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品牌 | illumina/美国因美纳 | 货号 | TG-141-1005 |
---|---|---|---|
规格 | 1 kit | 供货周期 | 两周 |
主要用途 | 小型全基因组测序 组合试剂 试剂盒 | 应用领域 | 医疗卫生,化工,生物产业,制药 |
"Illumina/TG TruSight Inherited Disease Sequencing Panel (48 Samples)/TG-141-1005/1 Ea
" TG-141-1005 Illumina 产品编号: TG-141-1005美 元 价: $0.00会 员 价: 待定品 牌: Illumina产 地: 美国公 司: Illumina, Inc.产品分类: 其它>其它试剂>芯片公司分类: Clinical Research Products "Product Highlights:
Developed in collaboration with Dr. Stephen Kingsmore and team during his tenure at Children's Mercy Hospital (CMH) for Pediatric Genomic Medicine, Dr. Carol Saunders at CMH, and Dr. Hilger Ropers at the Max Planck Institute
Targets 552 genes, including coding exons, intron-exon boundaries, and regions known to harbor pathogenic mutations
TruSight Inherited Disease was initially based on a 448 disease panel designed for preconception carrier testing for severe, recessive childhood diseases published by Dr. Kingsmore and team in Science Translational Medicine1.
The original content was revised by Dr. Saunders, FACMG, at CMH (following ACMG guidelines for testing ultra-rare genetic diseases) to reflect the needs of medical geneticists with a primary focus on severe recessive diseases with childhood onset. Intellectual disABIlity genes were added by Dr. Ropers.
The TruSight Inherited Disease sequencing panel set includes custom oligos targeting identified regions of interest. Sufficient product is supplied for four enrichment reactions.
Specifications:
Input Quantity 50 ng DNA
System Compatibility MiSeq,NextSeq 550,MiSeqDx in Research Mode,MiniSeq,NextSeq 500,HiSeq 2500
Variant Class Single Nucleotide Polymorphisms (SNPs),Germline Variants
Specialized Sample Types Low Input
Technology Sequencing
Species Category Human
Method Targeted DNA Sequencing"
Illumina公司,致力于新一代测序和芯片技术的生产与开发,提供产品与应用资讯
Illumina公司创立于1998年4月,是遗传变异和生物学功能分析领域的优秀的产品、技术和服务供应商。通过帮助客户加快实现生物信息的采集、分析和应用,来改善人类健康。
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