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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.

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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
EGAF50000808628 fq.gz 3.8 GB
EGAF50000808629 fq.gz 3.7 GB
EGAF50000808630 fq.gz 4.8 GB
EGAF50000808631 fq.gz 4.8 GB
EGAF50000808632 fq.gz 7.5 GB
EGAF50000808633 fq.gz 5.5 GB
EGAF50000808634 fq.gz 5.5 GB
EGAF50000808635 fq.gz 7.8 GB
EGAF50000808638 fq.gz 7.6 GB
EGAF50000808639 fq.gz 8.0 GB
10 Files (59.1 GB)