Linked-read whole-genome sequencing resolves common and private structural variants in multiple myeloma doi-10-17044-scilifelab-17049059-0 https://doi.org/10.17044/SCILIFELAB.17049059 Swedish National Data Service Svensk nationell datatjänst Landing page Linked-read whole-genome sequencing resolves common and private structural variants in multiple myeloma doi-10-17044-scilifelab-17049059-0 https://doi.org/10.17044/SCILIFELAB.17049059 Månsson, Robert Swedish National Data Service Svensk nationell datatjänst Landing page This repository contains 10x Chromium linked-read WGS (lrWGS), RNAseq and H3K27Ac ChIPseq from multiple myeloma. The data consists of fastq files from lrWGS of 37 individuals with data from tumor and matched normal tissue from 32 of them. Additionally, it contains fastq files from RNAseq of 32 of the 37 patients and H3K27Ac ChIPseq data from select patients. The data set contains sensitive human genomic data and is under restricted access. Request for access can be made to datacentre@scilifelab.se. (mailto:datacentre@scilifelab.se) Access to data through an external actor. Access to data is restricted. Åtkomst till data via extern aktör. Tillgång till data är begränsad. restrictedAccess