User Guides
ElemBio Catalyst Documentation
AVITI24 System User Guide (MA-00051)
Getting Started with Elembio Cloud
Teton CytoProfiling User Guide (MA-00053 Rev F)
Technical Notes
Teton™ Protein Performance on AVITI24™ Tech Note (LT-00068 Rev A)
Software Release Notes
AVITI OS 3.0.0, 3.1.0 Release Notes
Site Prep Guides
AVITI24 System Site Prep Guide (MA-00052)
Other
1-Well Cytoprofiling Run Manifest Template
12-Well Cytoprofiling Run Manifest Template
Software Documentation
Introduction
Overview
Share or update a canvas
Remote run monitoring
Provider integrations
Storage connections
Integrate Amazon Web Services
Integrate Google Cloud Platform
Integrate your Seqera account
AI Tooling
View more +
Knowledge Base Articles
Drying Teton Slides Prior to Flow Cell Assembly
Surface Recommendations for iPSC-derived Mesenchymal Stem Cells (MSC) and Neural Progenitor Cells (NPC)
How should I prepare my libraries for Cloudbreak UltraQ Sequencing?
Are HPLC-purified indexing primers required for library preparation when using Cloudbreak Freestyle for sequencing?
How much library should I load with AVITI24 to maximize output?
Are Elevate, Adept, and Freestyle 3rd Party PhiX interchangeable?
Optimization and Culture Techniques for Suspension and Adherent Cells
Disassembling the Teton Slide Kit using the Teton Slide Kit Tool
Optimizing Matrigel Surface Coatings for Teton CytoProfiling Runs
Cell Culture Recommendations for 48-well Teton Slide Kits
Guidance for assembling a flow cell using the Teton Flow Cell Aligner and Sealer
When should I enable Expert Mode HD for my sequencing run?
How does increased sequencing output on AVITI24‚Ñ¢ compare to performance on AVITI with and without Expert Mode HD?
Will I still experience output improvements on AVITI24 without increasing library loading concentration?
How should I prepare my long insert libraries for Cloudbreak Freestyle Sequencing?
Can I use custom primers on the AVITI?
What are some best practices for library quantification and loading to maximize my sequencing run density?
Guidance for discarding a run setup after a flow cell is loaded and instrument priming is complete
How do I change my Trinity hybridization conditions with a custom panel?
What are pass-filter reads and how do I calculate pass-filter rate?
Can I set up a run without a run manifest?
How should I adjust my hybridization program for an AT-Rich panel with Trinity Freestyle?
Assessing Your Cloudbreak and Cloudbreak Freestyle Sequencing Runs
How can library pools with samples of varying index lengths be sequenced on the AVITI and demultiplexed in Bases2Fastq?
Does the QIAseq miRNA Library Kit require a custom sequencing primer on AVITI?
Can libraries that have undergone Adept conversion be sequenced with Cloudbreak Freestyle sequencing reagent kits?
Where can I find SDS?
Where can I see examples of underloaded and overloaded thumbnail images?
Which sequencing recipe should I use for my library insert size?
Can I use asymmetric read length conditions on a run, i.e. 200+100 for a 300 cycle kit?
What is the maximum allowable index length?
Can we run different types of libraries on the flow cell lanes?
Do we have any recommendations for profiling peripheral blood mononuclear cells (PBMCs) with Teton‚Ñ¢?
How often should I run the maintenance wash?
Can I use regular bleach in the maintenance wash?
Data from how many runs are stored on the AVITI instrument?
How often should the AVITI be power cycled?
Do I need to wash the instrument after every run?
The user guide recommends index lengths < 32 bp, can I go above this?