詳細介紹
品牌 | illumina/美國因美納 | 貨號 | TG-141-1005 |
---|---|---|---|
規格 | 1 kit | 供貨周期 | 兩周 |
主要用途 | 小型全基因組測序 組合試劑 試劑盒 | 應用領域 | 醫療衛生,化工,生物產業,制藥 |
"Illumina/TG TruSight Inherited Disease Sequencing Panel (48 Samples)/TG-141-1005/1 Ea
" TG-141-1005 Illumina 產品編號: TG-141-1005美 元 價: $0.00會 員 價: 待定品 牌: Illumina產 地: 美國公 司: Illumina, Inc.產品分類: 其它>其它試劑>芯片公司分類: 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"
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