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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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