GenoLab M

• Introduction:
  GenoLab M by GeneMind is an advanced molecular diagnostics platform designed to perform high-throughput genetic analysis with a focus on precision and accuracy for clinical and research purposes.

• Technology:
  GenoLab M integrates cutting-edge next-generation sequencing (NGS) and microarray technology, offering robust data collection and real-time analysis for a wide range of genetic markers and mutations.

• Advantages:
  It provides fast turnaround times, high sensitivity, low error rates, and the ability to analyze complex genetic data with minimal sample requirements, making it cost-effective and reliable.

• Applications:
  GenoLab M is used in clinical diagnostics, personalized medicine, genetic screening, cancer research, and rare disease detection, enabling precise treatment planning and patient management.

• Impact:
  The platform drives advancements in personalized healthcare, offering actionable genetic insights that improve patient outcomes, streamline diagnostics, and foster innovations in therapeutic development.

FCM : 250 Million reads / Flow cell Output upto 75 GB

FCH : 500 Million reads / Flow cell Output upto 150 GB

SURFSeq 5000

• The SURFSeq 5000 is a high-throughput sequencing platform that leverages "Surface Enhanced Fluorescence" technology. This method uses a specialized surface to enhance the detection of fluorescent signals during DNA sequencing, allowing for faster and more accurate reading of nucleotide sequences.

• Technology:
  It utilizes a novel optical detection system combined with fluorescently labeled nucleotides and high-resolution imaging to read DNA fragments in real time. The platform's surface enhancement improves the signal intensity, providing better sensitivity and reduced error rates compared to traditional sequencing methods.

• Advantages:

  • Higher Sensitivity: The enhanced fluorescence system provides a stronger signal, increasing sequencing accuracy and throughput.

  • Faster Results: The technology enables faster sequencing with reduced cycle times, making it ideal for large-scale genomic projects.

  • Reduced Errors: The precision in detection minimizes sequencing errors, improving data quality.

• Applications:

  • Genomic Research:

  • Clinical Diagnostics:

  • Microbial and Environmental Sequencing:

• Impact:
  The SURFSeq 5000's advanced sequencing capabilities allow for more comprehensive genomic analysis at a reduced cost and faster turnaround time, supporting a wide range of biological and medical research applications.

FCM : 500 Million reads / Flow cell Output upto 150 GB

FCH : 2000 Million reads / Flow cell Output upto 600 GB

• Introduction:
  SURFSeq Q by GeneMind is an advanced sequencing platform designed for high-quality, rapid genomic analysis, specializing in both DNA and RNA sequencing for comprehensive research and clinical applications.

• Technology:
  It utilizes a unique sequencing technology that combines single-cell RNA sequencing with high-resolution genomic profiling, offering deep insights into gene expression and genetic variations with high throughput.

• Advantages:
  SURFSeq Q delivers exceptional precision, fast data processing, scalable throughput, and minimal sample requirements, providing cost-effective solutions for high-complexity genomic studies.

• Applications:
  The platform is applied in personalized medicine, cancer genomics, gene expression analysis, rare disease diagnostics, and biomarker discovery, enabling better-targeted treatments and therapies.

• Impact:
  SURFSeq Q enhances the speed and accuracy of genomic research, accelerating discoveries in healthcare, advancing precision medicine, and improving patient outcomes through targeted therapeutic strategies.

FCM : 11.7 Billion reads / Flow cell Output upto 3.5 TB

FCH : 23.3 Billion reads / Flow cell Output upto 7 TB

SURFSeq Q : -

MrLH 96 Dx : -

• MrLH-96 automated workstation is designed for the efficient automation of high-throughput acid extraction and NGS library preparation and laboratory liquid processing procedure.

• With the principle of Air replacement of MrLH 96 DX, the specially designed consumable stacking system is able to guarantee full automation with no manpower on site.

• The Inheco temperature-controlled oscillation accessories not only ensure the stability of the oscillation but also have the accuracy of temperature control within the range of 4~70°C, which perfectly matches the NGS hybridization capture process.

• The script design system can be used to explore multiple applications and customize the workflow design.

• Product advantages includes Highly automated less Manpower is needed, Easy to connect with LIMS system, Compatible with Inheco Temperature control Module.

• Applications Include : -

Genoscout EM:-

• The Automated Nucleic Acid Extractor (GenoScout EM) is a high-throughput, high-precision device designed for nucleic acid extraction.

• It is paired with pre-packaged extraction reagents based on superparamagnetic silica-coated magnetic beads, This enables the extraction and purification of nucleic acids from a variety of biological samples, including blood, tissue, cells, body fluids, bacteria and viruses.

• The system realizes the purification and enrichment of nucleic acid through the adsorption, transfer, and release of magnetic beads by magnetic rods.

• Characterized by rapid and user-friendly operation with a high level of automation, the system is widely applicable in the fields of molecular diagnostics and animal disease detection.

• The system is equipped with built-in UV sterilization and a HEPA fltration system to reduce the risk of contamination, and the shut-down time is customizable.