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Article

Whole Genome Sequencing-Based Discovery of Structural Variants in Glioblastoma.

Methods in molecular biology (Clifton, N.J.) - 1 Jan 2018

Wrzeszczynski Kazimierz O, Felice Vanessa, Shah Minita, Rahman Sadia, Emde Anne-Katrin, Jobanputra Vaidehi, O Frank Mayu, Darnell Robert B

Abstract excerpt

Next-generation DNA sequencing (NGS) technologies are currently being applied in both research and clinical settings for the understanding and management of disease. The goal is to use high-throughput sequencing to identify specific variants that drive tumorigenesis within each individual's tumor genomic profile. The significance of copy number and structural variants in glioblastoma makes it essential to broaden...

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Source

Identifiers

PMID: 29392687
DOI: 10.1007/978-1-4939-7659-1_1

Genes

EGFR

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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