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Sequentify develops genomic samples processing products and technologies,  prior to sequencing hardware loading 

Novel library-prep solutions for Next-Gen Sequencing

The InfiniSeq™ Workflow

Pool your samples into one tube, right after the first step.

The ultimate solution for swift, effortless, and budget-friendly targeted NGS library preparation

The InfiniSeq Kit

Your science meets our simplicity.

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Cost effective

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Simple to use

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Automation friendly


Where We Fit into the Targeted Sequencing Workflow

Template extraction


Library prep

Target picking / Barcoding

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our technology


The InfiniSeq technology is agnostic to the sequencing platform

Secondary analysis

Mapping Alignment/ Noise reduction

Learn more about our
analysis pipeline

Tertiary analysis


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



Discover Our Current Selection of Panels


Dive Deeper into InfiniSeq

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


Contact us

Sequentify Ltd.
10 Moti Kind, St, 5th Floor, Rehovot, Israel 7638519

A few of our customers

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

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