Study

An integrated molecular study of 20 hepatoblastoma pairs using whole genome sequencing and RNA sequencing

Study ID Alternative Stable ID Type
EGAS00001002772 Other

Study Description

Hepatoblastoma is an uncommon malignant liver cancer occurring in infants and children. The mutant background of hepatoblastoma has not been fully demonstrated. The aim of this study is to genomically depict the mutational landscape of hepatoblastoma through an integrative analysis of whole genome sequencing and RNA sequencing of 20 hepatoblastomas from Chinese individuals.

Study Datasets 1 dataset.

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Dataset ID Description Technology Samples
EGAD00001003914
This dataset provides whole genome sequencing data of tumor/normal pairs from 20 patients with hepatoblastoma using the illumina Novaseq sequencing system. It includes 40 samples (20 normals and 20 hepatoblastoma tumors). Our comprehensive analysis identified somatic mutations, structural variations, copy number variations and non-coding variants in hepatoblastoma.
Illumina NovaSeq 6000 40

Who archives the data?

There are no publications available