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Material # 20004364
Document # 15065681 v01
Introduction
Clustering with sample tracking is possible for all HiSeq flow cells except TruSeq Rapid
(v1). All clustering steps are performed on the cBot except preparing libraries for
sequencing and preparing reagents. Clustering steps for a HiSeq Rapid v2 flow cell consist
only of template hybridization and first extension. The remaining steps are performed on
the HiSeq.
Setting up the cBot for cluster generation with sample tracking includes steps to load run
components, select a protocol, and scan consumables. Internal scanners record required
input, such as reagent ID and flow cell ID, after consumables are loaded and the
instrument lid is closed. Manual input and system input are shown on the screen, if
necessary.
For information on configuring your cBot for sample tracking, see the
cBot System
Configuration Guide (part # 1000000005301)
.
Library Prep
Before setting up the cBot for cluster generation, prepare libraries for sequencing. The
process differs depending on library type and flow cell type.
}
Most libraries on TruSeq flow cells and HiSeq flow cells require a denaturation and
dilution step. For more information, see
HiSeq and GAIIx Systems Denature and Dilute
Libraries Guide (document # 15050107)
.
}
The denaturation protocol differs for HiSeq X and HiSeq 3000/4000 patterned flow cells.
Denature libraries for use with these flow cell types
only
as described in the reagent
preparation instructions for your flow cell type. For more information, see
Содержание cBot
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