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Status |
Public on Jun 18, 2012 |
Title |
Oocyte litter 1 |
Sample type |
SRA |
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Source name |
oocyte
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Organism |
Mus musculus |
Characteristics |
genetic background: mixed strain oocytes cell type: oocyte crosses: LSD1 FL/FL mice (From Wang et al, Nature 446, 2007 ) were crossed with ZP3::Cre mice (Jax labs strain 003651) and backcrossed again to generate LSD1 FL/FL, ZP3Cre+ and - mice. FOr this study, only LSD1 FL/FL, ZP3::Cre negative females were used to produce oocytes. For 2C embryos, these females were crossed with wild type CB6 males
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Treatment protocol |
Oocytes were collected by E0.5 and lysed in Prelude Direct Lysis Buffer
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Growth protocol |
Females were superovulated using standard conditions
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Extracted molecule |
total RNA |
Extraction protocol |
Nugen Ovation RNA-Seq kit(for amplifying RNA) followed by library construction using Illumina mRNA sample prep kit starting with end repair
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina Genome Analyzer II |
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Description |
RNA amplified using SPIA
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Data processing |
Oocyte_1.wig; genome build: mm9 Bowtie alignments, allowing 3 mismatches per read, allowing up to 20 alignments per read
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Submission date |
Nov 23, 2011 |
Last update date |
May 15, 2019 |
Contact name |
Todd Macfarlan |
E-mail(s) |
macfarlan@salk.edu
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Organization name |
The Salk Institute
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Street address |
10010 North Torrey Pines
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City |
La Jolla |
State/province |
CA |
ZIP/Postal code |
92037 |
Country |
USA |
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Platform ID |
GPL9250 |
Series (2) |
GSE33922 |
RNA-Seq from wt oocytes |
GSE33923 |
2C::tomato ES cells, 2-cell embryos and wild type oocytes |
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Relations |
SRA |
SRX109434 |
BioSample |
SAMN00760873 |
Supplementary file |
Size |
Download |
File type/resource |
GSM838743_Oocyte_1.bed.gz |
52.6 Mb |
(ftp)(http) |
BED |
SRA Run Selector |
Raw data are available in SRA |
Processed data provided as supplementary file |
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