The Bionano Saphyr® system
Detects structural variations in an unbiased manner at much higher sensitivities than sequencingbased
technologies, down to 500 bp resolution and routinely at 5% variant allele fraction.
- Detect genome-wide SVs at >10,000x higher resolution over karyotyping
- Detect genome-wide CNVs and fusions, including fusion partners.
- Identify genes of interest, their locations, and how SVs impact them, for effective therapy development
- Detect somatic rearrangements in heterogeneous tumors at 5% variant allele fraction
- A workflow alternative to multiple traditional cytogenetic methods
Biomark X The new benchmark in genomics
Biomark™ X and a portfolio of integrated fluidic circuits (IFCs) and reagent kits facilitate a broad range of applications and throughput needs using real-time PCR
- Throughput from 120 to more than 1000 samples/day
- Validated Kits for nucleic acid extraction
- Flexible sample volume range from 10 µl to 10 ml
- User-friendly interface
C1 System lets you prepare single-cell templates for mRNA sequencing, DNA sequencing, epigenetics or miRNA expression.
C1 system carefully isolates single cells into individual reaction chambers in the exclusive Fluidigm integrated fluidic circuit (IFC).
- C1 automatically isolates up to 800 individual cells to separate reaction chambers.
- Labels each cell and microscopically images the IFC to confirm cell count, viability or phenotype.
- Lyses each cell for amplification.
- Amplifies each cell’s RNA or DNA content for sequencing or qPCR detection.
- All in as little as four hours
Innovative products for high throughput single cell research
Droplet Based scRNA-Seq methodology. Using droplet microfluidics, achieves unprecedented access to the transcriptomes of thousands of single cells.
- High throughput – 5,000 – 10,000 single cell transcriptomes per run
- High capture rate
- Fully automated sample encapsulation
- Processing capability of up to 8 samples in parallel.
- Easy-to-use
NEXTflex® library preparation kits
NEXTflex® library preparation kits are designed to reduce bias and increase the sensitivity, flexibility, and speed of library prep for both Illumina® and Ion Torrent™ sequencing platforms.
- DNA Sequencing Library Prep
- RNA Sequencing Library Prep
- Small RNA Sequencing Library Prep
- Metagenomics
- Epigenetics
- Amplicon Panels
LabChip GX Touch Nucleic Acid Analyzer
DNA and RNA quantitation and sizing can be done in seconds using automated capillary electrophoresis separation.
- NGS library preparation (smear and fragment analysis) and quality control
- RNA and DNA fragment analysis (including cell-free (cfDNA), FFPE, liquid biopsy, and PCR-free samples)
- Quantitation and qualification for CRISPR fragment analysis
- Agarose gel workflows