Working Group 3 - Motifs and conservation
From Wiki
Jump to navigationJump to search
Ab-initio motif finding methods (Vlad, Yulia, others)
- Optimizing existing motif
- Finding novel motifs
ChIP-Seq and motif finding
- Motif finding using ChIP-Seq data, or
- Use ChIP-Seq to validate novel TF binding motifs
- TF knockdown CAGE (Morana)
Exo-ChIP gives super-nice motifs (Ben Brown)
Deorphanize TFs
- Ranked list of candidate novel motifs for orphan TFs
- Promoters expressed in a sample → novel motifs → TFs expressed in that sample
- Use motif activity to reduce the number of motifs to look for
- Existing literature in this area?
Distinguish true promoters from other CAGE data
- Timo’s approach
TFBS clusters; combinations of TFs binding near each other
CAGE promoter shapes can be associated with specific motifs
How to use epigenetic data in motif finding
- Cell-type/condition specific
- Narrow the motif search space promoter-by-promoter
Non-TF motif finding
- CAGE signal in the 3’ UTR
- miRNA binding sites in 3’ UTRs
- RNAseq, CAGEscan, RACE to find the extent of the transcript
- motif activity – type calculations applied to miRNAs
Data exchange, mailing list, wiki
- Heated discussions on the mailing lists are encouraged
- Wiki can contain data, detailed descriptions of the methodology
Upload prediction tracks to Zenbu to make them viewable to everybody
- In addition to flat-files on the Wiki
State-specific motifs:
- Ranked list of motifs specific / enriched in specific samples