Targeted DNA Seq
Achieve economy of scale with ease
Reduce hands-on time and drive down reagent consumption with automated microfluidics, resulting in significant savings. And to ensure that your NGS panel always remains up-to-date, maintain flexible customization capabilities unique to Fluidigm.
DATA SHEET | Juno Targeted DNA Sequencing Library Preparation System
Customized assay panels in convenient kits provide investigators and genomics service providers with an easily scalable and automated solution. Targeted DNA Sequencing Library Preparation is compatible with Illumina® MiniSeq™, MiSeq™, NextSeq™ and HiSeq® NGS systems.
FEATURE | Advanta CFTR NGS Library Prep Assay saves time and money through an efficient and scalable targeted NGS workflow
The Advanta™ CFTR NGS Library Prep Assay automates targeted enrichment of cystic fibrosis transmembrane conductance regulator (CFTR) variants from each of the gene’s 27 exons and select intronic regions using proven microfluidics technology. The workflow significantly lowers hands-on time while conserving precious reagents by reducing reactions to the nanoliter scale. With the capacity to produce from 48 to over 1,500 NGS libraries per week, scalability is simplified to meet laboratory needs as they change over time. Protocols are available that support Juno™ and Access Array™ systems.
Advanta Evidence-Based CFTR Variant Coverage Flyer DOWNLOAD
Juno Targeted DNA Sequencing Library Preparation
Scale with the industry’s most flexible per-sample throughput and enrichment capabilities using the Juno targeted DNA Sequencing Library Preparation System. Two sample throughput options are available, LP 48.48 and Juno LP 192.24 IFC (integrated fluidic circuit).
The LP 192.24 IFC automates amplicon-based libraries for 192 unique DNA samples per run and up to 2,400 amplicon targets per sample. The LP 48.48 IFC accommodates up to 48 DNA samples per run and up to 4,800 amplicon targets per sample. Targeted DNA Sequencing Library Preparation is fully compatible with all Illumina® sequencing systems. Up to 1,536 sample libraries may be multiplexed per sequencing run.
Access Array Library Preparation
Access Array™ delivers specimen flexibility supporting sample types of DNA extracted from germline and FFPE somatic samples. Access Array automates targeted DNA library preparation for 48 unique DNA samples per run and up to 4,800 amplicon targets per sample using Targeted DNA Seq Library reagents, or up to 480 amplicon targets per sample using Access Array chemistry.
The system is compatible with multiple sequencing platforms including Illumina® sequencing systems and, for use with Access Array chemistry, Ion Torrent™.
Dr. Dexi Chen, PhD, MD
Scott Magness, PhD
Jo Vandesompele, PhD
Christophe Lancrin, PhD
Ansuman Satpathy, MD, PhD
Shyam Prabhakar, PhD
Simone Mayer, PhD
Kelly Nudelman, PhD
Shyam Prabhakar, PhD
Jonathan M. Irish, PhD
Dr. Luc Teyton, MD, PhD
Scientist Michael Stubbington, PhD
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