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Sample GSM1888984 Query DataSets for GSM1888984
Status Public on Dec 15, 2015
Title EV RNA-seq 2
Sample type SRA
 
Source name BY4742 PUF2 null mutants
Organism Saccharomyces cerevisiae
Characteristics strain: BY4742
vector: Empty
Growth protocol Cells were grown to early log phase (0.1 -0.4 OD660) in minimal media.
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)
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2000
 
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
 
Submission date Sep 20, 2015
Last update date May 15, 2019
Contact name Douglas Porter
Organization name Stanford
Department Dermatology
Lab Khavari
Street address 269 Campus Drive
City Stanford
State/province CA
ZIP/Postal code 94305
Country USA
 
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
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 SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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