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RNA sequencing data of pediatric hyperdiploid acute lymphoblastic leukemia (set 3)

The dataset includes RNA sequencing FASTQ files from diagnostic tumor samples of five hyperdiploid ALL patients (ALLT-364, ALLT-367, ALLT-368, ALLT-371, ALLT-377). NEBNext Ultra Directional RNA Library Prep Kit (New England Biolabs) was used in library preparation, and TruSeq Stranded Total RNA Library Prep (Illumina) kit was utilized for rRNA removal. The diagnostic tumor samples were sequenced using Illumina Novaseq 6000, 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
EGAF50000808642 fq.gz 5.9 GB
EGAF50000808643 fq.gz 5.8 GB
EGAF50000808644 fq.gz 6.3 GB
EGAF50000808645 fq.gz 5.6 GB
EGAF50000808648 fq.gz 5.5 GB
EGAF50000808649 fq.gz 6.5 GB
EGAF50000808650 fq.gz 6.9 GB
EGAF50000808651 fq.gz 5.9 GB
EGAF50000808652 fq.gz 6.3 GB
EGAF50000808653 fq.gz 5.5 GB
10 Files (60.2 GB)