簡(jiǎn)要描述:Illumina/Infinium Staining Rack (1)/WG-10-207/1 Ea上海易匯生物科技有限公司于17年正式銷售Illumina公司基因芯片、二代測(cè)序NGS測(cè)序儀及相關(guān)測(cè)序試劑盒等產(chǎn)品Sequencing Kits/ Microarray Kits/Informatics ProductsIllumina 測(cè)序組合試劑盒 EGMK81312
詳細(xì)介紹
品牌 | illumina/美國(guó)因美納 | 規(guī)格 | 1 kit |
---|---|---|---|
供貨周期 | 兩周 | 主要用途 | 小型全基因組測(cè)序 組合試劑 試劑盒 |
應(yīng)用領(lǐng)域 | 醫(yī)療衛(wèi)生,化工,生物產(chǎn)業(yè),制藥 |
Illumina 測(cè)序組合試劑盒 EGMK81312
Illumina公司,致力于新一代測(cè)序和芯片技術(shù)的生產(chǎn)與開(kāi)發(fā),提供產(chǎn)品與應(yīng)用資訊
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Sequencing Kits/ Microarray Kits/Informatics Products/ Clinical Research Products/In Vitro Diagnostic/ Products/Molecular Biology Reagents/ Accessory Products
上海易匯生物科技有限公司于17年正式銷售Illumina公司基因芯片、二代測(cè)序NGS測(cè)序儀及相關(guān)測(cè)序試劑盒等產(chǎn)品
咨詢illumina MiSeq測(cè)序試劑盒等產(chǎn)品歡迎您致電 上海易匯生物科技有限公司:1850 1609 238張經(jīng)理
Illumina 測(cè)序組合試劑盒 EGMK81312
產(chǎn)品編號(hào): EGMK81312美 元 價(jià): $1009.00會(huì) 員 價(jià): 待定品 牌: Illumina產(chǎn) 地: 美國(guó)公 司: Illumina, Inc.產(chǎn)品分類: 分子類>二代測(cè)序>DNA文庫(kù)制備試劑盒公司分類: Library Preparation Kits
"Product Highlights:
Unlock small samples (50–100 ng DNA input)
CpG, CHH, & CHG regions included for comprehensive, whole-genome results
Fast protocol – five-hour method
Capture full sample diversity
Sequence the entire sample–no loss of information
The process of bisulfite treatment denatures genomic DNA into single stranded DNA. TruSeq DNA Methylation converts single stranded DNA into an Illumina sequencing library. All ssDNA fragments are captured into an Illumina sequencing library, therefore eliminating the loss of diversity associated with other methods.
Supported analysis in the cloud
TruSeq DNA Methylation libraries can be aligned to the human genome and compared for differential methylation with Illumina BaseSpace Apps MethylSeq and MethylKit. These applications are fully supported and were developed specifically for TruSeq DNA Methylation library preparation.
Example data sets for TruSeq DNA Methylation libraries, also available in BaseSpace Sequence Hub Data Central (use the “Methyl Seq” category filter), demonstrate unparalleled quality and seamless analysis.
Deep coverage of critical genomic regions
Depth of coverage is enhanced in genomic areas with BIOLOGical utility. TruSeq DNA Methylation captures full sample diversity of critical areas, including:
Coding region start and end for exons from the canonical transcript of protein coding genes for genes known to be involved in cancer, taken from SOMA and CRUK panels (as well as literature-derived cancer genes)
Genes defined by the American College of Medical Genetics as being medically relevant (ACMG genes)
Exonic coding regions from Ensemble 70
List of 100 promoters defined by the Broad Institute as being of high interest and difficult to sequence"
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