I have a data that looks like this
1:SRX000566
Submitter: WoldLab
Study: RNASeq expression profiling for ENCODE project(SRP000228)
Sample: Human cell line GM12878(SRS000567)
Instrument: Solexa 1G Genome Analyzer
Total: 4 runs, 62.7M spots, 2.1G bases
Run #1: SRR002055, 11373440 spots, 375323520 bases
Run #2: SRR002063, 22995209 spots, 758841897 bases
Run #3: SRR005091, 13934766 spots, 459847278 bases
Run #4: SRR005096, 14370900 spots, 474239700 bases
2:SRX000565
Submitter: WoldLab
Study: RNASeq expression profiling for ENCODE project(SRP000228)
Sample: Human cell line GM12878(SRS000567)
Instrument: Solexa 1G Genome Analyzer
Total: 3 runs, 51.2M spots, 1.7G bases
Run #1: SRR002052, 12607931 spots, 416061723 bases
Run #2: SRR002054, 12880281 spots, 425049273 bases
Run #3: SRR002060, 25740337 spots, 849431121 bases
3:SRX012407
Submitter: GEO
Study: GSE17153: Illumina sequencing of small RNAs from C. elegans embryos(SRP001363)
Sample: Caenorhabditis elegans(SRS006961)
Instrument: Illumina Genome Analyzer II
Total: 1 run, 3M spots, 106.8M bases
Run #1: SRR029428, 2965597 spots, 106761492 bases
Is there a compact way to convert them into tabular format (tab separated).
Hence 1 entry/row per chunk. In these case 3 rows.
I tried this but doesn't seem to work.
perl -laF/\n/ -000ne"print join chr(9),@F" myfile.txt