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Oncogenomics of Malignant Peripheral Nerve Sheath Tumors

UID: 11296

Author(s): Chi, Ping*, Lee, William* * MSK affiliated

Description
Description from dbGaP:

"Malignant peripheral nerve sheath tumors (MPNSTs) are a group of highly aggressive soft tissue sarcomas that may occur sporadically, in association with neurofibromatosis type I (NF1-associated), or after radiotherapy (RT-associated). We utilized comprehensive genomic approaches and identified recurrent loss-of-function somatic alterations in the Polycomb repressive complex 2 (PRC2) core components EED or SUZ12. Genetic loss of either of these two genes results in complete loss of H3K27me3 and aberrant transcriptional programming in the affected tumors."
Subject of Study
Subject(s)
Access via dbGaP


Accession #: phs000792.v1.p1

Access Restrictions
Application Required
Access Instructions
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Publicly available data such as data dictionaries, variable summaries, documents and truncated analysis are available the public download site FTP link.
Associated Publications
Equipment Used
Illumina HiSeq 2500
Dataset Format(s)
PDF, XML, TAR, gzip, TXT
Dataset Size
833.99 MB
Data Catalog Record Updated
2024-07-10