ClearSeq Noonan Syndrome
ClearSeq 罕見疾病 Noonan syndrome 相關基因分析
ClearSeq Noonan Syndrome is a next generation sequencing panel designed using information from published literature and the NIH resource GeneReviews. This panel is designed to detect genetic mutations known to be associated with Noonan syndrome and related disorders such as LEOPARD, cardio-facio-cutaneous syndrome, and Costello syndromes.Compatible with HaloPlexHS and HaloPlex Target Enrichment Systems
ClearSeq Noonan Syndrome
Target a comprehensive set of kinases and kinase related transcripts for enrichment, including over 500 kinases and 612 genesCompatible with HaloPlex
產品列表
| 貨號 | 產品 | 數量 | |
|---|---|---|---|
| G9954C | ClearSeq Made-to-Order Panels, HS | 48 rxns | |
| G9954B | ClearSeq Made-to-Order Panels, HS | 96 rxns | |
| G9953C | ClearSeq Made-to-Order Panels | 48 rxns | |
| G9953B | ClearSeq Made-to-Order Panels | 96 rxns |
ClearSeq Noonan Syndrome
- Expert-optimized content - Highly targeted content enabling analysis of regions implicated in rare disease pathogenesis
- Fast track to answers - Proven, high-performing capture oligos are coupled with highly efficient SureSelect and HaloPlex workflows, providing faster time to results and compatibility with samples of limited availability (high throughput or benchtop sequencers)
- Comprehensive Workflow Solution - Accelerated sample to categorized variants with SureCall
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