Strain: C57BL6 Kidney:cortex, Female total RNA (MoKi.FeCr) received from National Human Genome Research Institute was analyzed through Bioanalyzer and passed our quality control test. The mRNA was processed according to the MPSS protocol as outlined in the previous publications (Brenner, S., et al. (2000) Proc Natl Acad Sci U S A 97(4): 1665-1670 and Brenner, S. et al., Nat. Biotechnol 18(6): 630-634). Briefly, the mRNA was reverse transcribed and the cDNA was digested with Dpn II. The 20 bases adjacent to the 3? most Dpn II site was cloned into a Megaclone vector. The resulting library was amplified and loaded onto microbeads. About 1.6 million microbeads were loaded into each flow cell and the signature sequences were determined by a series of enzymatic reactions as outlined in the above publications. The abundance for each signature was converted to transcripts per million (tpm) for the purpose of comparisons between samples. Cells/tissue: Library MoKi.FeCr.sig23 Cell type Kidney:cortex, Female Source NHGRI RNA isolation LYNX mRNA QC passed cDNA library: Library DpnII restriction - (signature cloning using MmeI) Sequence length 20 bp MPSS: runs MoKi.FeCr_sig23.5127F.d-20 10/26/2004 399871 7014 QC Passed MoKi.FeCr_sig23.5127F.b-20 10/4/2004 312111 7330 QC Passed MoKi.FeCr_sig23.5127F.a-20 10/2/2004 326199 7481 QC Passed MoKi.FeCr_sig23.5127W.c-20 8/16/2004 677674 11364 QC Passed MoKi.FeCr_sig23.5127W.a-20 8/10/2004 662486 10215 QC Passed Run group: Total Beads successfully sequenced - 2378341 Processed Signatures - 13475
