NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM2345165 Query DataSets for GSM2345165
Status Public on Aug 21, 2017
Title PR Uninfected Stage 1 rep 1
Sample type SRA
 
Source name Whole roots
Organisms Solanum lycopersicum; Meloidogyne incognita
Characteristics control or experimental sample: Control
tissue: roots
tomato cultivar: Pusa Ruby
tomato susceptibility to root-knot nematode infection: susceptible
days post rkn inoculation: 1,2,3 days post inoculation
disease developmental stage: No disease
Treatment protocol Five-week old tomato seedlings were inoculated with 1500 freshly hatched J2s per plant and water (control) in black potted trays. Whole roots at different days post infection (dpi) were collected with two to five technical replicates.
Growth protocol Tomato seeds were germinated in trays (36cm x 25cm x 7cm) in sterile soil:solrite (1:4) at 22±2ºC, 16h light/8h dark cycle in greenhouse chamber. Three week old seedlings were transferred to black potted trays (4cm in diameter) in soil:sand (1:1). Stocks of Meloidogyne incognita were maintained on susceptible tomato and brinjal plants in a greenhouse culture room. Infected roots were collected; egg masses were hand-dissected and kept in autoclaved double distilled water for hatching at room temperature.
Extracted molecule polyA RNA
Extraction protocol RNA extraction protocol not provided.
Transcriptome libraries were prepared using TruSeq RNA sample preparation kit v2 (Illumina, USA) according to the manufacturer’s protocol.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2000
 
Description PR_UI_123
Data processing Basecalling was performed using CASAVA version 1.8
Quality assessment was carried out using FastQC and quality filtering of raw reads was done for mean phred quality score of 20 and any contaminating adapter sequences were removed using PrinSeq and Cutadapt.
After filtering for the good quality reads, reads were aligned independently onto S. lycopersicum and M. Incognita genomes using TopHat v2.0.14 on default parameters.
After alignment, uniquely mapped reads were further quantified using HTSeq based on gene annotations.
Genome_build: S. lycopersicum genome build SL2.50; M. Incognita WB release 5 (http://parasite.wormbase.org/). The gene annotations are publicly available at: http://parasite.wormbase.org/Meloidogyne_incognita_prjea28837/Info/Index/
Supplementary_files_format_and_content: bigWig files for each sample; tab-delimited text files include read count values for each Sample.
 
Submission date Oct 14, 2016
Last update date May 15, 2019
Contact name Neha Shukla
E-mail(s) nehashukla04@gmail.com
Organization name CEITEC
Department Plant Molecular Biology
Street address Kamenice 753
City Brno
ZIP/Postal code 62500
Country Czech Republic
 
Platform ID GPL22563
Series (1)
GSE88763 Transcriptome analysis of root-knot nematode (Meloidogyne incognita)-infected tomato (Solanum lycopersicum) roots reveals complex gene expression profiles and metabolic networks of both plant and nematode during susceptible and resistance responses.
Relations
BioSample SAMN05908682
SRA SRX2245668

Supplementary file Size Download File type/resource
GSM2345165_PR_UI_123_tom_rep1.bw 133.8 Mb (ftp)(http) BW
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file
Processed data are available on Series record

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