DNA and RNA extraction

Next Generation Sequencing
Library Preparation

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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.

Thermofisher Scientific

BGI/MGI

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Life Sciences

Applied Science

Clinical & Diagnostics

Lab Solutions

Digital Solutions

Antibodies

Agrigenomics

Allergy Diagnostics

Chemicals

Lab informatics

Cell Analysis

Animal Health

Anatomical Pathology

Lab Equipment

Connect Platform

Cell Culture & Transfection

Bioprocessing

Autoimmune Diagnostics

Lab Plasticware & Supplies

Instrument Connectivity

Cloning

Biotech Company Solutions

Biobanking

Sample Storage
& Management

Apps & Analysis Siftware

Lab Automation

Digital Services

Digital Commerce

DNA & RNA Extraction

Cancer Research

Genome Editing

Environmental

Clinical Microbiology

Microarray Analysis

Food & Beverage

Clinical & Translational Research

Oligors, Primers, Probes & Genes

Forensics

Diagnostic Development

PCR & Real-Time PCR

Diagnostic Testing

Protein Biology

Hospital & Patient Care

Mass Spectrometry

Precision Medicine

RNAI

Materials Science

Preclinical to Companion Diagnostic Development

Sequencing

Microbiology

Public Health

Stem Cell Research

Pharma & Biopharma

Synthetic Biology

Safety and Security Threat Detection

Epigenetics & ncRNA Research

Chromatography

Cell & Gene Therapy

Flow Cytometry

Drug Discovery & Development

Clinical Genomics

Gene Expression Analysis
& Genotyping

Clinical Mass Spectometry

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.

Sequencers

Sequencers

Sequencers

Sequencers

Product Model

Features

Applications

Flow Cell Type

Lane/Flow Cell++

Operation mode

Max. Throughput / RUN

Effective Reads / Flow Cell

Average run time

Min. Read Length

Max. Read Length

DNBSEQ-T7

Ultra-high Throughput

Whole Genome Sequencing, Deep Exome Sequencing, Transcriptome Seqencing and Targeted Panel Projects

FC

1 lane

Ultra-high Throughput

6TB

5000M

24-30 hours for Pe 150 sequencing

PE100

PE150

DNBSEQ-G400

Adaptive

WGS, WES, Transcriptome sequencing etc.

FCL & FCS

2 or 4 lanes

High Throughput

1440GB

1500-1800M

FCS: 13-37 hours;
FC:: 14-109 hours

SE50

SE400/PE200

DNBSEQ-G400*
For HotMPS Only

Adaptive

WGS, WES, Transcriptome sequencing etc.

FCL

4 lanes

High Throughput

720GB

1500-1800M

15.5-50.5 hours

SE50

PE100

DNBSEQ-G50

Effective

Small whole genome sequencing, targeted DNA/RNA panels, low-pass whole genome sequencing

FCL & FCS

1 lane

Medium Throughput

150GB

500M / 100M

9-40 hours

SE50

PE150

https://en.mgi-tech.com/products/

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.

Opentrons

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Twist Bioscience

https://opentrons.com/

OT-2 LAB ROBOT

OT-2 WORKSTATIONS

OT-2 HARDWARE MODULES

CONSUMABLES & REAGENTS

VERIFIED LABWARE

SERVICE OFFERINGS

OT-2 Robot

OT-2 Pipettes

NGS Workstation

PCR Workstation

Temperature Module

Reagents

Reservoirs

Expedited Custom Protocols

Protein Purification.

Magnetic Module

Tubes & Vials

Tube Racks

12 Month Extended Warranty

Nucleic Acid Extraction

HEPA Module

NGS Library Prep

Thermocycler Module

Tips & Filter Tips

Lab Plates

Custom Protocols

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.

Genes

Oligo Pools

NGS

Variant Libraries

Synthetic Controls

Antibody Discovery

SARS-CoV-2 Tools

DNA Data Storage

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.

Clonal Genes

Genes Fragments

Genes

Library preparation

Synthetic Controls

SARS-CoV-2 Tools

Fixed Panels

Synthetic Controls

Antibody Discovery

Liquid Biopsy

Antibody Services

Catalog Antibodies

Infectious Disease

Reagents & Kits

Controls and Standarts

Controls and Standarts

NGS

Fixed Panels

Oligo Pools

Clonal Genes

Enzymatic Fragmentation Kit

cfDNA Pan-cancer
Reference Standards

SARS-CoV-2 NGS Assay-EUA

SARS-CoV-2 Research Panel

SARS-CoV-2 RNA Controls

Respiratory Virus Controls

Custom Panels

Exome 2.0

Gene Fragments

Universal Adapter System

SARS-CoV-2 Controls

Antibody Discovery

Partnership & Collaborations

Anti-ACE2

UMI Adapter System

Respiratory Virus Controls

Antibody Optimization

Pipeline & Licensing

Anti-SARS-CoV-2 S1

Fast Hybridization and Wash Kit

SARS-CoV-2 RNA Controls

Combinatorial Variant Library

Twist 96-Plex Library Prep Kit

High throughput antibody production

Standard Hybridization and Wash Kit

Respiratory Virus Controls

Spread Out Low Diversity Libraries

Universal Blockers

cfDNA Pan-cancer
Reference Standards

Site Saturation Libraries

Methylation Detection System

Alliance Panels

Human Comprehensive Exome

Human Core Exome

Mouse Exome Panel

SARS-CoV-2 NGS Assay-EUA

Human RefSeq Panel

Respiratory Virus Research Panel

Comprehensive Viral Research Panel

Mitochondrial Panel

SARS-CoV-2 Research Panel

Other Brands

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SWIFT bioscience

Isohelix

NEST

OPTOLANE

GeneMind

Other Brasnds

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.

Antibodies Incorporated

Assay Designs

Epichem

BioActs

Immundiagnostik

Cell Technology

RD-Biotech

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 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 laboratory.

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.

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