The different index kit versions (v1 and v2) are not chemically different. The v2 kits were introduced to provide more index combinations. When Set A though Set D are combined, up to 384 unique index combinations are possible. The v1 and v2 index kits provide some of the same indexes. For a list of indexes included in each kit, see Contents & Storage.
If you plan to scale up to multiplex more than 96 samples, the v2 index kits are recommended.
The Nextera XT kit is recommended for small genomes, PCR amplicons greater than 300 bp, plasmids, microbial genomes, concatenated amplicons, and double-stranded cDNA.
For a list of indexes, see Contents & Storage.
The estimated time for 8 samples is approximately 90 minutes for the prep and 70 minutes for the bead based normalization (BBN). The estimated time for 96 samples is approximately 3 hours for the prep and 90 minutes for the BBN.
The Nextera XT kit introduces faster tagmentation, easy-to-use workflow, and optional bead-based normalization with only 1 ng of input DNA. In comparison, the Nextera DNA kit is optimized for larger genomes and uses 50 ng of input DNA with no bead-normalization reagents. The reagents provided in the Nextera DNA Library Prep Kit and the Nextera XT Library Prep Kit have been optimized for each workflow and are not interchangeable.
Certain sample types are more likely to contain potential inhibitors of enzymatic reactions. For a list of potential inhibitors, see Nextera XT Library Prep: Tips and Troubleshooting (Pub. No. 770-2015-015).
Illumina recommends using the Nextera XT Library Prep Kit for microbial genomes < 5 Mb. For larger genomes, use the Nextera DNA, TruSeq DNA PCR-Free, or TruSeq Nano DNA library prep kits.
Smaller amplicon inputs into Nextera XT preps typically yield smaller insert size ranges. To maximize recovery of smaller fragments out of the AMPureXP cleanup we recommend > 300 bp to ensure even coverage across the length of the DNA fragment. An expected drop off in sequencing coverage about 50 bp from each distal end of a fragment may be seen. This is because the tagmentation reaction cannot add an adapter right at the distal end of a fragment. For PCR amplicon sequencing this can be easily averted by simply designing your amplicons to be ~100 bases larger than the desired insert to be sequenced.
For amplicons greater than 500bp, Illumina recommends using a 0.6x AMPure XP cleanup (30 μl volume of beads). For amplicons less than 500bp, Illumina recommends using a 1.8x AMPure XP cleanup (90 μl volume of beads) to maximize yield.
To obtain higher quality sequencing data, Illumina recommends sequencing samples with high diversity and avoiding monotemplate stretches during sequencing. Low diversity can occur with pools of one or a few amplicons. Additionally, it is important to maintain color balance for each base of the read or index read being sequenced, otherwise sequencing could fail due to registration failure. Please refer to the MiSeq System User Guide (part # 15027617) for recommendations on low diversity libraries or the Nextera XT User Guide (part # 15031942) for information on low plexity pooling guidelines.
For recommended index combinations, see Nextera Low Plex Pooling Guidelines (Pub. No. 770-2011-044).
Illumina library prep protocols include many features designed to increase ease-of-use and reduce total hands-on time. Library normalization is the process of obtaining equal amounts of library from different samples before loading the libraries onto the flow cell. The Nextera XT kit includes reagents for bead-based normalization.
Use the following guidelines to determine which normalization method to perform: standard or bead-based. For more information, see Best Practices for Standard and Bead-Based Normalization in Nextera XT DNA Library Preparation Kits (Pub. No. 470-2016-007).
When creating a sample sheet in Illumina Experiment Manager (IEM), the software alerts you when improper combinations are used. Thus, creating your sample sheet before beginning library prep and pooling is highly recommended.
Excepting HiSeq 2500, IEM does not provide notification for color balance problems. For guidance, see Nextera Low Plex Pooling Guidelines (Pub. No. 770-2011-044).
Always pool samples with valid index combinations to avoid image registration failures. MyIllumina.com provides bulletins on library pooling, including pooling guidelines for the NextSeq and MiniSeq systems.
Completing Nextera XT library prep requires ordering the library prep kit and corresponding index kits: Nextera XT DNA Library Prep Kits (catalog # FC-131-1024, FC-131-1096) and corresponding Nextera XT Index Kits (catalog # FC-131-1001, FC-131-1002, FC-131-2001, FC-131-2002, FC-131-2003, FC-131-2004). The indexes are optimized for the Nextera XT DNA Library Prep Kits and are not interchangeable with the Nextera DNA Library Prep Kit. The index plate fixture (catalog # FC-130-1005) is not included in the library prep kits or index kits, and must also be purchased separately.
The Nextera XT protocol is optimized for 1 ng of input DNA total. Illumina strongly recommends quantifying the starting genomic material. Nextera XT library prep kits use an enzymatic DNA fragmentation step and thus can be more sensitive to DNA input compared to mechanical fragmentation methods. The ultimate success of the assay strongly depends on using an accurately quantified amount of input DNA library. Therefore, the correct quantitation of the DNA library is essential.
To obtain an accurate quantification of the DNA library, quantify the starting DNA library using a fluorometric-based method specific for duplex DNA, such as the Qubit dsDNA BR Assay system. Use 2 μl of each DNA sample with 198 μl of the Qubit working solution for sample quantification. Avoid methods that measure total nucleic acid content (eg, nanodrop or other UV absorbance methods) because common contaminants such as ssDNA, RNA, and oligos are not substrates for the Nextera XT assay.
Although most amplicons of interest will not likely be high GC-content, please note that coverage of high GC-content amplicons may be more variable as compared to other amplicons.
Yes, the Nextera XT DNA Library Prep Kit is compatible with any Illumina sequencing instrument. When sequencing on a HiSeq X or HiSeq 3000/4000 patterned flow cell, Nextera XT DNA libraries might perform with relatively lower %PF due to their longer fragment size. However, these instruments typically provide more data due to the higher output.
A TruSeq Dual Index Sequencing Primer Box PE (PE-121-1003) or TruSeq Dual Index Sequencing Primer Box SR (FC-121-1003) is needed to sequence Nextera XT libraries on a HiSeq 2500 using TruSeq v3 chemistry. Use the PE box with paired-end flow cells and the SR box with single-read flow cells. Other HiSeq 2500 chemistry and other systems do not require this additional box.
For most sequencing systems, 2–4 nM of final library is required to denature and dilute libraries in preparation for sequencing. For details, see the denature and dilute libraries guide for your instrument.
Illumina does not support, and strongly advises against, running libraries prepared with different library prep kits in the same lane of a flow cell. Running libraries prepared by different library prep kits in different lanes of the same flow cell or spiking in Illumina PhiX control library in the same lane as any user-prepared libraries is supported.
If different library types are run in different lanes, dual index recipes and the Dual Index Primer Box are required. The indexes for TruSeq HT and Nextera are unique and not shared.
For paired-end flow cells, dual indexing now requires 23 additional cycles of sequencing - eight cycles for the Index 1 (i7) Read, eight cycles for the Index 2 (i5) Read, plus seven non-imaging, chemistry-only cycles at the beginning of the Index 2 (i5) Read. For single-read flow cells, dual indexing only requires 16 additional cycles of sequencing - eight cycles for the Index 1 (i7) Read and eight cycles for the Index 2 (i5) Read.
The appropriate analysis tool depends on the application. MiSeq Reporter includes various analysis workflows, including amplicon, assembly, metagenomics, and resequencing. BaseSpace Sequence Hub also offers various apps for de novo assembly, metagenomics, resequencing, and so on.