Targeted capture, whole genome sequencing, and RNAseq to identify rearrangements in B-cell lymphomas
This study contains whole genome and custom targeted capture sequencing of mature B-cell lymphomas (DLBCL, FL, BL, HGBCL-DH-BCL2, HGBCL-DH-BCL6) to identify translocation breakpoints of common oncogene rearrangements (MYC, BCL2, BCL6). It is complemented by RNAseq data where available. Complete details are available in the publication Hilton et al, 2024, Blood. Capture sequencing: 357 samples; 364 unique libraries; cram file format aligned to hg38 Whole genome sequencing: 12 samples; 12 unique libraries; cram file format aligned to grch37 RNAseq: 257 samples; 257 unique libraries; fastq file format
- Type: Cancer Genomics
- Archiver: European Genome-Phenome Archive (EGA)
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 |
---|---|---|---|
EGAD50000000474 | Illumina NovaSeq X | 12 | |
EGAD50000000489 | Illumina HiSeq X | 364 | |
EGAD50000000496 | Illumina NovaSeq X | 257 |
Publications | Citations |
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High-resolution architecture and partner genes of <i>MYC</i> rearrangements in lymphoma with DLBCL morphology.
Blood Adv 2: 2018 2755-2765 |
47 |
Motive and Opportunity: MYC rearrangements in high-grade B-cell lymphoma with MYC and BCL2 rearrangements-an LLMPP study.
Blood 144: 2024 525-540 |
2 |