List of Plots/ds9 things (as I understand it)

1. do plots of the histograms (like in ZoologyInvestigations2) for the same cells for:

• chip stage(how to reprocess)
• warp stage(how to reprocess)
• g , r, i, z, y of stack stage ​http://svn.pan-starrs.ifa.hawaii.edu/trac/ipp/wiki/ZoologyInvestigations2
• SAS2.123 stacks

• expect g to be dominated the most by faint camera structures. So other bands like i or z should look more like a parabola in logy space.

2. do the histograms but mask out burntool (on stacks?)

3. do the histograms but mask out all bad (on stacks?)

4. do the density plots again (but with log colors -- ask gene how to do it easily in dvo)

5. plot the second moments xx vs yy for true and false

• expect true to be a scatter plot
• does false have any pattern?
• lots of detections have 0 moment (!?)

6. make region files for SAS2.123 (for any detections)- this will help find areas of the SAS2.123 stacks that have a lot of 'false' detections and areas that have few detections

7. do the cells with tilty streak correlated with the false detection rate? see ​http://svn.pan-starrs.ifa.hawaii.edu/trac/ipp/wiki/ZoologyInvestigations2 -- bad cells have bad false detections

8. make a list for each cell the number of false positives (are the known bad cells?)

9. investigate the false positives with the original cuts, what are they?
   • plot sloan stuff in that area
   • why were they missed? do they look like stars? do they have high proper motion? are they UFOs?

10. make region files from stripe 82 to overlay on ds9 (SAS.footprint)

11. histogram of md field (longer exposures)

12. check w band and other bands warps/stacks etc to see if it happens

13. in g and y make catalogs (no detrending) do we see stuff

14. some 3pi images do we see false detections

15. try this on a flat (all bands)

16. try on skyprobe (​http://svn.pan-starrs.ifa.hawaii.edu/trac/ipp/wiki/ZoologySkyprobe)

17. try on a dark

18. do with md (nightly, different stages)