / Barcoding
Learn more about
our technology
Sequencing
The InfiniSeq technology is agnostic to the sequencing platform
Secondary analysis
Mapping Alignment/ Noise reduction
Tertiary analysis
Interpretation
What Makes Us Unique
Until just a few years ago, the most costly aspect of NGS was the physical sequencing of nucleotides. However, in recent years, there has been a proliferation of hardware companies in the market that have steadily reduced the cost of converting nucleotide sequences into data. Consequently, the bottleneck for reducing the overall cost of sequencing has shifted upstream. Today, in many cases, library preparation represents the most substantial expense for end users in the NGS process.
The demand for sequencing is steadily increasing, and it's evident that whole-genome sequencing isn't a one-size-fits-all solution. To make NGS a routine test in the healthcare sector and beyond, a significant reduction in the cost per sample is imperative. Sequentify's solution plays a pivotal role in paving the way for this future.
Enabling genomic diagnostics and therapeutics at a population-wide scale
Our Goal
What our customers are saying
Prof. Gil Atzmon,
Faculty of Natural Sciences, Haifa University
Sequentify's InfiniSeq targeted sequencing kit offered me a remarkably simple and highly cost-effective solution for sequencing my samples. Their bioinformatics pipeline proved invaluable, particularly as our lab had prior experience in NGS data analysis we appreciate the accuracy, completeness, reliability, and consistency of the results provided. It made the entire process seamless and efficient.
Nathali Kaushansky, PhD, Senior Staff Scientist, Weizmann Institute of Science
In our pursuit to uncover the genetic origins of Acute Myeloid Leukemia (AML) and other hematologic malignancies, we rely on InfiniSeq. InfiniSeq library prep solution is pivotal in scaling our genetic screening efforts, allowing us to efficiently process extensive sample sizes of hundreds to thousands of individuals. Its high-quality results make it an indispensable tool for cost-effective and large-scale genetic research in our laboratory.
Dr. Gabriel Rezonzew, MD,
Chief Operating Officer ODIN Bioscience
As we partnered with Sequentify, we tested their protocol in our facility. This has proven to be an invaluable tool that has helped us establish clear SOPs for our genomics program. The support from the Sequentify team has been remarkable; our laboratory swiftly positioned itself to successfully sequencing multiple 96-well plates per day. The panel they created for us delivers outstanding results, as we are currently implementing the automation of the entire process
Mention ISO13485 (link to section “Quality and accreditation” under Company page) (link to Company>Quality accreditation); Need to say clearly RUO as well; LOGO
Sequentify Ltd.
10 Moti Kind, St, 5th Floor, Rehovot, Israel 7638519
Sequentify is proud to be ISO13485 accredited.
All Sequentify products are designated as RUO and intended for research use only
Tailored for Every Genomic Laboratory
Catering to the Needs of All Genomic Labs: Effortlessly Replace Existing Workflows, Scale Up, and Boost Efficiency – A Perfect Fit, Even for Labs New to NGS
The Gordian Knot - Solution