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GenomicsCopy number profiling of primary samples and cell lines of retinoblastoma
While RB1 loss initiates retinoblastoma development, additional somatic copy number alterations (SCNAs) can drive tumor progression. Although SCNAs have been identified with good concordance between studies at a cytoband resolution, accurate identification of single genes for all recurrent SCNAs is ...
EGAS00001001715 | EGA
GenomicsWhole exome sequencing on primary retinoblastoma tissues and matching lymphocyte DNA.
Retinoblastoma is a rare childhood cancer initiated by RB1 mutation or MYCN amplification, while additional alterations may be required for tumor development. However, the view on single nucleotide variants is very limited. To better understand oncogenesis, we determined the genomic landscape of ret...
EGAS00001001690 | EGA
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