GenoLab M High-Throughput Sequencing System GeneMind

GeneMind
#genolab-m

GenoLab M is a scalable sequencing system for laboratories that need flexible output without rebuilding their library preparation approach. The platform uses SURFseq sequencing-by-synthesis chemistry and can operate one flow cell independently or two flow cells simultaneously.

Key advantages

  • Single or dual flow cell operation for adjustable output
  • 37-300 Gb per run output range across listed configurations
  • Libraries can be used directly after preparation
  • Compatible with mainstream NGS libraries
  • Designed for applications including NIPT, PGT-A, WES, RNA-seq and mNGS

Availability may vary by country; confirm regional ordering status before purchase.

Type: Sequencing system

Section: Sequencers

lwh: 1170x690x600 mm

Weight: 200000 g

Product Advantages
Specification
Run Modes
Application Capacity

Product Advantages

AdvantageDetails
High IntegrationDNA template amplification and sequencing-by-synthesis reactions are integrated on the flow cell surface; prepared libraries can be used directly for sequencing.
High AccuracyReversible base termination chemistry with high-sensitivity fluorescence signal detection supports sequencing accuracy.
High CompatibilityCompatible with mainstream NGS libraries, reducing the need to redevelop sample preparation kits.

Specification

ParameterValue
TechnologySURFseq surface-restricted fluorescence sequencing
Flow cell optionsFCM, FCH
Output range37-300 Gb per run
Quality scoreQ30 > 85% for listed modes
Dimensions (L x W x H)1170 mm x 690 mm x 600 mm
Weight200 kg
Operating environment19-25 deg C; 20-80% RH, non-condensing; altitude below 300 m
Control computerWindows 10; Intel Xeon Silver 4216 2.1 GHz; 32 GB x 6 DDR4; 1 TB SSD; 10 TB HDD

Run Modes

Flow cellReadsRead lengthOutputQuality scoreRun time
FCM250MSE7518 GbQ30 > 85%~13 hr
FCM250MPE7537 GbQ30 > 85%~22 hr
FCM250MPE15075 GbQ30 > 85%~38 hr
FCH500MSE7537 GbQ30 > 85%~15 hr
FCH500MPE7575 GbQ30 > 85%~28 hr
FCH500MPE150150 GbQ30 > 85%~50 hr

Application Capacity

ApplicationData requirementFCM x1FCM x2 or FCH x1FCM x1 + FCH x1FCH x2
NIPT Standard>5M unique reads/sample, SE75326496128
PGT-A>3.5M unique reads/sample, SE75326496128
WES40 Mb panel, 10 Gb/sample, PE1506121824
RNA-seq>10M reads/sample24487296
Obesity detection1 Gb/sample, SE7518365472
mNGS>20M reads/sample, SE7512243648