|
Status |
Public on Aug 08, 2019 |
Title |
RNAseq wt_2 [1223] |
Sample type |
SRA |
|
|
Source name |
wiltype iPSC-derived neurons
|
Organism |
Homo sapiens |
Characteristics |
cell line background: 7889SA parental cell line cell line source: 80 day old cortical neurons cell type: co-isogenic iPS cells mutation: none
|
Growth protocol |
induction and maturation of cortical neurons from iPS cells (total of 80 days in vitro; detailed protocol in accompanying paper)
|
Extracted molecule |
total RNA |
Extraction protocol |
Trizol extraction, rRNA removal via Ribo-Zero treatment, DNAse-digestion Illumina High-Throughput TruSeq
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 2500 |
|
|
Data processing |
alignment with STAR (default mode) Genome_build: hg19 Supplementary_files_format_and_content: combined ReadsPerGene STAR output files (containing uniquely aligned reads per gene)
|
|
|
Submission date |
Mar 15, 2019 |
Last update date |
Aug 08, 2019 |
Contact name |
Claudia Scheckel |
E-mail(s) |
[email protected]
|
Organization name |
University Hospital Zurich
|
Department |
Institute of Neuropathology
|
Street address |
Schmelzbergstrasse 12
|
City |
Zurich |
State/province |
NY |
ZIP/Postal code |
8091 |
Country |
Switzerland |
|
|
Platform ID |
GPL16791 |
Series (2) |
GSE128343 |
A large panel of isogenic APP and PSEN1 mutant human iPSC neurons reveals shared endosomal abnormalities mediated by APP b-CTFs, not Ab [RNA-seq] |
GSE128345 |
A large panel of isogenic APP and PSEN1 mutant human iPSC neurons reveals shared endosomal abnormalities mediated by APP b-CTFs, not Ab |
|
Relations |
BioSample |
SAMN11130418 |
SRA |
SRX5524958 |