Moore Notes 3 16 15
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Group Call
- Participants: Katie, Tom, Patrick, Stephen, Ladan, Josh, Sarah
- Tara Oceans analysis:
- Running samples (Stephen)
- Stephen found a bug in rapsearch (authors looking into it)
- Tom will conduct a run with old version and shotmap batching
- Filter sizes (Josh)
- Five different sizes (overlapping)
- Most sizes not done at most geographic locations (example)
- Size 0.22 to 3.0 is most common, 0.22 to 1.6 used in other locations
- Confounded with location, so cannot model out
- Stephen: filter size is positively correlated with average genome size
- Josh will spot check for any missing files and summarize
- Powers et al. (2015) natural products paper http://elifesciences.org/content/4/e05048
- Used eSNaPD: http://esnapd2.rockefeller.edu
- Patrick: coverage may be lower in non-targeted Tara Oceans data
- Tom: disentangling taxonomic signal would be a good idea
- Tom: look at hits on a gene family phylogeny
- Josh: places with highest level (>1% of reads) of each gene family cluster
- But should not be called "hotspots" since only at sample locations and not global
- Survey gap analysis: predicting where to sample to find different functions from previously known
- Which protein families and marine systems to focus on?
- Quorum sensing (too diverse?)
- KS domains good because same domain used for many different functions
- Non-ribosomal peptide synthesis
- Peter Dornstein: mass spec database (BLAST for peak profiles) to prioritize
- Running samples (Stephen)
- Next calls
- March 30: Patrick
- April 13: Tara Oceans and Sharpton lab clade diversity project