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Sample GSM2054822 Query DataSets for GSM2054822
Status Public on Mar 12, 2016
Title RNA-Seq of rrp6 deletion (with Chd1-Ume6)- 2
Sample type SRA
 
Source name W303
Organism Saccharomyces cerevisiae
Characteristics strain background: W303
genotype/variation: rrp6 deletion with Chd1-Ume6
isolate number: isolate 2
presence of chd1-ume6 fusion: yes
Growth protocol cells were grown to OD600 0.4 to 0.6
Extracted molecule total RNA
Extraction protocol RNA was extracted with hot acid phenol, treated with Dnase I, and depleted of rRNA
Strand-specific libraries were prepared according to dUTP method and TruSeq (Illumina) Sample Prep Kit
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina Genome Analyzer
 
Data processing Basecalling was performed by Illumina CASAVA software package
Reads were mapped to S. cerevisiae genome (Saccharomyces_cerevisiae.EF4.65.dna.toplevel.fa) appended with ERCC Spike-in Control reads (https://tools.lifetechnologies.com/content/sfs/manuals/ERCC92.zip) using TopHat2
Mapped reads were filtered using SAMtools flags -f 3 -F 256
Differential transcript analysis was performed using CuffDiff (cufflinks 2.2.1) with a maskfile for rRNA and tRNA
Independent isolates were merged
Genome_build: Saccharomyces_cerevisia.EF4.65
 
Submission date Feb 04, 2016
Last update date May 15, 2019
Contact name Jeffrey N McKnight
E-mail(s) jmcknig2@uoregon.edu
Organization name University of Oregon
Department Institute of Molecular Biology
Lab McKnight Lab
Street address 1229 University of Oregon, 1318 Franklin Blvd, Rm 273 Onyx Bridge
City Eugene
State/province OR
ZIP/Postal code 97408
Country USA
 
Platform ID GPL9134
Series (2)
GSE72571 Sequence-Targeted Nucleosome Sliding in vivo - Transcription Profiling
GSE72572 Sequence-Targeted Nucleosome Sliding in vivo
Relations
BioSample SAMN04457957
SRA SRX1562351

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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