Strain: C57BL6 Cervix and vagina, Female total RNA (MoCV.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 MoCV.Feml.sig23 Cell type Cervix and vagina, Female Source NHGRI RNA isolation LYNX mRNA QC passed cDNA library: Library DpnII restriction - (signature cloning using MmeI) Sequence length 20 bp MPSS: runs MoCV.Feml_sig23.5313F.f-20 1/24/2005 614465 7898 QC Passed MoCV.Feml_sig23.5313F.a-20 1/3/2005 481835 6324 QC Passed MoCV.Feml_sig23.5313W.b-20 12/24/2004 513024 9308 QC Passed MoCV.Feml_sig23.5313W.a-20 12/24/2004 479190 8670 QC Passed Run group: Total Beads successfully sequenced - 2088514 Processed Signatures - 11569