RNA sequencing data of pediatric hyperdiploid acute lymphoblastic leukemia (set 5)
The dataset includes RNA sequencing FASTQ files from diagnostic tumor samples of five hyperdiploid ALL patients (ALLT-502, ALLK-130, ALLK-134, ALLK-137, ALLK-139). Novogene's internal method was used in directional library preparation including rRNA removal. The diagnostic tumor samples were sequenced using Illumina Novaseq X Plus, and the target sequencing depth was 21 Gb per sample.
- 18/05/2026
- 5 samples
- DAC: EGAC00001001551
- Technology: Illumina NovaSeq X Plus
Two PIs (Tampere/Kuopio) and a legal representative of the Tampere University Hospital
Data will be shared if the proposed project falls within the patient/caretaker consent
Studies are experimental investigations of a particular phenomenon, e.g., case-control studies on a particular trait or cancer research projects reporting matching cancer normal genomes from patients.
| Study ID | Study Title | Study Type |
|---|---|---|
| EGAS50000001802 | RNASeq |
This table displays only public information pertaining to the files in the dataset. If you wish to access this dataset, please submit a request. If you already have access to these data files, please consult the download documentation.
| ID | File Type | Size | Quality Report |
Located in
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| EGAF50000808628 | fq.gz | 3.8 GB |
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| EGAF50000808629 | fq.gz | 3.7 GB |
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| EGAF50000808630 | fq.gz | 4.8 GB |
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| EGAF50000808631 | fq.gz | 4.8 GB |
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| EGAF50000808632 | fq.gz | 7.5 GB |
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| EGAF50000808633 | fq.gz | 5.5 GB |
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| EGAF50000808634 | fq.gz | 5.5 GB |
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| EGAF50000808635 | fq.gz | 7.8 GB |
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| EGAF50000808638 | fq.gz | 7.6 GB |
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| EGAF50000808639 | fq.gz | 8.0 GB |
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| 10 Files (59.1 GB) | ||||
