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GenoLab M High-throughput Sequencing Platform (Copy)

The high-throughput sequencing system GenoLab M adopts the surface restricted fluorescence sequencing technique (SURFseq) based on surface amplification to identify the optical signals of bases. Its sequencing-by-synthesis approach delivers speed, flexibility, high accuracy, and low-cost.

GenoLab M can be configured to run 1 flowcell alone or 2 flowcells simultaneously---enabling a scalable solution tailored to your specific research needs. With single or dual flowcell options, the system can be tuned to meet output needs ranging from 37Gb to 300Gb reads per run, supporting the broadest range of applications.

Application \ Sample FCM X1 FCM X2 or FCH X1 FCM X1+ FCHX1 FCHX2
250M 500M 750M 1000M
NIPT
>7 M unique reads/sample
(SE75)
32 64 96 128
PGT-A
> 4M reads/sample
(SE75)
48 96 144 192
WES
Panel Size:40Mb(PE150)
7Gb/sample
10 20 30 40
RNA-Seq
>10M reads/sample
24 48 72 96
Panel Detection
5Gb/sample
(SE75)
12 24 36 48
mNGS
>20M reads/sample
(SE75)
12 24 36 48

 

Flowcell Type Reads Read Length Output Quality Scores Run Time
FCM 250M SE75 18Gb >80%>Q30 ~13hrs
PE75 37Gb >80%>Q30 ~24hrs
PE150 75Gb >80%>Q30 ~43hrs
FCH 500M SE75 37Gb >80%>Q30 ~17hrs
PE75 75Gb >80%>Q30 ~30hrs
PE150 150Gb >80%>Q30 ~53hrs