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GEO help: Mouse over screen elements for information. |
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Status |
Public on Jul 01, 2020 |
Title |
m1_Young1_I5 |
Sample type |
SRA |
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Source name |
three-mo mouse BEC
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Organism |
Mus musculus |
Characteristics |
cell type: primary murine brain endothelial cells
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Growth protocol |
Mice 3 (young)
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Extracted molecule |
total RNA |
Extraction protocol |
Brain tissues were dissected using Miltenyi neural dissociation kit. Brain endothelial cells were isolated via FACS. RNA libraries were prepared for sequencing using standard Illumina protocols
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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 |
Illumina Casava1.7 software used for basecalling. Sequenced reads were trimmed for adaptor sequence, and masked for low-complexity or low-quality sequence, then mapped to mm8 whole genome using bowtie v0.12.2 with parameters -q -p 4 -e 100 -y -a -m 10 --best --strata Reads Per Kilobase of exon per Megabase of library size (RPKM) were calculated using a protocol from Chepelev et al., Nucleic Acids Research, 2009. In short, exons from all isoforms of a gene were merged to create one meta-transcript. The number of reads falling in the exons of this meta-transcript were counted and normalized by the size of the meta-transcript and by the size of the library. Genome_build: mm10 Supplementary_files_format_and_content: raw count table
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Submission date |
Jul 09, 2019 |
Last update date |
Jul 01, 2020 |
Contact name |
Michelle Berkeley Chen |
E-mail(s) |
[email protected]
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Organization name |
Stanford
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Street address |
318 Campus Drive
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City |
Stanford |
ZIP/Postal code |
94325 |
Country |
USA |
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Platform ID |
GPL24247 |
Series (1) |
GSE134058 |
Circulatory proteins permeate the brain via selective transport impaired with age" |
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Relations |
BioSample |
SAMN12239661 |
SRA |
SRX6423241 |
Supplementary data files not provided |
SRA Run Selector |
Raw data are available in SRA |
Processed data are available on Series record |
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