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Myelodysplastic Syndromes

Myelodysplastic syndromes (MDS) are precursors to leukemias, with one third of patients developing acute myeloid leukemia in five years or less. With little known about the cause of the disease, novel technologies leveraging single-cell genomics reveal missing details that are lost in bulk sequencing. Uncover clonal evolution insights with precision download the MDS Tapestri panel today.

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Panel Details

Tapestri Single-cell DNA Myelodysplastic Syndromes (MDS) Panel

Advance your understanding of the genetic heterogeneity underpinning myelodysplastic syndromes (MDS) by targeting 21 genes with 148 amplicons for single-cell sequencing. Covering a combination of oncogenes and tumor suppressor genes, this panel is designed to cover some of the most commonly mutated genes associated with MDS

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Want to modify this panel?

Use Tapestri Designer to add or remove content from existing catalog panels and make this panel your own with content that is relevant to your research. Or start from scratch and upload your human (hg19) or mouse (mm10) targets using gene names, genomic coordinates, or SNV IDs. Target anywhere in the whole human or mouse genome and advance your research with targeted single-cell DNA sequencing.

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