Whole Exome Sequencing of Multiple Myeloma Patients

We used whole exome sequencing (WES) data from 35 MM patients to evaluate possible mutational signatures and driver mutations associated with the patient’s clinical and cytogenetic characteristics.

Type: Exome Sequencing
Archiver: European Genome-Phenome Archive (EGA)

1 Dataset

Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data

Dataset ID	Description	Technology	Samples
EGAD50000000578	Here, we provide mapped cram files from 35 multiple myeloma patients. Sequencing was performed employing Illumina's short read technology. Resulting sequencing data was mapped against GRCh38 using nfcore/sarek v3.2.3.	Illumina NovaSeq 6000	35