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Status |
Public on Dec 15, 2015 |
Title |
EV RNA-seq 2 |
Sample type |
SRA |
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Source name |
BY4742 PUF2 null mutants
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Organism |
Saccharomyces cerevisiae |
Characteristics |
strain: BY4742 vector: Empty
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Growth protocol |
Cells were grown to early log phase (0.1 -0.4 OD660) in minimal media.
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Extracted molecule |
polyA RNA |
Extraction protocol |
RNA was extracted from 50 ml culture by the hot phenol method, followed by an RNA-cleanup column. TruSeq Stranded mRNA Sample Preparation Guide Rev E was followed to prepare libraries for sequencing: Poly-A selection, Fragment, Prime, Finish using FPF mix (Frag 6 minutes), cDNA Synthesis, and finally bead purification (Agencourt AMPure XP)
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 2000 |
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Data processing |
Reads were mapped to the EF4 genome using bowtie2 –local Reads assigned to genes using HTSeq and the EF4 genomic annotation Differential gene expression was determined using DESeq2 Genome_build: EF4 Supplementary_files_format_and_content: Processed data files represent the absolute number of reads (not normalized) in each gene, as determined by HTSeq
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Submission date |
Sep 20, 2015 |
Last update date |
May 15, 2019 |
Contact name |
Douglas Porter |
Organization name |
Stanford
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Department |
Dermatology
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Lab |
Khavari
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Street address |
269 Campus Drive
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City |
Stanford |
State/province |
CA |
ZIP/Postal code |
94305 |
Country |
USA |
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Platform ID |
GPL13821 |
Series (2) |
GSE73227 |
The binding specificity and regulatory effect of WT and redesigned Puf2p [RNA-Seq] |
GSE73274 |
The binding specificity and regulatory effect of WT and redesigned Puf2p |
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Relations |
BioSample |
SAMN04099019 |
SRA |
SRX1267199 |
Supplementary file |
Size |
Download |
File type/resource |
GSM1888984_EV-2.txt.gz |
33.8 Kb |
(ftp)(http) |
TXT |
SRA Run Selector |
Raw data are available in SRA |
Processed data provided as supplementary file |
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