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"Illumina/TruSight Myeloid Sequencing Panel (96 samples)/FC-130-1010/1 Ea

" FC-130-1010 Illumina 產(chǎn)品編號(hào)： FC-130-1010美  元  價(jià)： $0.00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(lèi)： 其它>其它試劑>芯片公司分類(lèi)： Clinical Research Products "Product Highlights:

The TruSight Myeloid Sequencing Panel uses expert-defined content and proven next-generation sequencing (NGS) technology to identify somatic variants in myeloid malignancies.

The panel content was designed by a consortium of recognized experts in blood cancer disorders and targets genes frequently mutated in:

Acute myeloid leukemia (AML)

Myelodysplastic syndrome (MDS)

Myeloproliferative neoplasms (MPN)

Chronic myelogenous leukemia (CML)

Chronic myelomonocytic leukemia (CMML)

Juvenile myelomonocytic leukemia (JMML)

The TruSight Myeloid Sequencing Panel covers 15 full genes (exons only) and 39 additional genes where oncogenic hotspots are covered, providing a comprehensive assessment of the key genes known to be involved in myeloid malignancies in a single test. The result is an accurate, cost-effective solution that enables researchers to profile liquid tumors.

View the gene list

TruSight Myeloid libraries are ideally suited to run on a desktop sequencer and perform alignment and variant calling with the MiSeq Reporter or Local Run Manager Amplicon workflow with Somatic Variant Caller. Filtering and annotation can then be performed using the following Illumina annotation and filtering tools: BaseSpace Variant Interpreter or VariantStudio.

Specifications:

Assay Time 8 hours

Hands-On Time 3 hours

Input Quantity 50 ng

System Compatibility MiSeq,MiSeqDx in Research Mode,MiniSeq,NextSeq 500

Technology Sequencing

Variant Class Somatic Variants,Insertions-Deletions (indels)

Species Category Human

Cancer Type Hematological

Method Amplicon Sequencing,Targeted DNA Sequencing"

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Illumina 測(cè)序組合試劑盒 中國(guó)銷(xiāo)售