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

Twist 靶向富集工作流程能够为大规模复杂基因组区域提供可扩展、低偏倚和高度均匀的覆盖;相较于基于扩增子或阵列的方法,该方案可实现更广的发现范围、更高的检测灵敏度与更强的灵活性。

  靶向富集

Twist Target Enrichment

NGS Method

amplicon

Amplicon Sequencing

NGS Method

产品

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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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.

为什么选择我们

Complete your Target

Enrichment Workflow

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推出 Twist 无 PCR WGS 文库制备试剂盒

依托 Twist 酶驱动文库制备技术赋能测序研究,专为从您的样本中获取更多数据而设计。

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