User Guides
AVITI System User Guide (MA-00008)
Getting Started with Elembio Cloud
Software Release Notes
AVITI™ OS 2.6.0, 2.6.1, and 2.6.2 Release Notes
AVITI OS v2.5.1 and v2.5.0 Release Notes
AVITI OS v2.4.1 and v2.4.0 Release Notes
AVITI OS v2.3.0 Release Notes
AVITI OS v2.2.0 Release Notes
AVITI OS v2.1.0 Release Notes
AVITI OS v2.0.0 Release Notes
AVITI OS v1.1.0 Release Notes
AVITI OS v1.2.3 Release Notes
View more +
Site Prep Guides
AVITI System Site Prep Guide (MA-00007)
Quick Start Guides
Cloudbreak Sequencing Quick Guide (MA-00009 Rev L)
Other
Bases2Fastq Download
Knowledge Base Articles
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?
Changing Settings with Bases2Fastq
How often should I run the maintenance wash?
Can I use regular bleach in the maintenance wash?
When would I use the --legacy-fastq‚ bases2fastq option?
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?
When should I use the Low-Diversity High-Multiplex setting?
View more +
Software Documentation
Remote run monitoring
Provider integrations
Storage connections
Integrate Amazon Web Services
Integrate Google Cloud Platform
ElemBio Catalyst Documentation
