Strategic Alliances

• Sequencing by synthesis (SBS) responsible for more than 90% of the world's sequencing data*
• Efficient and scalable benchtop and production scale next-generation sequencers

• Enable diverse sequencing methods for a variety of sample types and throughput needs
• Focus areas include genomic research, cancer research, reproductive health, agrigenomics, complex disease, microbial genomics, and genetic health

*Data calculations on file. Illumina, Inc. 2015.

• Accurate quantification and qualification of RNA and DNA samples
• Illumina tested quality metrics to guide library preparation from challenging samples
• Superior sensitivity for low molecular weight fragments and contaminants
• Improved sizing of Illumina library smears
• Scalable throughput for parallel analysis of 12, 48, or 96 samples

• Learn more about the partnership.
• Illumina Streamlines Nucleic Acid Quality Analysis
• Scalable Nucleic Acid Quality Assessments for Illumina Next-Generation Sequencing Library Prep

• Deliver about ~7X more reads with 1 million zero-mode waveguides
• Ideal for generating whole genome de novo assemblies and for targeted enrichment studies
• Generate long reads with uniform coverage and high accuracy

• Reduce overnight QC steps to 1 hour
• Accurately size DNA fragments up to 50 kb
• Conserve sample for sequencing with minimal input requirement

PacBio Workflow Solution

• Separate, size, and quantify DNA smears through 165 Kb
• Requires only picogram quantities of DNA
• Complete separations in about 1.5 hours

Fast High-Res DNA Sizing

Best Practices for WGS

• Learn more about the partnership.
• Pacific Biosciences and AATI Announce Co-Marketing Agreement
• Genomeweb: Pacific Biosciences, Advanced Analytical Technologies Ink Comarketing Partnership

• High-quality fragmentation for long-read sequencing
• Automated walk-away processing
• Shear DNA from 3Kb to 75Kb
• Achieve tight fragment distributions

• Separate and size large fragment smears accurately
• Eliminate overnight PFGE separations
• Dramatically reduce library preparation time

Nature Methods Paper

Best Workflow Practices for ChIP-seq Analysis with Small Samples

• Accurately normalize samples based on molarity
• Automate important QC checkpoints
• Integrated software for remotely control operations

• All 5 drawers can interface with a robotic arm
• Robust API for continuous operation
• High resolution separation of 96 samples in parallel

Tecan Application Note

• Validated protocols for miniaturized molecular biology and genomics applications. Versatile, open system with intuitive software
• Precise and accurate low volume pipetting
• Ideal for reducing reagent consumption or handling precious sample

• Accurate quantification and qualification of large-scale scRNA-Seq preparations
• High throughput and efficient nucleic acid QC
• High detection sensitivity and broad sizing range with kits available for numerous applications

Mosquito / Fragment Analyzer Flyer

• AATI and TTP Labtech Alliance Delivers High-Throughput NGS Library Prep Solutions
• Genomeweb: Advanced Analytical, TTP Labtech Ink Comarketing Agreement for NGS Library Prep

• Reduce dead volumes to 6 µL
• Maximize reproducibility of library preps with precision down to 100 nL
• Miniaturize reactions to increase throughput without increasing costs
• Construct high-quality libraries, even from single cells

• Accurately quantify and qualify single cell library preparations
• High sensitivity nucleic acid detection and quantification with a broad sizing range for numerous applications
• Variable throughput enables the parallel analysis of 12, 48, or 96 samples