Strain: C57BL6 Uterus, Female total RNA (MoUt.Feml) 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 MoUt.Feml.sig21 Cell type Uterus, Female Source NHGRI RNA isolation LYNX mRNA QC passed cDNA library: Library DpnII restriction - (signature cloning using MmeI) Sequence length 20 bp MPSS: runs MoUt.Feml_sig21.5159F.e-20 11/4/2004 434208 7256 QC Passed MoUt.Feml_sig21.5159F.d-20 10/29/2004 446420 7479 QC Passed MoUt.Feml_sig21.5159W.c-20 10/21/2004 352898 7078 QC Passed MoUt.Feml_sig21.5159W.a-20 9/3/2004 525703 9063 QC Passed MoUt.Feml_sig21.5159W.b-20 9/3/2004 410704 7416 QC Passed Run group: Total Beads successfully sequenced - 2169933 Processed Signatures - 12269
