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RNAseq of GBM tumors with SAT1 knockout
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2025-03-20
相关数据集
ena-DATASET-UCSF-04-08-2016-08:17:32:265-117 - samples
We performed bulk exome-seq on a primary GBM and a blood sample from SF10345EGA dataset EGAD00001002273
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Additional file 8 of Whole-genome sequencing of glioblastoma reveals enrichment of non-coding constraint mutations in known and novel genes
Additional file 8: Table S7. Annotation of the NCCMs associated with the DYNC1I1 gene based on data from the ENCODE portal and the UCSC Browser databases.
Figshare2020-07-31 更新40
Prevalence of Copy-number neutral LOH in glioblastomas revealed by analysis of laser-microdissected tissues
Prevalence of Copy-number neutral LOH in glioblastomas revealed by analysis of laser-microdissected tissues
ChEBI2009-03-01 更新30
Additional file 1: Table S1. of Evidence for L1-associated DNA rearrangements and negligible L1 retrotransposition in glioblastoma multiforme
RC-seq output summary. Table S2. Polymorphic and somatic L1 mutations called by TEBreak. Table S3. List of somatic L1 mutations and PCR validation information. Table S4. GBM cell line transfection eff
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Integrative Genome-wide Analysis of Glioblastoma.
Glioblastoma multiforme shows multiple chromosomal aberrations, the impact of which on gene expression remains unclear. To investigate this relationship and to identify putative initiating genomic eve
NIAID Data Ecosystem40
