– Large Whole-Genome Sequencing (human, plant, animal)
– Small Whole-Genome Sequencing (microbe, virus)
– Exome Sequencing
– Targeted Gene Sequencing (amplicon, gene panel)
– RNA sequencing
– Methylation sequencing
– Shotgun Metagenomics
illumina
Instrument
Scalable platform; Flexible performance & Streamlined operation
Model: NovaSeq 6000
Manufacturer: Illumina/USA
– Scalable platform
Match data output, time to results, and price per sample to study needs
– Flexible performance
Configure sequencing method, flow cell type, and read length to support a broad range of applications
– Streamlined operation
Increase lab efficiency with a simplified workflow and reduced hands-on time
– Large Whole-Genome Sequencing (human, plant, animal)
– Small Whole-Genome Sequencing (microbe, virus)
– Exome Sequencing
– Targeted Gene Sequencing (amplicon, gene panel)
– RNA sequencing
– Methylation sequencing
– Shotgun Metagenomics
Flow cell | |||||
SP | S1 | S2 | S4 | ||
Output data | 2 × 50 bp | 65–80 Gb | 134–167 Gb | 333–417 Gb | N/A |
2 × 100 bp | N/A | 266–333 Gb | 667–833 Gb | 1600–2000 Gb | |
2 × 150 bp | 200–250 Gb | 400–500 Gb | 1000–1250 Gb | 2400–3000 Gb | |
Quality of Q30
|
2 × 50 bp | ≥ 85% | |||
2 × 100 bp | ≥ 80% | ||||
2 × 150 bp | ≥ 75% | ||||
Running time | 2 × 50 bp | ~13 hr | ~13 hr | ~16 hr | N/A |
2 × 100 bp | N/A | ~19 hr | ~25 hr | ~36 hr | |
2 × 150 bp | ~25 hr | ~25 hr | ~36 hr | ~44 hr |
Details: https://sapac.illumina.com/systems/sequencing-platforms/novaseq.html
Supplier
Illumina
SOLIDaccuTest™ is an excellent tool for discovering variants associated with solid tumors using a comprehensive approach to next-generation sequencing (NGS). It reflects the latest research trends and is optimized for medical purposes by selecting essential genes of solid tumors including lung, colon, breast, skin brain, stomach and ovarian cancers, etc.
BRCAaccuTest™ PLUS with CE-IVD certificate for HBOC Breast/Ovarian Cancer Test
BRCAaccuTest™ & BRCAaccuTest™PLUS is a regent for producing libraries for
analyzing the BRCA ½ genes using the NGS (next-generation sequencing) method,
which analyzes genomic DNA derived from blood or FFPE tissues.
Model: NextSeq 1000
Manufacturer: Illumina
Origin: Singapore/United States
Launching year: 01/2020
PANARealTyperTM HPV Screening Kit is an in vitro diagnostic kit for the determination of the presence or absence of HPV virus (Human papilloma virus) using a peptide nucleic acid (PNA) probe.
DxFLEX is a new clinical flow cytometry platform derived from the successful CytoFLEX. The advanced sensitivity and intuitive software DxFLEX makes flow cytometry routine for both novice and expert flow cytometry technicians and promotes standardization. Functionality in the autoloader facilitates accurate results and sample tracking.
Model: NovaSeq 6000
Manufacturer: Illumina/USA
– Scalable platform
Match data output, time to results, and price per sample to study needs
– Flexible performance
Configure sequencing method, flow cell type, and read length to support a broad range of applications
– Streamlined operation
Increase lab efficiency with a simplified workflow and reduced hands-on time
TruSight Tumor 26 Kit includes library preparation reagent set and uses next-generation sequencing (NGS) technology to provide a comprehensive assessment of 26 genes that are commonly related to mutations in solid tumors and somatic variants
Developed with cancer genomics experts in collaboration, oligos ready-to-use, pre-engineered oligos allow researchers to sequence a wide range of genes and single nucleotide polymorphisms (SNPs) in advance. this is related to cancer predisposition
Model: Nextseq 550
Manufacturer: Illumina/USA
– Is the only sequencing system capable of deploying applications running sequencing and reading microarray biochips
– New generation DNA sequencing system using synthetic sequencing technology: Sequencing by Synthesis – SBS
– The whole process of gene sequencing is conducted on the surface of flow cells, convenient to use and easy to manipulate.