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Status |
Public on Jan 25, 2021 |
Title |
testis transcriptome experimental mouse 2 |
Sample type |
SRA |
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Source name |
testis
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Organism |
Mus musculus |
Characteristics |
strain: C57BL/6J mutation: Homozygous Ret (V805A) treatment: injected for 9 days with vehicle [saline:cremophor:ethanol (7:2:0.9)] containing 1NaPP1-HCl at 4/465 mg/ml, 10 microliters per gram body weight age: ~120 days
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Treatment protocol |
Control mice were injected with 10 microliters per gram body weight with saline:cremophor:ethanol (7:2:0.9). Experimental mice were injected with vehicle in which was dissolved 1NaPP1-HCl at 4/465 mg/ml vehicle. Injections continued daily for 9 days total. Mice were allowed to recover for 5 days prior to testis dissection (experiment day 14).
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Growth protocol |
standard mouse facility
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Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted with the Qiagen RNAeasy Mini kit. Diretional RNA-seq libraries were prepared from 500ng total RNA using the NEBNext Directional Ultra RNA Library Prep Kit for Illumina (New England Biolabs), with initial polyA+ isolation.
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NextSeq 500 |
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Description |
gene_exp.diff: E_1 genes.read_group_tracking: E_1
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Data processing |
Illumina pipeline software v1.8 was used for base calling. cutadapt v1.8 (-m 20 -q 20 -a AGATCGGAAGAGCACACGTCTGAACTCCAGTC --match-read-wildcards) was used to trim and filter reads. tophat v2.0.13 (--no-novel-juncs --library-type fr-firststrand) was used to map reads to the mouse mm10 reference genome+transcriptome (UCSC). cuffquant (--library-type fr-firststrand) was used to quantify transcripts based on the mouse mm10 reference genome+transcriptome (UCSC). cuffdiff v2.2.1 was used to call differentially expressed genes based on the mouse mm10 reference genome+transcriptome (UCSC). Genome_build: Mouse mm10 (UCSC) Supplementary_files_format_and_content: Tab delimited text files are standard cuffdiff2 output files for gene-level analysis, including counts, FPKM values, and q-values for differential expression testing (corrected for multiple hypothesis testing). The 'gene_exp.diff' file contains average FPKM values for each pair of replicates as well as results for statistical testing for differential expression. The 'genes.read_group_tracking' file contains raw mapped read counts and FPKM values for individual samples.
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Submission date |
Mar 06, 2018 |
Last update date |
Jan 25, 2021 |
Contact name |
Jennifer K Grenier |
Organization name |
Cornell University
|
Department |
Biomedical Sciences
|
Lab |
Biotechnology Building rm 333
|
Street address |
526 Campus Rd
|
City |
Ithaca |
State/province |
NY |
ZIP/Postal code |
14853 |
Country |
USA |
|
|
Platform ID |
GPL19057 |
Series (1) |
GSE111487 |
Effect of 9 days of inhibited GDNF signaling on the transcriptome of the mouse testis |
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Relations |
BioSample |
SAMN08640202 |
SRA |
SRX3768780 |