Illumina DNA PCR-Free Prep, Tagmentation
- Whole Genome Sequencing
- Delivers consistent insert sizes, uniform coverage, and optimized performance
- Bead-based technology minimizes bias and opportunities for error
- PCR-free workflow avoids PCR duplicates
- On-bead fragmentation
- No library quantification needed
- Very quick turn-around time
- How it works
- Suitable for:
- Human DNA WGS
- Multiple sample types
- Small and large genomes
- Recommended replacement for the TruSeq DNA PCR-Free kit
- Required DNA input (in a volume ≤ 25 μL):
- 25 - 2000 ng
- Includes:
- 10 bp unique dual indexes (Illumina DNA/RNA UD Indexes, Tagmentation)
- Multiplexing of up to 384 samples
Illumina DNA Prep, (M) Tagmentation
- Previously called the Nextera DNA Flex kit
- Whole Genome Sequencing
- Delivers consistent insert sizes (~350 bp), uniform coverage, and optimized performance
- Bead-based technology minimizes bias and opportunities for error
- PCR-based workflow
- On-bead fragmentation
- No library quantification needed
- Quick turn-around time
- Suitable for:
- DNA WGS with low input
- Multiple sample types
- Flexibility to sequence human or other large, complex genomes as well as amplicons or microbial species
- Recommended replacement for the Nextera DNA Library Prep kit
- Required DNA input (in a volume ≤ 30 μL):
- 1 - 500 ng
- Includes:
- 10 bp unique dual indexes (IDT for Illumina Nextera DNA UD Indexes)
- Multiplexing of up to 384 samples (using unique dual indexes)
NEBNext Ultra II DNA / NEBNext Ultra II FS DNA
- Higher library yields from lower input amounts
- Generates high yields with increased reaction efficiencies and minimized sample loss
- Reliable fragmentation with a single protocol, regardless of DNA input amount or GC content (optional)
- PCR-based workflow
- Tunable bead-based size selection to select for insert sizes ranging from 150 to 700 bp
- Quick turn-around time
- Suitable for:
- DNA with ultra-low input
- Multiple sample types including GC-rich and FFPE
- Genomic DNA, fragmented DNA, or amplicons
- Required DNA input:
- 0.5 - 1000 ng (in a volume ≤ 50 μL, without fragmentation)
- 0.1 - 500 ng (in a volume ≤ 26 μL, with fragmentation)
- Includes:
- Fragmentation (optional), end repair, dA-tailing, adapter ligation, PCR and index incorporation
- 8 bp unique dual indexes (NEBNext Multiplex Oligos for Illumina - UDI Primer Pairs)
- Multiplexing of up to 384 samples (using unique dual indexes)
Other Library Preparation Options
- Requests for projects requiring significant modifications to existing protocols or library preparation options not already listed here will be discussed with the customer on a per-project basis.