DNA Extraction:

• Cells, eukaryotic: blood cells, cultured cells, tissue cells (fresh/frozen), pathogens
• Cells, prokaryotic: bacteria, virus
• FFPE
• Body fluids: serum, plasma, urine, cell media, buccal swabs, saliva, cerebral spinal fluid, stool, and other cell–free body fluids
• Environmental samples
• Plants
• Ancient materials
• Other

RNA Extraction:

• Cells, tissue
• Blood
• Biofluids (e.g., plasma, serum)
• Formalin-fixed, paraffin-embedded (FFPE), laser capture microdissection (LCM), fine needle aspirate biopsies (FNAB)
• Others

We offer DNA extraction and storage service. Column and magnetic beads technology. Up to 1000 samples per day

DNA and RNA extraction

We offer many different library preparation options:

Next Generation Sequencing Library Preparation

Sanger Sequencing
and Fragment Analysis

High Throughput
Sequencing

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The data included in our reports for every sequence are Phred20 analysis, *.ABI and *.scf trace files and seq files in text format. Verification sequencing reports provide the following: insertions, deletions, mismatches between reference sequence and sequencing data, and alignment between reference sequence and sequencing data.

Sanger Sequencing and Fragment Analysis

Sanger sequencing is used to study a small subset of genes linked to a defined phenotype, confirm next-generation sequencing (NGS) variants, detect minor allele fractions down to 5%, or read contiguous sequences up to 1,000 bases.

Fragment analysis is a powerful technique with simple, straightforward workflows and used in a wide-range of applications, such as detection of mutations, genotyping, identification of short tandem repeats, and gene expression profiling.
We use Applied Biosystems genetic analysis systems - a trusted standard for Sanger sequencing and fragment analysis by capillary electrophoresis

High Throughput Sequencing

GenoMed laboratory operates a suite of sequencing instruments, including Illumina MiSeq and NextSeq 500, MGI and 10x Genomics Chromium. We provide sequencing as a service to external researchers on unlimited basis.

Our genome sequencing service helps meet a wide range of research goals. Whole Genome Sequencing (WGS) can be applied in disease research as well as in population evolution studies. Target Capture Sequencing (TCS) can be effectively utilized for the in-depth analysis of exons (protein-coding regions of the genome) and genes of interest. As De novo sequencing offers genome assembly and annotation for seldom studied species and species with incomplete reference genomes, it provides a great advantage for plant, animal, and microbial evolution research. We accept ready for sequencing libraries and provide fast and accurate sequencing. One library or hundreds of libraries - it is all possible.

Microarray Analysis

Other Services

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Microarray Analysis

Microarrays are the best technique for genotyping and gene expression solution for many species

The Axiom Genotyping Solution provide researchers with powerful genotyping tools to identify, validate, and screen complex genetic traits in human, plants, animals or micobes. It includes arrays with genotype-tested content from the Axiom Genomic Database or de novo markers that are important to you. The complete solution comprises genotyping arrays, reagent kits, a fully automated workflow, and easy-to-use free data analysis tools. Customize your genotyping array or panel for any high-throughput industrial application with confidence that all of your markers of interest can be targeted and manufactured on the custom array.

Other Services

We offer a range other services in molecular biology and NGS areas

Our life science laboratory services provide you with an international reach and employ the latest technology and methodologies – so that you get the most accurate and reliable results. Our expert staff is trained to the highest standards and has an in-depth knowledge of their fields and your business needs. We provide experience in meeting both international and local regulations for a wide range of industries.

Non Invasive prenatal testing

WGS, WES and targeted sequencing for diagnostics

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Panorama test, NATERA, USA

NIFTY test, BGI, China

Non Invasive prenatal testing

Panorama is a blood-based genetic, prenatal screening test of the pregnant mom that screens for common chromosomal conditions that affect a baby’s health. Panorama uses unique SNP-based technology to deliver the most accurate non-invasive prenatal testing on the market.
Panorama can be performed as early as nine weeks gestation. Most results will be returned to your doctor within 5-7 calendar days.

NIFTY is a highly accurate, non-invasive prenatal screening that uses a blood sample from the pregnant mother to detect chromosomal abnormalities in the fetus. NIFTY is available from as early as the 10th week of pregnancy and can screen for a range of chromosomal abnormalities in both singleton and twin pregnancies, such as Down Syndrome (Trisomy 21) and Edwards Syndrome (Trisomy 18), and other chromosomal abnormalities that could affect a baby’s health.

We offer most popular and accurate non-invasive prenatal testing

TESTS

PANELS

SERVICES

FREQUENTLY ORDERED

Panels

Cardiology

Whole Exome Family Plus

Expansion services

Whole Exome Sequencing

Dermatology

My Retina Tracker Program Panel

Customization if Diagnostic Panels

Single Gene Tests

Ear, Nose & Throat

Retina Dystrophy Panel

Re-evaluation and Re-analysis Service

Hematology

Comprehensive Epilepsy Panel

Malformations

Familial Variant Testing

Variant Specific Testing

Endocrinology

Aorta Panel

Clinical Genetics Support

Hereditary Cancer

Hypertrophic Cardiomyopathy (HCM) Panel

Metabolic Disirders

Neurology

What to Order?

Gastroenterology

Cardiomyopathy Panel

Immunology

Primary Immunodeficiency (PID) and Primary Ciliary Dyskinesia (PCD) Panel

Mitochondrial Disorders

Ophthalmology

Nephrology

Pulmonology

WGS, WES and targeted sequencing for diagnostics

Sequencing, data analysis, varialt calling, ACMG classification and clinical interpretation according to patient phenotype.

Preimplantation genetic testing

Molecular karyotyping

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Preimplantation genetic testing

Pre-implantation Genetic Testing (PGT) is a sophisticated scientific technique which can be used to test embryos for either a specific known single gene condition or chromosome variation.

This enables only chromosomally healthy embryos or those unaffected by a specific disorder to be selected for transfer during an IVF cycle, maximising the chance of a healthy baby.

Molecular karyotyping

The innovative oligonucleotide-based microarrays, these solutions have been specifically designed, developed and validated by cytogeneticists for cytogeneticists performing molecular karyotyping.

Molecular cytogenetics plays an important role in the characterization of chromosome anomalies and is a critical component of current genetic studies including research into both constitutional disorders and cancer. GenoMed is bringing the newest molecular techniques to cytogenetic laboratories. Our innovative methodologies support:

Cancer profiling

Other tests

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GenoMed is determined to help you identify the ideal treatment path using the right test so you can deliver the best possible outcomes based on the most relevant data.

Cancer profiling

Other tests

GenoMed offers wide range of genetic and other tests for many clinical areas

About SESANA company

SESANA, Hong Kong has subsidiaries - Adoradum Genomics company, Australia and Genomed company, Kazakhstan. We work in the fastest-growing Asian countries - Kazakhstan, Uzbekistan, Kyrgyzstan, Mongolia, Tajikistan, Georgia, Turkmenistan, Philippines, Indonesia, Malasia, Vietnam, Thailand and others.
There is more than 700 million population who produce a lot of commodities, raw materials, and services. Our purpose is to bring modern molecular and genetic technologies there.

Adoradum Genomics, Australia offers professional support, and advice on the selection of equipment and reagents, implementation, and maintenance of methods and technologies. Turning to us, you will always receive advice from specialists with practical experience in using the equipment that we sell.

Representing a wide range of leading brands in the field of Life Science, we can offer the full cycle of scientific research - from DNA extraction to bioinformatics analysis.

GenoMed, Kazakhstan includes a distribution division, the production of scientific and medical products, as well as service and clinical laboratory.

With the highest expertise in molecular biology, sequencing, microarray analysis, and more, we do more than just sell equipment.

LOW PRICE

HIGHLY QUALIFIED TEAM

We offer you products at the most reasonable and competitive price. We are ready to back up long-term cooperation and loyal partnership with an even more favorable price offer.

In collaboration with world leaders, we provide over
100 comprehensive laboratory services for research projects