We’ve combined sample prep and library prep into one easy-to-use product, simplifying the process to create sequence-ready samples. With on-bead fragmentation, no library quantification is needed, which saves you time and increases sequencing data …

The library preparation process involves converting a genomic DNA sample (or cDNA sample) into a library of fragments which can then be sequenced on an NGS instrument. Breakthrough technology in our library prep helps you get to answers in less time.

Step 2: Library preparation. The library preparation process involves converting a genomic DNA sample (or cDNA sample) into a library of fragments which can then be sequenced on an NGS instrument. Learn more about library prep

Illumina RNA Prep with Enrichment: Exceptionally fast tagmentation-based library prep enables deep insights into many transcripts of interest, including the RNA exome; Single hybridization step; No mechanical shearing needed; Benefit of panel modularity; Compatible with low quality / degraded / FFPE tissue; Respiratory virus detection with ...

The Illumina RNA library prep portfolio includes a range of solutions to support various applications and sample types. Illumina RNA library prep offers flexibility, scalability, and performance with a rapid, automation-friendly workflow option to prepare sequencing-ready libraries in a single day. The RNA library preparation products mentioned in

Library prep and array kit selector. Find the right sequencing library preparation kit or microarray for your needs. Filter by method, species, and more. Compare, share, and order kits.

Illumina library preparation portfolio offers technology advancements that enable quality, precision, and ease of use for both DNA and RNA sequencing. As the foundation of an end-to-end NGS workflow, these kits are specifically optimized for Illumina instruments and secondary analysis platforms. Illumina library prep protocols accommodate a range

TruSeq DNA PCR-Free provides simple, all-inclusive library preparation for whole-genome sequencing applications. Researchers can sequence a wide variety of organisms, from small genomes such as bacteria to human whole genomes.

This guide walks you through the range of automation tools available for NGS library prep and helps you find a solution tailored for your application, throughput, and budget needs. Learn about top considerations for building your automated library prep protocol.

Includes reagents for processing blood samples with the Illumina DNA Prep and Illumina DNA Prep with Enrichment. Purchase library prep, enrichment, enrichment probe panel, and index adapter reagents separately.