comparison test-data/test_03.tabular @ 0:1005ffbccd86 draft

planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/pysradb commit 95f13fef86ee81a617814a386cb371e94cf45577

0:1005ffbccd86

run_accession	description
DRR013000	Illumina Genome Analyzer IIx sequencing; Mutation profiles in inflamed gastric epithelium with Helicobacter pylori infection during the development of gastric cancer.
DRR013001	Illumina Genome Analyzer IIx sequencing; Mutation profiles in inflamed gastric epithelium with Helicobacter pylori infection during the development of gastric cancer.
DRR013002	Illumina Genome Analyzer IIx sequencing; Mutation profiles in inflamed gastric epithelium with Helicobacter pylori infection during the development of gastric cancer.
DRR013003	Illumina Genome Analyzer IIx sequencing; Mutation profiles in inflamed gastric epithelium with Helicobacter pylori infection during the development of gastric cancer.
DRR013004	Illumina Genome Analyzer IIx sequencing; Mutation profiles in inflamed gastric epithelium with Helicobacter pylori infection during the development of gastric cancer.
DRR013005	Illumina Genome Analyzer IIx sequencing; Mutation profiles in inflamed gastric epithelium with Helicobacter pylori infection during the development of gastric cancer.
DRR013006	Illumina Genome Analyzer IIx sequencing; Mutation profiles in inflamed gastric epithelium with Helicobacter pylori infection during the development of gastric cancer.
DRR013007	Illumina Genome Analyzer IIx sequencing; Mutation profiles in inflamed gastric epithelium with Helicobacter pylori infection during the development of gastric cancer.
DRR013008	Illumina Genome Analyzer IIx sequencing; Mutation profiles in inflamed gastric epithelium with Helicobacter pylori infection during the development of gastric cancer.
DRR013009	Illumina Genome Analyzer IIx sequencing; Mutation profiles in inflamed gastric epithelium with Helicobacter pylori infection during the development of gastric cancer.
DRR013010	Illumina Genome Analyzer IIx sequencing; Mutation profiles in inflamed gastric epithelium with Helicobacter pylori infection during the development of gastric cancer.
DRR013011	Illumina Genome Analyzer IIx sequencing; Mutation profiles in inflamed gastric epithelium with Helicobacter pylori infection during the development of gastric cancer.
DRR013012	Illumina Genome Analyzer IIx sequencing; Mutation profiles in inflamed gastric epithelium with Helicobacter pylori infection during the development of gastric cancer.
DRR013013	Illumina Genome Analyzer IIx sequencing; Mutation profiles in inflamed gastric epithelium with Helicobacter pylori infection during the development of gastric cancer.
DRR013014	Illumina Genome Analyzer IIx sequencing; Mutation profiles in inflamed gastric epithelium with Helicobacter pylori infection during the development of gastric cancer.
ERR166302	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166303	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166304	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166305	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166306	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166307	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166308	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166309	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166310	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166311	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166312	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166313	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166314	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166315	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166316	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166317	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166318	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166319	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166320	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166321	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166322	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166323	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166324	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166325	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166326	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166327	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166328	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166329	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166330	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166331	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166332	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166333	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166334	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166335	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
ERR166336	Illumina Genome Analyzer II paired end sequencing; Whole exome sequencing suggests much of non BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.