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Status |
Public on Jan 26, 2024 |
Title |
EPEN_SPEPN_000UT_00002846_DR |
Sample type |
SRA |
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|
Source name |
Spinal ependymoma (FFPE tissue)
|
Organism |
Homo sapiens |
Characteristics |
tissue: Spinal ependymoma (FFPE tissue)
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA of SP-EPN was isolated from FFPE tissues using the Maxwell® RSC RNA FFPE Kit (Promega). Concentrations were measured with a Qubit 2.0 Fluorometer (Thermo Fisher Scientific) and RNA integrity was analyzed using the RNA 6000 Nano Kit on a 2100 Bioanalyzer (Agilent Technologies). Library preparation was conducted using the SMART-Seq Stranded Kit (Takara Bio)
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NovaSeq 6000 |
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Data processing |
Pre-processing was started by checking RNA sequencing read quality using FASTQC (v0.11.9) and subsequently aligned to the human reference genome assembly (GRCh38.106) using STAR aligner (v2.7.10a) in default 1-pass mode. Mapped reads were quantified using featureCounts (v1.6.0) as part of the Subread software package. The “isPairedEnd” parameter was specified in default “unstranded” read counting mode. Assembly: GRCh38.106 Supplementary files format and content: The count matrix is provided as non-normalized and unfiltered raw read counts.
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Submission date |
Sep 12, 2023 |
Last update date |
Jan 26, 2024 |
Contact name |
Karoline Hack |
E-mail(s) |
hack@kinderkrebs-forschung.de
|
Organization name |
University Medical Center Hamburg-Eppendorf
|
Department |
Children's Cancer Center Hamburg
|
Lab |
Schüller
|
Street address |
Martinistraße 52
|
City |
Hamburg |
ZIP/Postal code |
20251 |
Country |
Germany |
|
|
Platform ID |
GPL24676 |
Series (2) |
GSE242992 |
Transcriptomic and epigenetic dissection of spinal ependymomas (SP-EPN) identifies clinically relevant subtypes enriched for tumors with and without NF2 mutation [RNA-seq] |
GSE242994 |
Transcriptomic and epigenetic dissection of spinal ependymoma (SP-EPN) identifies clinically relevant subtypes enriched for tumors with and without NF2 mutations |
|
Relations |
BioSample |
SAMN37366018 |
SRA |
SRX21761896 |