Copy of GenoMed.kz

SESANA HK

COMPLEX SOLUTIONS FOR MOLECULAR BIOLOGICAL RESEARCH

ASIA PACIFIC AND CENTRAL ASIA

SESANA HK

One-stop shop
for LifeScience solutions

Quickly find next-generation sequencing and other solutions from our network of over lab.

One-stop shop
for LifeScience solutions

Quickly find next-generation sequencing and other solutions from our network of over lab.

OUR SERVICES

We offer a wide range of genetic testing services.

DNA and RNA extraction

NGS
Library Preparation

Sanger Sequencing and Fragment Analysis

High Throughput Sequencing

Microarray Analysis

Other Services

OUR BRANDS

We offer a wide range of instruments and reagents from leaders of LifeScience industry.

Genolab M

Opentrons

Thermofisher Scientific

BGI/MGI

Twist Bioscience

Other brands

OUR CLINICAL LABORATORY

We offer a wide range of clinical tests for reproductive health, cancer, inherited diseases, and healthy life.

Non Invasive prenatal testing

WGS, WES and targeted sequencing for diagnostics

Preimplantation genetic testing

Molecular karyotyping

Cancer profiling

Other tests

ABOUT GENOMED COMPANY

GenoMed, Kazakhstan is a subsidiary of Adoradum Genomics company, Australia. We work in the fastest-growing Asian countries - Kazakhstan, Uzbekistan, Kyrgyzstan, Mongolia, Tajikistan, Georgia, Turkmenistan, and others.
There is more than 100 million population who produce a lot of commodities, raw materials, and services. Our purpose is to bring modern molecular and genetic technologies there.

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

With the highest expertise in molecular biology, sequencing, microarray analysis, and more, we do more than just sell equipment. GenoMed, Kazakhstan 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 equipment and reagents for the full cycle of scientific research - from DNA extraction to bioinformatics analysis.

>10 YEARS OF EXPERIENCE

distribution division, scientific and medical products manufacturing, research and clinical laboratories

500 + PROJECTS

every year we delivered to our customers services, equipment and reagents

OVER 500 CUSTOMERS

government and private medical and research centers

150 000 TESTS

our clinical lab delivers to patients and partner medical centres

300+ SPECIALISTS

dedicated to improving health of our patients

200+ TYPES OF TESTS

state-of-the-art technologies microarray, NGS, metagenomics available at our lab

READY TO TALK?

The laboratory is located at:

050043, Kazakhstan, Almaty, Zhandosov street, 51

sales@geno-med.kz

Contacts

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

Next Generation Sequencing Library Preparation
We offer many different library preparation options:
- Whole Genome Sequencing
- Exome Sequencing
- Targeted Sequencing
- Amplicon Sequencing
- RNA Sequencing
- Diseases focused panels
- Others
- Fast turnaround times
- Ultra-low requirements
- Barcoded libraries
- Pooled libraries
- QC control
- Dry ice delivery
- Library storage

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.
- PCR product, purified or unpurified
- Plasmid, purified or bacterial clones
- Optional template purification
- Single-read service (96-well format only), verification sequencing
- Outstanding data quality with fast delivery
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.
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.
- Whole Genome Sequencing (WGS)
- Whole Exome Sequencing (WES)
- Targeted Sequencing/Panels (TCS)
- RNA sequencing and Spatial transcriptomics
- Single-cell sequencing
- Metagenomics
- Epigenomics
- Agrigenomics
- Genotyping by sequencing (GBS) services for SNP discovery
- ChIP-Seq
- Amplicon Sequencing
- MethylSeq
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
Microarrays are the best technique for genotyping and gene expression solution for many species
- Human Genotyping
- Non-Human Genotyping
- Methylation Analysis
- Genome-Wide Genotyping
- Targeted Genotyping
- Custom Genotyping
- Cytogenetic/copy number analysis
- Pharmacogenomics
- Microbiome Solutions
- Transcriptome profiling
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
- Biobanking
- DNA storage
- Bioinformatics
- Targeted sequencing panels design
- Cell cultivation
- Сytogenetic
- Metabolomic and proteomic
- Consulting
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.

Thermofisher Scientific

Thermo Scientific products help scientists around the world meet the challenges they face every day. From routine analysis to pioneering discoveries, the innovations help life scientists solve complex analytical challenges, empowering them to conduct the work they need to do, the way they want to do it.

Life Sciences

Antibodies
Cell Analysis
Cell Culture & Transfection
Cloning
DNA & RNA Extraction
Genome Editing
Epigenetics & ncRNA Research
Flow Cytometry
Gene Expression Analysis
& Genotyping
Microarray Analysis
Oligors, Primers, Probes
& Genes
PCR & Real-Time PCR
Protein Biology
RNAI
Sequencing
Stem Cell Research
Synthetic Biology

Applied Science

Agrigenomics
Animal Health
Bioprocessing
Biotech Company Solutions
Environmental
Chromatography
Drug Discovery & Development
Food & Beverage
Forensics
Mass Spectrometry
Materials Science
Microbiology
Pharma & Biopharma
Safety and Security
Threat Detection

Clinical & Diagnostics

Allergy Diagnostics
Anatomical Pathology
Autoimmune Diagnostics
Biobanking
Cancer Research
Clinical Microbiology
Cell & Gene Therapy
Clinical Genomics
Clinical Mass Spectometry
Clinical & Translational Research
Diagnostic Development
Diagnostic Testing
Hospital & Patient Care
Precision Medicine
Preclinical to Companion Diagnostic Development
Public Health

Lab Solutions

Chemicals
Lab Equipment
Lab Plasticware & Supplies
Sample Storage
& Management

Digital Solutions

Lab informatics
Connect Platform
Instrument Connectivity
Apps & Analysis Siftware
Lab Automation
Digital Services
Digital Commerce

MGI/BGI

MGI Tech Co is committed to building core tools and technology to lead life science through intelligent innovation. With a focus on R&D, production and sales of DNA sequencing instruments, reagents, and related products, MGI provides real-time, panoramic, and full-life-cycle equipment and systems for precision medicine, precision agriculture, precision healthcare and other relevant industries. MGI is a leading producer of clinical high-throughput gene sequencers, and its multi-omics platforms include genetic sequencing, medical imaging, and laboratory automation.

GEneMIND
Established in 2012, Shenzhen GeneMind Biosciences Co., Ltd. is headquartered in Luohu, Shenzhen, with over 8000 square meters of workplaces including R&D lab and GMP production line. Through years of assiduous efforts, GeneMind Biosciences has mastered various core techniques and processes of DNA sequencing platform, and developed research and production capability of key materials including enzyme, nucleic acid, and chip in China.
Genolab M
The high-throughput DNA sequencing system GenoLab M adopts the surface fluorescent sequencing technique (SURF-seq) based on chip amplification to identify the opytical signals of bases. Notably, with the unique “rolling mode” of GenoLab M, the second flow cell can be loaded and start working while the first flow cell is still running, and the two chips can produce data of different reads or sequencing types as required by the client, so as to shorten the waiting time, widen the scope of application, and bring unprecedented user experience.
GENOCARE 1600
The single-molecule DNA sequencing system Genocare 1600 adopts the surface restricted fluorescent sequencing technique (SURF-seq) and utilize the optical principle of total internal reflection to identify the optical signals of bases. Its sequencing-by-synthesis approach delivers speed, flexibility, high accuracy, and low-cost.

Opentrons

Opentrons makes robots for biologists. The company mission is to provide the scientific community with a common platform to easily share protocols and reproduce each other's results. The robots automate experiments that would otherwise be done by hand, allowing our community to spend more time pursuing answers to some of the 21st century’s most important questions.

Twist Bioscience

Twist Bioscience developed a proprietary semiconductor-based synthetic DNA manufacturing process featuring a high-throughput silicon platform that allows us to miniaturize the chemistry necessary for DNA synthesis. This translates into time and cost savings for our customers across their workflows. Researchers can access quality tools for more accurate NGS, highly customizable Gene Synthesis at scales that fit any workflow, more accurate genomic screens that require fewer resources, and libraries with optimized discovery power as every variant is directly synthesized.

Genes

Clonal Genes
Gene Fragments

Oligo Pools

NGS
Custom Panels
Alliance Panels
Fixed Panels
Exome 2.0
Human Comprehensive Exome
Human Core Exome
Human RefSeq Panel
Mitochondrial Panel
Mouse Exome Panel
Respiratory Virus Research Panel
SARS-CoV-2 Research Panel
SARS-CoV-2 NGS Assay-EUA
Comprehensive Viral Research Panel

Library preparation

Enzymatic Fragmentation Kit
Universal Adapter System
UMI Adapter System
Twist 96-Plex Library Prep Kit

Reagents & Kits
Fast Hybridization and Wash Kit
Standard Hybridization and Wash Kit
Universal Blockers
Methylation Detection System

Controls and Standarts
SARS-CoV-2 RNA Controls
Respiratory Virus Controls
cfDNA Pan-cancer
Reference Standards

Synthetic Controls

Liquid Biopsy
cfDNA Pan-cancer
Reference Standards

Infectious Disease
SARS-CoV-2 Controls
Respiratory Virus Controls

Antibody Discovery
High throughput antibody production

Antibody Services
Antibody Discovery
Antibody Optimization
Partnership & Collaborations
Pipeline & Licensing

SARS-CoV-2 Tools

SARS-CoV-2 NGS Assay-EUA

Fixed Panels
SARS-CoV-2 Research Panel

Synthetic Controls
SARS-CoV-2 RNA Controls
Respiratory Virus Controls

Catalog Antibodies
Anti-ACE2
Anti-SARS-CoV-2 S1

Controls and Standarts
Combinatorial Variant Library
Spread Out Low Diversity Libraries
Site Saturation Libraries

Other Brands

We are a distributor of life science products throughout Central Asia. Our portfolio is representative of some of the best manufacturers in the business across the disciplines of genomics, protein science, cell biology and automation. Each of our suppliers is a company which is dedicated to supplying the highest quality products and to serving the needs of their customers. We believe our suppliers each provide products which offer our customers value for money, the highest quality and excellent performance.

SWIFT bioscience
Isohelix
Assay Designs
Epichem

NEST
BioActs
Immundiagnostik

GeneMind
Antibodies Incorporated
Cell Technology
RD-Biotech

Non Invasive prenatal testing
We offer most popular and accurate non-invasive prenatal testing
Panorama test, NATERA, USA
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 test, BGI, China
- 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.

WGS, WES and targeted sequencing for diagnostics

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

TESTS

Panels
Whole Exome Sequencing
Single Gene Tests
Variant Specific Testing

PANELS

Cardiology
Dermatology
Ear, Nose & Throat
Endocrinology
Gastroenterology
Hematology
Hereditary
Cancer
Immunology
Malformations
Metabolic Disirders
Mitochondrial Disorders
Nephrology
Neurology
Ophthalmology
Pulmonology

SERVICES

Expansion services
Customization if Diagnostic Panels
Re-evaluation and Re-analysis Service
Clinical Genetics Support

FREQUENTLY ORDERED

Whole Exome Family Plus
My Retina Tracker Program Panel
Retina Dystrophy Panel
Aorta Panel
Cardiomyopathy Panel
Comprehensive Epilepsy Panel
Hypertrophic Cardiomyopathy (HCM) Panel
Primary Immunodeficiency (PID) and Primary Ciliary Dyskinesia (PCD) Panel
Familial Variant Testing

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.
- Preimplantation genetic testing "PGT-A"
- Preimplantation genetic testing "PGT-SNP"
- Non-invasive preimplantation genetic testing "niPGT"
- Determining the relationship of the embryo
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.
- Establishing the origin of the chromosomal imbalance found in the embryo
- Analysis of endometrial receptivity "ERT-test"
- Preimplantation genetic diagnosis of monogenic diseases (PGT-M)
- Non-invasive preimplantation genetic testing "PGT-A + niPGT"

Molecular karyotyping
The innovative oligonucleotide-based microarrays, these solutions have been specifically designed, developed and validated by cytogeneticists for cytogeneticists performing molecular karyotyping.
- Postnatal diagnostics microdeletion syndromes
- Prenatal diagnostics microdeletion syndromes
- Miscarriage diagnostics
- Loss of heterozygosity detection and Uniparental disomy diagnostics.
- Increased Detection Rates
- Faster Results at Lower Costs
- Streamlined Processes
- Support from Sample-to-result
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
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.
- Screening
- Diagnosis and Prognosis
- Treatment Planning
- Monitoring

Other tests
GenoMed offers wide range of genetic and other tests for many clinical areas
- Wellness and Nutrition test
- Pharmacogenetics
- Inherited diseases carrier screening
- Fertility test
- Paternity test
- Ancestry test
- Fluorescent hybridization in situ (FISH)
- Immunohistochemistry (IGH)
- Anatomical pathology tests
- Allergy tests