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Data · dataset · 2022

Linked-read whole-genome sequencing resolves common and private structural variants in multiple myeloma

Listed in Researchdata.se

This repository contains 10x Chromium linked-read WGS (lrWGS), RNAseq and H3K27Ac ChIPseq from multiple myeloma.

Description

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)

Links

Where it is published

Catalogue records · 1

Topics

Inferred from text
Cancer 65% · Genome sequencing 65% · RNA sequencing 65% · Sequencing 75%
Provenance · 1 source records, 11 field assertions
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Researchdata.seoai:researchdata.se:doi-10-17044-scilifelab-17049059/011 d agoJSON v1
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concepts[modality].local:modality:genome-sequencingenrichment · researchdata sekeyword-concept-rules@1.0.0title+description (65%)
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