Simple, all-inclusive prep solution, ideal for whole-genome sequencing. This new workflow offers reduced DNA input allowing for interrogation of samples with limited available DNA while providing excellent genomic coverage and uniformity. The LT option is available in Set A and Set B. Each set contains 12 unique single indexes that can be pooled together for up to 24plex.
Simple, all-inclusive prep solution, ideal for whole-genome sequencing. This new workflow offers reduced DNA input allowing for interrogation of samples with limited available DNA while providing excellent genomic coverage and uniformity. The HT option provides dual index combinations for up to 96plex.
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Species Compatibility | Compatible with most large DNA genomes | ||||||
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Recommended Illumina Instrument* | NextSeq 500 | HiSeq 2500 (Dual Flow Cell) | NovaSeq 6000 (Dual Flow Cell) | ||||
Recommended Samples per run† | 1 | 2–10 | 8 | 16 | 48 | ||
Run Mode | Mid Output | High Output | Rapid Run | High Output | S1‡ | S2 | S4 |
Max Recommended Read Length | 350 bp insert: ≤ 2×101 bp 550 bp insert: ≤ 2×151 bp |
350 bp insert: ≤ 2×101 bp 550 bp insert: ≤ 2×151 bp |
350 bp insert: ≤ 2x101 bp 550 bp insert: ≤ 2x151 bp |
350 bp insert: ≤ 2x101 bp 550 bp insert: ≤ 2x126 bp |
350 bp insert: ≤ 2×150 bp 550 bp insert: ≤ 2×150 bp |
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Recommended Secondary Analysis |
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Recommended Down Stream Analysis | VariantStudio |
* Library prep is compatible with all Illumina instruments. Recommended instruments chosen based on typical output and analysis need for selected application.
† Based on 30x coverage of a human genome.
‡ NovaSeq S1 Reagent Kits are not currently available.