Linked-read whole-genome sequencing resolves common and private structural variants in multiple myeloma
收藏DataCite Commons2025-01-15 更新2025-04-16 收录
下载链接：
https://figshare.scilifelab.se/articles/dataset/Linked-read_whole-genome_sequencing_resolves_common_and_private_structural_variants_in_multiple_myeloma/17049059/1
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资源简介：
This repository contains 10x Chromium linked-read WGS (lrWGS), RNAseq and H3K27Ac ChIPseq from multiple myeloma.
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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.
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The data set contains sensitive human genomic data and is under restricted access. Request for access can be made to datacentre@scilifelab.se.
提供机构：
Karolinska Institutet
创建时间：
2022-06-14
