<p>Single-cell whole genome sequencing (scWGS) provides a tool to gain deeper insights into the clonal relationships of Chr1 copy number changes. Here, we study Chr1 copy number alteration (CNA) using Direct library preparation plus (DLP+), a scalable scWGS platform implemented by image-based object recognition, and open-source computational methods. We report scWGS of 2,046 cells with 400-650 single-cells per patient from 5 Multiple Myeloma patients selected from our biobank with chr1q gains identified by iFISH using a <a href="https://www.ncbi.nlm.nih.gov/gene/1163">CKS1B</a> probe (IRB S21-01218 and I19-01384)</p>

Copy Number Abnormalities of Chr1 in Multiple Myeloma at the Single Cell    Level

Multiple Myeloma study with OTHER data on dbGaP (5 participants)

Copy Number Abnormalities of Chr1 in Multiple Myeloma at the Single Cell Level

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