illumina nextera dna
Note that sequencing nextera xt libraries on certain instruments the hiseq 1000 2000 hiseq 1500 2500 in. The low amount 1 ng of input dna makes this method amenable to precious samples available in limited quantity. Therefore only 50 ng was used in this experiment.
Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research translational and consumer genomics and molecular diagnostics.

Illumina nextera dna. The fast and simple protocol allows for treatment of one or a pool of libraries just prior to sequencing on any illumina platform. Nextera xt dna library prep kit protocol. Of the miseq system and nextera xt dna library preparation kits enable you to go from dna to data in 8 hours figure 1. The illumina free adapter blocking reagent is an optional reagent that can be used to treat most types of sequencing libraries to reduce index hopping levels.
Illumina recommends 50 ng input for nextera and not an input range. For each sample we used both the product of the cl reaction and the rca reaction for library preparation using the nextera dna library preparation kit illumina with a modified protocol to. Compatible with all illumina sequencers nextera library preparation can shorten the. Nextera dna flex documentation.
Find the right kit. With this series of protocols and the opentrons magnetic module your robot can complete a library prep using the illumina nextera xt dna library prep kit this library prep protocol comes in four parts. 20025519 20025520 20018704 and 20018705. Tagment and amplify clean up libraries normalize libraries and.
Tagment genomic dna nexteradnalibraryprepreferenceguide 9 tagmentgenomicdna thisstepusesthenexteratranspsometotagmentgdna whichisaprocessthat. Part 1 4 tagment genomic dna and amplify libraries. For research use only. The products previously known as nextera dna flex library prep are now called illumina dna prep cat.
These products use the same tagmentation technology as the previous nextera flex kits. A high performing fast and integrated workflow for sensitive applications such as human whole genome sequencing. Library prep kit selector. Not for use in diagnostic procedures except as specifically noted.









































































