for LifeScience solutions
for LifeScience solutions
extraction
Library Preparation
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.
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
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
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.
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