– 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
Match data output, time to results, and price per sample to study needs
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 Type | |||||
SP | S1 | S2 | S4 | ||
Sequencing Output | 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 Scores | 2 × 50 bp | ≥ 85% | |||
2 × 100 bp | ≥ 80% | ||||
2 × 150 bp | ≥ 75% | ||||
Run 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
– 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
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.
SOLIDaccuTest™ is an excellent tool to explorer variants associated with solid tumors using a comprehensive method of next-generation sequencing (NGS). It reflects the latest research trends and is optimized for the medical purpose by selecting essential genes of solid tumors including lung, colon, breast, skin brain, gastric, 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: 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
The NextSeq 2000 Sequencing System uses patterned flow cells similar to those that power the NovaSeq™ 6000 System. The result is a highly flexible and scalable benchtop system that offers the highest cluster density flow cell of any on-market NGS system to date, driving down the cost per gigabase (Gb) of the sequencing run.
Model: NextSeq 1000
Manufacturer: Illumina
Origin: Singapore/United States
Launching year: 01/2020
The PANA RealTyper™ HPV Screening Kit is a CE marked diagnostic device in accordance with the European Union in vitro Diagnostic Medical Device Directive 98/79/EC
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
TruSight Tumor 26 Kit include reagents to prepare for Library preparation samples, sequencing 26 genes relating to solid cancer, variant of soma in NGS – Next Generation Sequencing of Illumina