Dear phenix developers, 
    
    1) I would like to do paired refinement using the phenix refine gui.
    
    It would be nice if you could confirm if my settings are ok, or if
    there are still some settings in the background which I overlooked,
    because we see small changes in R and Rfree.
    
    a, 
    I added the model refined at higher resolution (e.g. 1.5A) and the
    mtz file cut at CC (e.g.1.5A) in the “Input data” tab, and set High
    resolution cutoff in “X-ray data and experimental phases” box to
    (e.g. 1.8A)
    
    In the refinement setting strategy tab I uncheck everything and set
    Number of cycles = 1.
    
    In “other options” I uncheck everything too.
    
    b,
    Alternatively adding a file to the input data with
    
     }
    
        xray_data {
    file_name = "/XYZ.mtz"
    labels = "FP,SIGFP"
    high_resolution = 1.8
    low_resolution = None
    outliers_rejection = True
    french_wilson_scale = True
    french_wilson {
    max_bins = 60
    min_bin_size = 40
      }
    
    refine {
    strategy = none
        sites {
    individual = None
    torsion_angles = None
    rigid_body = None
        }
    main {
    bulk_solvent_and_scale = True
    apply_overall_isotropic_scale_to_adp = True
    fix_rotamers = False
    flip_peptides = False
    nqh_flips = False
    use_molprobity = True
    simulated_annealing = False
    simulated_annealing_torsion = False
    ordered_solvent = False
    }
    
    should also do the same or have I overlooking something.
    
    2. For whatever reason I would like to do that (molprobity) - can I
    (and how can I do this)  add the command line commands also in the
    gui?
    3. In december 2012 there was a discussion about weak data and
    refinement. I would like to know if there are new data available
    showing that “Whether the benefit they describe is considered
    cosmetic or non-trivial,.....”
    4. Additionally could one short comment on what phenix is doing with
    strong (weak) reflections marked as aliens in XDS.
    
    5.
    According to the supplementary of P. Andrew Karplus, Kay Diederichs
    “Linking Crystallographic Model and Data Quality” 
    I would like to do 
    anisotropic refinement, with additional options 
    “ordered_solvent.new_solvent=anisotropic
    adp.individual.anisotropic="not element H"
    fix_rotamers=True”.
    
    Putting this in a file is enough?
    main {
    bulk_solvent_and_scale = True
    apply_overall_isotropic_scale_to_adp = True
    fix_rotamers = True
    flip_peptides = False
    nqh_flips = False
    use_molprobity = True
    simulated_annealing = False
    simulated_annealing_torsion = False
    ordered_solvent = True
    }
    refinement { 
      refine { 
        adp { 
          individual { 
            isotropic = none
            anisotropic = not element H
          } 
        } 
      } 
    } 
    
    
    The “problem” mentioned in phenix documentation is not a problem
    with the gui?
    
    it is a good idea to constantly monitor the existing solvent
    molecules and check for new ones by
    using ordered_solvent=true keyword. If it's decided to refine waters
    with anisotropic ADP then make sure that the newly added ones are
    also anisotropic;
    useordered_solvent.new_solvent=anisotropic (default is isotropic). 
    
    Thanks in advance and best regards, Georg.