Genetics and sequencing

  • Alpina
  • Analytik Jena
  • Anbio Biotechnology
  • BioAir S.p.A.
  • BIOLABO S.A.S.
  • Bionano
  • B Medical Systems
  • Consarctic
  • Convergent Technologies
  • Cube DX
  • Cytek
  • DiaSys
  • Dirui Industrial
  • DNA Diagnostic
  • Don Whitley Scientific
  • Edan
  • GeneProof
  • Genolution
  • Helmer Scientific
  • ImmunoIVD
  • ingenetix
  • inno-train
  • Izon Science
  • MPW med.instruments
  • Pacific Biosciences
  • QuantraMatrix
  • Sener
  • Siemens Healthineers
  • TRUPCR

The study of genetic information has become a key area of ​​active development in the scientific community, clinical practice, and the pharmaceutical industry. Today, a sequencer allows us to obtain detailed data on DNA structure, identify mutations, conduct complex genome analysis, and investigate various genetic characteristics of an organism. Technological advances have significantly expanded the capabilities of medicine, molecular biology, and genetics.

 

What is a DNA sequencer?

 

DNA sequencing refers to a laboratory method for determining the nucleotide sequence of a DNA molecule. This task is accomplished using specialized equipment that automatically reads genetic information and converts it into digital data for subsequent analysis. Any genetic sequencer is a highly accurate device capable of sequencing various types of samples. The results obtained help analyze individual fragments of the genome, investigate hereditary changes, and identify the genetic causes of diseases. Today, NGS sequencing technology is considered one of the most in-demand technologies in scientific and clinical practice. This method is characterized by high productivity, allows for the simultaneous examination of a large number of DNA regions and ensures high accuracy of the results obtained.

 

Where is a DNA sequencer used?

 


In clinical practice, sequencing helps to identify mutations that affect the development of the disease, clarify the diagnosis, assess the patient’s current condition and select the most effective treatment. Thanks to this, medicine receives additional tools for working with oncological, hereditary and rare diseases. Sequencing is no less actively used in scientific research. Modern genetics uses this method to study the structure of the genome, search for new biomarkers and analyze processes that influence the development of various pathologies. NGS testing is also of great importance, as it allows you to examine a large number of samples in a short time. This approach increases the speed of research and helps to obtain more complete information about the genetic material.

 


In the Empirika online store you can order:

 

  • Revio Next Generation Sequencing System. PacBio's high-throughput Revio™ system is designed for large-scale DNA research and complex genomic projects. This equipment uses HiFi reads technology, which combines long read sequencing with exceptional data accuracy. The system supports full-fledged phased genome analysis, helps to study complex DNA regions that are difficult to analyze with other technologies, and also allows you to replace several separate studies with a single workflow. This method is especially in demand in large scientific centers where mass sequencing of human genomes is carried out. Among the main features of Revio™ are support for population studies, productivity of up to 2500 complete human genomes per year, up to 480 Gb HiFi reads per day and the ability to simultaneously work with four SMRT Cells. This makes the ngs platform suitable for laboratories that require high performance and stable data quality.
  • Vega, a next-generation benchtop sequencing system. The compact Vega™ system from PacBio represents a new generation of equipment for high-precision genetic analysis. The platform utilizes HiFi sequencing with read accuracy of up to 99.9%, enabling genome and transcriptome sequencing, as well as epigenetic changes, without sacrificing data quality. Vega™ is particularly suitable for laboratories requiring benchtop NGS sequencing. Despite its compact size, the system possesses the capabilities of larger platforms and enables efficient analysis of biological samples of various origins. The device supports the detection of SNVs, indels, structural alterations, methylation, and full-length RNA sequencing. The system also enables the study of alternative splicing and epigenetic analysis. Its high accuracy ensures reliable detection of even minimal changes in DNA structure. For professionals interested in the price of DNA sequencing, it is important to consider not only the initial equipment costs, but also its performance, automation capabilities, and the volume of research performed.

 

Our Empirika store catalog features systems from leading manufacturers that help with sequencing, DNA analysis, complex genetic analysis, and maintaining a high level of research. Our competitive prices, detailed catalog, professional consultations, and the option to purchase equipment with delivery in Kyiv and throughout Ukraine make Empirika a reliable partner for laboratories, research centers, and medical institutions.