Mercurial > repos > iuc > pysradb_search
diff test-data/test_03.tabular @ 0:1005ffbccd86 draft
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/pysradb commit 95f13fef86ee81a617814a386cb371e94cf45577
| author | iuc |
|---|---|
| date | Fri, 11 Nov 2022 07:35:39 +0000 |
| parents | |
| children |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/test-data/test_03.tabular Fri Nov 11 07:35:39 2022 +0000 @@ -0,0 +1,51 @@ +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.