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GenomicsSt. Jude Children’s Research Hospital – Washington University Pediatric Cancer Genome Project Steering Committee
Data Access Committee EGAC00001000044
EGAC00001000044 | EGA
UnknownOpening doors to physical sample tracking and attribution in Earth and environmental sciences.
Not available
S-EPMC12181277 | biostudies-literature
GenomicsPCGP MEL RNASEQ - samples
DATA FILES FOR PCGP SJMEL RNASEQ
EGAD00001001247 | EGA
GenomicsPCGP MEL WXS - samples
DATA FILES FOR PCGP SJMEL WXS
EGAD00001001246 | EGA
GenomicsPCGP MEL-WGS - samples
DATA FILES FOR SJMEL-WGS
EGAD00001001032 | EGA
GenomicsThe Genomic Landscape of Childhood and Adolescent Melanoma
Despite remarkable advances in the genomic characterization of adult melanoma, the molecular pathogenesis of pediatric melanoma remains largely unknown. We analyzed 15 conventional melanomas (CM), 3 melanomas arising in congenital nevi (CNM), and 5 spitzoid melanomas (SM), using various platforms, i...
EGAS00001000901 | EGA
GenomicsThe Genomic Analysis of Medulloblastoma

Medulloblastoma is a heterogenous disease made up of at least four distinct subtypes of disease which appear to exploit and disrupt naturally occurring developmental pathways of cellular growth and hindbrain development. To better understand the driver mutations of this disease, we performed whol...

phs000409.v1.p1 | EGA
TranscriptomicsHigh-Resolution Genomic Profiling of Adult and Pediatric Core-Binding-Factor Acute Myeloid Leukemia Reveals New Recurrent Genomic Alterations
To identify cooperating lesions in core-binding-factor acute myeloid leukemia (CBF-AML), we performed single-nucleotide polymorphism (SNP)-array analysis on 300 diagnostic and 41 relapse adult and pediatric leukemia samples. We identified a mean of 1.28 copy number alterations (CNAs) per case at dia...
ORGANISM(S): Homo sapiens 
2012-02-07 | E-GEOD-32462 | biostudies-arrayexpress
TranscriptomicsNovel mutations target distinct subgroups of medulloblastoma.
Medulloblastoma is a malignant childhood brain tumour comprising four discrete subgroups. To identify mutations that drive medulloblastoma we sequenced the entire genomes of 37 tumours and matched normal blood. One hundred and thirty-six genes harbouring somatic mutations in this discovery set wer...
ORGANISM(S): Homo sapiens 
2012-07-05 | E-GEOD-37418 | biostudies-arrayexpress
GenomicsWhole Genome Sequencing of Pediatric Acute Megakaryoblastic Leukemia

We have performed whole genome sequencing of 4 cases of pediatric acute megakaryoblastic leukemia to identify somatic genetic alterations driving leukemogenesis.

phs000413.v1.p1 | EGA
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