Confidence When Every Read Counts

Confidence in every read separates signal from noise. Missed exons, biased fragments, or uneven coverage can hide critical variants, transcripts, or methylation sites. Twist delivers integrated fragmentation-to-enrichment solutions that maintain consistency and clarity across your entire sequencing workflow

  • Focuses sequencing on key regions for meaningful depth.
  • Cuts excess sequencing and analysis to lower cost and data load.
  • Improves sensitivity for low allele frequency variants.
  • Supports tailored panels for specific pathways or research goals.

Why Target with Twist

Target enrichment workflows with Twist deliver scalable, low bias, and highly uniform coverage across large and complex genomic regions; enabling broader discovery, higher sensitivity, and greater flexibility than amplicon or array based methods.

  target enrichment

Twist Target Enrichment

NGS Method

amplicon

Amplicon Sequencing

NGS Method

product

Array-Based Analysis

NGS Method
Design Method Fully customizable panels Fixed amplicons; redesign requires new primers Fixed content; no new targets
Performance traits Uniform coverage, even in GC-rich regions Uneven due to PCR bias Limited to preset markers
Variant classes Detects SNVs, indels, CNVs, fusions, isoforms Good for small SNVs; poor for complex variants Only known variants
Throughput / Format Scales from small to million-probe panels Hard to scale large panels Must buy new arrays for expansion
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How it works

Target Enrichment Sequencing Workflow

Target enrichment selectively captures the regions that matter; genes, exons, splice sites, or CpG islands; focusing sequencing power for deeper coverage, fewer wasted reads, and faster results.

Why choose us

Complete your Target

Enrichment Workflow

NEW

Introducing The Twist PCR-Free WGS Library Preparation Kit

Power your sequencing with Twist’s enzyme driven library prep; engineered to deliver more data from your sample.