S2R+ whole cell Untreated 886_889 smallRNA RNA-seq alignment and analysis (Celniker project, Gingeras subgroup)
Libraries were created from small RNA (less than 200nt) isolated from D. melanogaster S2R+ Whole cell Untreated cell line extracts, sequenced using Illumina GAIIx with single-end modules, and aligned with NexAlign. Tracks show read alignments and density.
The cap-enriched and 5' monophosphate D. melanogaster small RNA libraries were generated in biological duplicate. Each library was mapped independently using STAR (Gingeras Lab) to the dm3 assembly without U-extra. To further assess the data we constructed contigs from the merged biological replciates and calculated Reads per Million values for every exon annotated in Flybase 5.32 and Ginormous. Additionally, we assessed each element for reproducibility using a nonparametric irreproducible detection rate script (npIDR, Alex Dobin Gingeras lab).
Related modENCODE submissions:
Release Date: 2012-02-09