Magnis NGS Prep System
RUO
The Magnis system provides a complete workflow for NGS library preparation that is fully automated and delivers reproducible results. Built on proven Agilent SureSelect XT HS2 chemistry, start from total RNA with integrated cDNA conversion or unfragmented DNA with onboard enzymatic fragmentation for increased workflow efficiency.
This new bench-top instrument self-detects and tunes; the reagents come pre-aliquoted; and pre-set protocols are included.
The?system requires minimal expertise to run. The onboard wizard allows assays to be set up in under five?minutes. In addition, the?Magnis?notifies users of correct reagent placement through automated barcode checking. Upon pressing the start button, the user can walk away from the?instrument, yet visually check progress through the wizard and the LED status indicator.??
This new bench-top instrument self-detects and tunes; the reagents come pre-aliquoted; and pre-set protocols are included.
The?system requires minimal expertise to run. The onboard wizard allows assays to be set up in under five?minutes. In addition, the?Magnis?notifies users of correct reagent placement through automated barcode checking. Upon pressing the start button, the user can walk away from the?instrument, yet visually check progress through the wizard and the LED status indicator.??
For Research Use Only. Not for use in diagnostic procedures.
- NGS Automation Platforms
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This product is not available for purchase by the general public.
Product Details
Features
- Magnis works seamlessly with Agilent’s industry-leading SureSelect target enrichment system and delivers sequencing data?that are?robust,?traceable,?and reproducible
- This benchtop instrument self-detects and tunes; the reagents are provided pre-aliquoted; and the system comes with pre-set protocols for Agilent’s catalog and custom assays.
- The LED status indicator will light up green allowing you to monitor status easily from a distance.
- When combined with the Agilent 4150?TapeStation System, the Magnis system?provides quality control of the sample throughout the workflow.
Specifications
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Literature
- Key Literature
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Walkaway NGS Automation With Magnis NGS Prep System
The Agilent Magnis NGS prep system is a compact, benchtop platform providing an automated, completely walkaway next-generation sequencing (NGS) library preparation and target enrichment solution.- Flyers
- English
- 11 Sep 2023
- 904.48 KB
- Application Notes
- Brochures
- Data Sheets
- Flyers
- Posters
Support
- User Manuals
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Magnis/MagnisDx NGS Prep System, Quick Reference Guide, English
Quick Reference Guide for the Magnis/MagnisDx NGS Prep System- User Manuals
- English
- 03 Jun 2024
- 495.17 KB
Magnis/MagnisDx NGS Prep System, User Guide, English
User Guide for the Magnis and MagnisDx NGS Prep Systems- User Manuals
- English
- 03 Jun 2024
- 3.54 MB
Magnis/MagnisDx NGS Prep System, Quick Reference Guide, Spanish
Quick Reference Guide for the Magnis/MagnisDx NGS Prep System- User Manuals
- Spanish
- 03 Jun 2024
- 476.27 KB
Magnis/MagnisDx NGS Prep System, User Guide, Spanish
User Guide for the Magnis and MagnisDx NGS Prep Systems- User Manuals
- Spanish
- 03 Jun 2024
- 3.29 MB
Featured References
- Publications
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- Martinez-Gutierrez, L. N.; Burgher, B. C.; Glynias, M. J.; Alvarado, D.; Griffiths, E. A.; Glenn, S. T.; Sung, P. J. Evaluation of Hypereosinophilia in a Case of FLT3-Mutant Acute Myeloid Leukemia Treated with Gilteritinib. Molecular Case Studies 2023, 9 (3), a006279.
- Callens, C.; Rodrigues, M.; Briaux, A.; Frouin, E.; Eeckhoutte, A.; Pujade-Lauraine, E.; Renault, V.; Stoppa-Lyonnet, D.; Bieche, I.; Bataillon, G.; Karayan-Tapon, L.; Rochelle, T.; Heitz, F.; Cecere, S. C.; Pérez, M. J. R.; Grimm, C.; N?ttrup, T. J.; Colombo, N.; Vergote, I.; Yonemori, K. Shallow Whole Genome Sequencing Approach to Detect Homologous Recombination Deficiency in the PAOLA-1/ENGOT-OV25 Phase-III Trial. Oncogene 2023, 42 (48), 3556–3563.
- Gargallo, P.; Molero, M.; Bilbao, C.; Stuckey, R.; Carrillo‐Cruz, E.; Hermosín, L.; Pérez‐López, O.; Jiménez-Velasco, A.; Soria, E.; Marián Lázaro; Carbonell, P.; Yania Yá?ez; Isabel Neira Gómez; Izquierdo-García, M.; Valero-García, J.; Carlos Alberto Ruíz; Such, E.; Calabria, I. Next-Generation DNA Sequencing-Based Gene Panel for Diagnosis and Genetic Risk Stratification in Onco-Hematology. Cancers 2022, 14 (8), 1986–1986.
- Emiliani, F.; Aziz, A.; Hughes, E.; Tsongalis, G.; Zanazzi, G.; Lin, C.-C. ISCORED: Nanopore-Based Random Genomic Sampling for Intraoperative Molecular Diagnosis. medRxiv (Cold Spring Harbor Laboratory) 2023.
- Martinez-Gutierrez, L. N.; Burgher, B. C.; Glynias, M. J.; Alvarado, D.; Griffiths, E. A.; Glenn, S. T.; Sung, P. J. Evaluation of Hypereosinophilia in a Case of FLT3-Mutant Acute Myeloid Leukemia Treated with Gilteritinib. Molecular Case Studies 2023, 9 (3), a006279.
Tools
Reduce your hands-on library preparation and target enrichment time with the Magnis NGS Prep System.
Videos
News
Magnis Receives The LSIA 2109 Industry Silver Award
- 30 Jan 2020
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