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Acute Lymphoblastic Leukemia

ALL is the most common type of cancer in children, which like other cancers is caused by complex genetic mutations. As this complex disease evolves, understanding genetic variability — including mutation co-occurrence at the single-cell level — is vitally important in order for clinical researchers to break the cycle of treatment response, resistance, and relapse.


Panel Details

Tapestri Single-cell DNA Acute Lymphoblastic Leukemia (ALL) Panel

Advance your understanding of the genetic heterogeneity underpinning acute lymphoblastic leukemia (ALL) by targeting 107 genes with 283 amplicons for single-cell sequencing. Incorporating a combination of oncogenes and tumor suppressor genes, this panel is designed to cover some of the most commonly mutated genes associated with ALL.

To view and download panel content and coordinates using Tapestri Designer, click here.

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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