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Series GSE128300 Query DataSets for GSE128300
Status Public on May 13, 2019
Title Transcriptomes distinguish human FCD subtypes
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary Focal Cortical Dysplasia (FCD) is a major cause of drug-resistant focal epilepsy in children and the clinico-pathological classification remains a challenging issue in daily practice. With the recent progress in DNA methylation based classification of human brain tumors we examined, whether genomic DNA methylation and gene expression analysis can be used to also distinguish human FCD subtype
 
Overall design DNA methylomes and transcriptomes were generated from massive parallel sequencing in 15 surgical FCD specimens, matched with 5 epilepsy and 8 non-epilepsy controls.
 
Contributor(s) Kobow K, Ziemann M, Harikrishnan KN, Khurana I, Mühlebner A, Feucht M, Hainfellner JA, Czech T, Aronica E, Pieper T, Holthausen H, Kudernatsch M, Hamer H, Kasper BS, Rössler K, Conti V, Guerrini R, Coras R, Blümcke I, El-Osta A, Kaspi A
Citation(s) 31074842
Submission date Mar 14, 2019
Last update date May 13, 2019
Contact name Assam El-Osta
Organization name Baker Heart and Diabetes Institute
Lab Human Epigenetics
Street address 75 Commercial Road
City Melbourne
ZIP/Postal code 3004
Country Australia
 
Platforms (1)
GPL10999 Illumina Genome Analyzer IIx (Homo sapiens)
Samples (28)
GSM3670903 KK1-RNA
GSM3670904 KK3-RNA
GSM3670905 KK4-RNA
This SubSeries is part of SuperSeries:
GSE128301 Transcriptome and Genomic DNA methylation distinguishes human FCD subtypes
Relations
BioProject PRJNA527060
SRA SRP188422

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Supplementary file Size Download File type/resource
GSE128300_RNAstrandedRev_simp_2019.mx.txt.gz 1.5 Mb (ftp)(http) TXT
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Raw data are available in SRA
Processed data are available on Series record

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