NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1053022 Query DataSets for GSM1053022
Status Public on Sep 30, 2013
Title Δabpf2_48hpi reps1-3
Sample type SRA
 
Source name tissues containing both Arabidopsis thaliana plant leaves and Alternaria brassicicola fungal mycelia
Organism Alternaria brassicicola
Characteristics fungal pathogen: Alternaria brassicicola
pathogen genotype/variation: abpf2 deletion mutant
infected host plant: Arabidopsis thaliana
tissue: mixed tissues of plant leaves and fungal mycelia
developmental stage: early germination stage
time: 48hpi
Treatment protocol Arabidopsis thaliana was infected with either wild type or abpf2 deletion mutant
Growth protocol Arabidopsis thaliana (Col-0) were grown under 8/14 light and dark cycle for 5 weeks.
Extracted molecule polyA RNA
Extraction protocol Total RNA was extracted from mixed tissues of plant leaves and fungal mycelia. PolyA RNA was enriched and libraries were constructed using TruSeq RNA sample prep kit (Illumina)
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2000
 
Description enriched polyA RNA
Data processing Image analysis, base-calling, and quality checks were performed with the Illumina data analysis pipeline CASAVA v1.8.0.
The sequenced reads were mapped to the genome sequence of Al. brassicicola (version 1; http://jgi.doe.gov/Abrassicicola) and the latest genome release of Ar. thaliana (TAIR10 ) (ftp://ftp.arabidopsis.org/home/tair/Genes/) using the programs Tophat 1.3.1 (Trapnell et al., 2009) and Bowtie 0.12.7 (Langmead et al., 2009).
The program Cuffdiff version 1.0.3 (which is part of Cufflinks, (Trapnell et al., 2010)) was used to identify reads overlapping with previously predicted genes.
The expression levels of each predicted gene were determined and normalized by the mapped Fragments Per Kilobase of exon model per Million (FPKM). Differentially expressed genes between the wild type and the mutant were determined by comparing FPKM from three biological replicates for both the wild type and the mutant. We also applied a cutoff of at least a two-fold change in expression value for differential expression. The bias correction method was used while running Cuffdiff (Roberts et al., 2011).
Genome_build: genome sequence of Al. brassicicola (version 1; http://jgi.doe.gov/Abrassicicola)
Genome_build: genome release of Ar. thaliana (TAIR10 )
Supplementary_files_format_and_content: Altbr1_expression_12hpi_48hpi.txt: ProteinId, A12W (normalized expression level of gene in the wild type Alternaria), A12F2 (normalized expression level of gene in the abpf2 mutant Alternaria), A48W (normalized expression level of gene in the abpf2 mutant Alternaria), A48F2 (normalized expression level of gene in the abpf2 mutant Alternaria), PFAM annotation, GO annotation, A12W -> A12F2: Up/Down, A12W -> A12F2: q value, A12W -> A12F2: >2-fold and significant difference?, A12W -> A48W: Up/Down, A12W -> A48W: q value, A12W -> A48W: >2-fold and significant difference?, , , A12F2 -> A48F2: Up/Down, A12F2 -> A48F2: q value, A12F2 -> A48F2: >2-fold and significant difference?, A48W -> A48F2: Up/Down, A48W -> A48F2: q value, A48W -> A48F2: >2-fold and significant difference?
Supplementary_files_format_and_content: Arabidopsis_expression_12hpi_48hpi.txt: ProteinId, A12W (normalized expression level of plant gene inoculated with wild type Alternaria), A12F2 (normalized expression level of plant gene inoculated with abpf2 mutant Alternaria), A48W, A48F2, PFAM annotation, GO annotation, A12W -> A12F2: Up/Down, A12W -> A12F2: q value, A12W -> A12F2: >2-fold and significant difference?, A12W -> A48W: Up/Down, A12W -> A48W: q value, A12W -> A48W: >2-fold and significant difference?, , , A12F2 -> A48F2: Up/Down, A12F2 -> A48F2: q value, A12F2 -> A48F2: >2-fold and significant difference?, A48W -> A48F2: Up/Down, A48W -> A48F2: q value, A48W -> A48F2: >2-fold and significant difference?
 
Submission date Dec 13, 2012
Last update date May 15, 2019
Contact name Yangrae Cho
E-mail(s) yangrae@hawaii.edu
Phone 808-956-5305
Organization name University of Hawaii at Manoa
Department Plant and Environmental Protection Sciences
Street address 3190 Maile Way, St John 317
City Honolulu
State/province HI
ZIP/Postal code 96822
Country USA
 
Platform ID GPL15377
Series (1)
GSE38984 Fungal-Specific Transcription Factor AbPf2 Activates Pathogenicity in Alternaria brassicicola
Relations
SRA SRX209779
BioSample SAMN01831107

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

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap