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xGen™ for Ultima Genomics®

Trusted IDT xGen NGS chemistries for emerging sequencers

Whether your project requires a basic indexing solution or a more sophisticated design for higher accuracy, we have the products and expertise to deliver the right solution for Ultima Genomics platforms.

xGen NGS—made platform-agnostic

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  • IDT is a leading provider of high-purity ligation-based and PCR-indexing solutions for NGS, and now we are proud to offer adapters and indexing primers for sequencing on Ultima Genomics systems
  • xGen for Ultima products are available to support both whole genome sequencing (WGS) and targeted sequencing (via hybridization capture) workflows
  • Barcodes are designed with edit distance in mind to minimize any sequence errors from PCR or sequencing that might impact demultiplexing
  • IDT is the first to offer stocked Universal Blocking Oligos for the Ultima system—designed specifically for their native adapters

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xGen™ for Ultima Genomics® 

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Product details

IDT has several solutions available for customers sequencing on an Ultima Genomics platform—the best solution for you depends on your workflow. Please refer to Table 1 for adapter and indexing primer recommendations based on library prep method and the WGS/target enrichment workflow information tabs for guidance specific to your whole genome sequencing or hybridization capture workflow needs.

Table 1. Recommended xGen for Ultima adapters and indexing primers based on compatibility with library prep methods.

PCR-Free AdaptersHybCap Adapters* Indexing Primers
xGen Broad-range RNA Library Prep Kit   
xGen RNA Library Prep Kit   
 
xGen DNA Library Prep (MC or EZ) Kit   
xGen DNA Library Prep (MC or EZ) UNI Kit  
 
xGen ssDNA & Low-input DNA Library Prep Kit   
 
xGen Methyl-Seq Library Prep Kit   
 
xGen cfDNA & FFPE DNA Library Prep Kit   

* Only the HybCap adapters may be used for construction of libraries intended for hybridization capture target enrichment
† Amplification must be done using a uracil-tolerant polymerase. IDT recommends the UG Amplification kit (catalog # 20020007), available from Ultima Genomics

Whole genome sequencing (WGS) workflow

We offer xGen for Ultima solutions for both PCR-free and PCR-dependent WGS workflows, each with flexible options depending on the number of samples.

  • xGen PCR-Free Adapters for Ultima Genomics
    • For applications with adequate gDNA input to support a PCR-free workflow, or when indexing by ligation is preferred
  • xGen Indexing Primers for Ultima Genomics
    • For applications where indexing by PCR is preferred
    • Requires uracil-tolerant PCR mix, found in the UG Amplification Kit available from Ultima Genomics (catalog # 20020007)
    • xGen Stubby Adapter (catalog # 10005974 or 10005924, sold separately) may be required; refer to Table 1 and Figure 1 for details

All xGen sample indexing products for Ultima are loaded into single-use 96-well plates containing a pierceable seal. The sample barcode has a length of either 15 or 17 nucleotides—consult the index list and plate map for further details. Each well contains material for indexing one sample.

Sample multiplexing:

  • For an 8-plex, use any column

Please contact us with any questions.

Figure 1. xGen for Ultima Genomics WGS workflow

Target enrichment workflow

Confidently perform target enrichment via hybridization capture with the following xGen for Ultima HybCap products: 

  • xGen HybCap Adapters for Ultima Genomics
    • Used for library construction prior to hybridization capture
    • Requires conditioning with the Ultima Genomics UG Library Amplification Kit prior to sequencing*
  • xGen HybCap Lib Amp Primers for Ultima Genomics
    • Designed to increase yield for sequencing post-hybridization capture
  • xGen Universal Blockers for Ultima Genomics
    • Reduces non-specific adapter interaction during hybridization

* Different adapters are required for hybridization capture due to the modifications found on the native Ultima adapters. Due to this, after hybridization capture, conditioning of the final library using the UG Amplification Kit available from Ultima Genomics (catalog # 20020007) is required prior to sequencing on the Ultima platform.

All xGen sample indexing products for Ultima are loaded into single-use 96-well plates containing a pierceable seal. The sample barcode has a length of either 15 or 17 nucleotides—consult the index list and plate map for further details. Note that there is no difference in the index sequences between products used for WGS or target enrichment. Each well contains material for indexing one sample. The xGen Universal Blockers and HybCap Lib Amp Primers for Ultima are both delivered in multi-use tubes.

Sample multiplexing:

  • For an 8-plex, use any column

Please contact us with any questions.

Figure 2. xGen™ for Ultima Genomics® Targeted (Hybridization Capture) Sequencing Workflow.

Table 2. Product specifications 

Indexing optionxGen PCR-Free Adapters for Ultima GenomicsxGen Indexing Primers for Ultima GenomicsxGen HybCap Adapters for Ultima Genomics
Sample index length15 or 17 nucleotide indexes15 or 17 nucleotide indexes15 or 17 nucleotide indexes
Concentration

15 µM total,
7.5 µM (each adapter)

20 µM total,
10 µM (each primer)

15 µM total,
7.5 µM (each adapter)

Shipping container96-well plates, single use96-well plates, single use96-well plates, single use
Reactions1 reaction per adapter1 reaction per primer pair1 reaction per adapter
Platform compatibilityUG 100™UG 100UG 100

 

Product data

Methyl-seq library preparation workflow comparisons

The xGen Methyl-Seq DNA Library Prep Kit has a post-bisulfite library preparation workflow to maximize library complexity by converting bisulfite-induced single-stranded fragments directly into library molecules. Traditional methods construct libraries from dsDNA using methylated adapters followed by bisulfite conversion that leads to significant library loss due to bisulfite-induced DNA fragmentation. The random priming methods are also post-bisulfite but have reduced library complexity due to a lower efficiency biased workflow (see Table 2; Figure 3).

Frequently asked questions

References

  1. Jones PA. Functions of DNA methylation: islands, start sites, gene bodies and beyond. Nat Rev Genet. 2012 May 29;13(7):484-92. doi: 10.1038/nrg3230. PMID: 22641018.
  2. Luo C, Keown CL, Kurihara L, et al. Single-cell methylomes identify neuronal subtypes and regulatory elements in mammalian cortex. Science (New York, NY). 2017;357(6351):600-604.
  3. Luo C, Rivkin A, Zhou J, et al. Robust single-cell DNA methylome profiling with snmC-seq2. Nat Commun. 2018;9(1):3824.
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