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Status |
Public on May 26, 2015 |
Title |
Hnrnpu mutant rep2 |
Sample type |
SRA |
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Source name |
Heart, Hnrnpu mutant
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Organism |
Mus musculus |
Characteristics |
strain/background: C57BL/6 & 129 S4 mix genotype/variation: hnrnpu mutant tissue: ventricle age: postnatal day 14 gender: female
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Treatment protocol |
N/A
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Growth protocol |
N/A
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Extracted molecule |
total RNA |
Extraction protocol |
Whole hearts were dissected from P14 mice of distinct genotypes, atria were removed. Total RNAs were extracted from ventricles by Trizol extraction protocol. 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 HiSeq 2500 |
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Description |
MT_2
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Data processing |
Illumina Casava1.7 software used for basecalling. Sequenced reads were trimmed for adaptor sequence, masked for low-complexity or low-quality sequence, and then mapped to the mm9 whole genome using Bowtie v0.12.9 with parameters -X 20000 -k 2 -m 2 -q -p Reads Per Kilobase of exon per Megabase of library size (RPKM) were calculated using a protocol from Mortazavi et al., Nat Methods, 2008. Differential gene expression was calculated using the R statistical package DESeq. Genome_build: MGSCv37 (mm9) Supplementary_files_format_and_content: hnrnpu-heart-P14.xlsx: Tab-delimited text file includes RPKM values for each Sample.
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Submission date |
Apr 22, 2015 |
Last update date |
May 15, 2019 |
Contact name |
Sean O'Keeffe |
E-mail(s) |
so2346@columbia.edu
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Organization name |
Columbia University
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Street address |
701 West 168th Street
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City |
New York |
ZIP/Postal code |
10032 |
Country |
USA |
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Platform ID |
GPL17021 |
Series (1) |
GSE68178 |
hnRNP U protein is required for normal pre-mRNA splicing and postnatal heart development and function |
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Relations |
BioSample |
SAMN03497962 |
SRA |
SRX1004795 |
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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