|
Status |
Public on Apr 10, 2019 |
Title |
Vecad_3 |
Sample type |
SRA |
|
|
Source name |
VEcad-cre;LoxP-tdTomato
|
Organism |
Mus musculus |
Characteristics |
source: bone marrow cell type: non-hematopoietic VEcad+ age: 4-12 weeks
|
Extracted molecule |
polyA RNA |
Extraction protocol |
RNeasy Micro Kit - QIAGEN SMART-Seq v4 Ultra Low Input RNA Kit - Clontech
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 2500 |
|
|
Description |
counts.niche.raw.csv.gz counts.niche.normalized.csv.gz
|
Data processing |
Base calling and demultiplexing was performed using Illumina bcl2fastq software. The sequencing reads were aligned to the mouse genome (build mm10/GRCm38) using the splice-aware STAR aligner. The featureCounts program was utilized to generate counts for each gene. The raw counts were normalized using the DESeq2 R package. Genome_build: mm10 Supplementary_files_format_and_content: CSV files contain raw and normalized counts for all genes and samples.
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|
|
Submission date |
Jan 08, 2018 |
Last update date |
Apr 10, 2019 |
Contact name |
Igor Dolgalev |
Organization name |
NYU Grossman School of Medicine
|
Street address |
550 1st Ave
|
City |
New York |
State/province |
New York |
ZIP/Postal code |
10016 |
Country |
USA |
|
|
Platform ID |
GPL17021 |
Series (2) |
|
Relations |
BioSample |
SAMN08327932 |
SRA |
SRX3541331 |