LEANGENE partners with Illumina; the global leader in DNA Sequencing and array-based Technologies.

This partnership entitles LeanGene to promote and support Illumina full portfolio in Jordan and Iraq through dedicated team certified by illumina to be closer to you more than ever with all innovative solutions and support for all of your needs. 

Illumina has pioneered major advances for sequencing platform simplicity, flexibility, and performance. Sequencing output has grown over a thousand-fold, from less than 1 gigabase to 6 terabases per run, while the number of reads has increased from millions to billions.

Experiments that once required complex workflows now use simple push-button sequencing!

Illumina NGS instruments have been adopted by leading institutions around the globe, both big and small, and are the production platform for all major genome centers.

Whether your studies require a broad review of the genome or in-depth, base-by-base interrogation of a particular loci, Illumina offers total solutions designed to help you generate more complete answers, as efficiently and effectively as possible. Have confidence in your data, knowing that Illumina sequencing by synthesis (SBS) technology has been used to generate >90% of the world’s sequencing data.*

*Data calculation on file, Illumina, Inc. 2015.

DNA Sequencing

DNA Sequencing

Discover the entire genome with whole-genome solutions, or focus on specific regions of interest with whole-exome and targeted sequencing options.

Unlimited areas of discovery including, Cancer Genomics, HLA Typing, Forensic Genomics, Plant and Animal Sequencing, Inherited Condition Screening, Causal Variant Discovery, Microbial Sequencing, Mitochondrial Sequencing, and many more.

RNA Sequencing

RNA Sequencing

Take advantage of a broad range of sequencing techniques for targeted RNA or whole-transcriptome studies.

RNA-Seq allows researchers to detect both known and novel features in a single assay, enabling the detection of transcript isoforms, gene fusions, single nucleotide variants, allele-specific gene expression and other features without the limitation of prior knowledge.

Methylation Sequencing

Methylation Sequencing

Enhance epigenetic studies with high-coverage density and flexibility enabled by sequencing-based DNA methylation analysis.

With Methylation sequencing, scientits are able to discover epigenetic alterations in cancer and understand the functional mechanisms at work in complex disease cases.

Library Preparation Solutions

Library Preparation Kit Selector

Illumina offers comprehensive sequencing library preparation solutions for a wide variety of NGS methods, including whole-genome sequencing, targeted DNA sequencing, whole-transcriptome sequencing, targeted RNA sequencing, and more. These solutions support a variety of sample types, from cell lines to fresh tissue, formalin-fixed paraffin-embedded (FFPE) samples, blood, and other challenging sample types.

Illumina library prep protocols can accommodate a range of throughput needs, from lower-throughput protocols for small laboratories to fully automated library preparation workstations for large laboratories or genome centers.

Sequencing Platforms

Illumina PlatformsIllumina innovative next-generation sequencing (NGS) platforms deliver exceptional data quality and accuracy, at a massive scale. From benchtop to production-scale sequencing systems, you’ll find the right platform to advance your research. 

Determine the best benchtop sequencer or production-scale NGS platform to transform your lab, depending on the application that you will use more frequent, your lab throughput and your budget.

Call us today to help you choose the Sequencing System that best fits your needs!  

Ask Our Specialists!



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LEANGENE For Medical & Electronic Supplies

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T:+962-6-46-55401 | F:+962-6-46-55402 

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