Gd-Lysozyme: Difference between revisions
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==Unit-pixel tile positions== | ==Unit-pixel tile positions== | ||
We now know the correct detz_offset (581) and we can change the Gd-Lysozyme-t000.phil file by uncommenting the target unit cell and known setting and change the confif file to only do the indexing and integration with a detz_offset=581. | We now know the correct detz_offset (581) and we can change the Gd-Lysozyme-t000.phil file by uncommenting the target unit cell and known setting and change the confif file to only do the indexing and integration with a detz_offset=581. | ||
Now we will index the data to derive model lattices. The configuration file [[Gd-Lysozyme-27.cfg]] (for configuration run 27) names our phil parameter file [[Gd-Lysozyme-t003.phil]] (t003 means trial | Now we will index the data to derive model lattices. The configuration file [[Gd-Lysozyme-27.cfg]] (for configuration run 27) names our phil parameter file [[Gd-Lysozyme-t003.phil]] (t003 means trial 3)]. We'll then compare model and observation, from which we can deduce better metrology. This will be done for both experiments 239 and 240 separately. | ||
for m in 27 28 29 31; \ | for m in 27 28 29 31; \ | ||
do echo $m; cxi.lsf -c ~/myrelease/cxi84914/[[Gd-Lysozyme-27.cfg]] \ | do echo $m; cxi.lsf -c ~/myrelease/cxi84914/[[Gd-Lysozyme-27.cfg]] \ | ||
-o /reg/d/psdm/cxi/cxi84914/scratch/$USER/results/e239/ \ | -o /reg/d/psdm/cxi/cxi84914/scratch/$USER/results/e239/ \ | ||
-i /reg/d/psdm/cxi/cxi84914/xtc/e239 -q psanacsq -p 8 -x 239 -r ${m} -t | -i /reg/d/psdm/cxi/cxi84914/xtc/e239 -q psanacsq -p 8 -x 239 -r ${m} -t 3; done | ||
bkill 0 # stop all jobs; wrong file path | bkill 0 # stop all jobs; wrong file path |
Revision as of 18:57, 24 September 2014
In this tutorial, we assume that we are handed an SFX dataset containing Lysozyme diffraction, but are not told anything else. We will have to go through all the data runs, figure out which one is to be used for dark subtraction, and account for untrusted pixels and detector metrology. At this point, we will be prepared to integrate and merge the data. Finally, we will perform simple molecular replacement and ask whether there is any Gd signal in the anomalous difference Fourier.
Discovery of data collection parameters
Log in to pslogin.slac.stanford.edu, and then to psana. Carry through flags so that X-windows will work
ssh -YAC $USER@pslogin.slac.stanford.edu ssh -YAC psana
Go in to the working directory and source the package manager:
cd ~/myrelease sit_setup
Create a subdirectory for the 2014 tutorial files if not already done:
mkdir -p cxi84914
List out the Gd-Lysozyme XTC files (this could take time since there are many images):
ls /reg/d/psdm/cxi/cxi84914/xtc/e239 ls /reg/d/psdm/cxi/cxi84914/xtc/e240
Notice that there are numerous runs in the directory. Now we will create composite averages for each run. Grab this configuration file: mkdark_Gd-Lysozyme.cfg and put it in your cxi84914 directory. For one run only from each experiment directory:
cxi.lsf -c ~/myrelease/cxi84914/mkdark_Gd-Lysozyme.cfg \ -o /reg/d/psdm/cxi/cxi84914/scratch/$USER/initial_dark/e239/ \ -i /reg/d/psdm/cxi/cxi84914/xtc/e239 -q psanacsq -s -p 8 -x 239 -r 16 -t 0
cxi.lsf -c ~/myrelease/cxi84914/mkdark_Gd-Lysozyme.cfg \ -o /reg/d/psdm/cxi/cxi84914/scratch/$USER/initial_dark/e240/ \ -i /reg/d/psdm/cxi/cxi84914/xtc/e240 -q psanacsq -s -p 8 -x 240 -r 16 -t 0
Take note:
- -c configuration file
- -o output directory (will be created)
- -i input files (directory containing the XTC streams)
- -q which batch queue to use
- -s funnel all streams for the run into one node (takes longer, but necessary for averaging)
- -p number of cores to use on the node
- -x which experiment number
- -r which run number
- -t which processing trial (auto increments from 0 if not given)
For all the runs in the Gd-Lysozyme data set 239:
kinit aklog for m in 27 28 29 30 31; \ do echo $m; cxi.lsf -c ~/myrelease/cxi84914/mkdark_Gd-Lysozyme.cfg \ -o /reg/d/psdm/cxi/cxi84914/scratch/$USER/initial_dark/e239/ \ -i /reg/d/psdm/cxi/cxi84914/xtc/e239 -q psanacsq -s -p 8 -x 239 -r ${m} -t 0; done
For all the runs in the Gd-Lysozyme data set 240:
kinit aklog for m in 1 2 3 4 5 6 7 8 9 10 12 13 14 16 17 18 19 21 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40; \ do echo $m; cxi.lsf -c ~/myrelease/cxi84914/mkdark_Gd-Lysozyme.cfg \ -o /reg/d/psdm/cxi/cxi84914/scratch/$USER/initial_dark/e240/ \ -i /reg/d/psdm/cxi/cxi84914/xtc/e240 -q psanacsq -s -p 8 -x 240 -r ${m} -t 0; done
bjobs lists all your batch jobs; use this form for more information including other-user load:
bjobs -w -u all -q psanacsq bkill [number] # stops unwanted job
Some runs take up to 2 hrs wall time to average. Find the averages, view the max-composites, and list out header information for each experiment separately and create a table of the results:
ls /reg/d/psdm/cxi/cxi84914/scratch/$USER/initial_dark/e239/r*/000/out/*.pickle cctbx.image_viewer `find /reg/d/psdm/cxi/cxi84914/scratch/$USER/initial_dark/e239/r*/000 -name "max*.pickle"` for m in `find /reg/d/psdm/cxi/cxi84914/scratch/$USER/initial_dark/e239/r*/000 -name "max*.pickle"`; do echo $m; cxi.print_pickle $m; echo; done
Let's make a table of the results for experiment 239:
Run | Distance | Wavelength | Diffraction | Comments |
27 | 81.0 | 1.456964 | weak powder | |
28 | 81.0 | 1.456955 | strong powder | |
29 | 81.0 | 1.4569557 | strong powder | |
30 | 81.0 | 1.4569529 | dark | |
31 | 81.0 | 1.456949 | strong powder |
The next Gd-Lysozyme experiment:
ls /reg/d/psdm/cxi/cxi84914/scratch/$USER/initial_dark/e240/r*/000/out/*.pickle cctbx.image_viewer `find /reg/d/psdm/cxi/cxi84914/scratch/$USER/initial_dark/e240/r*/000 -name "max*.pickle"` for m in `find /reg/d/psdm/cxi/cxi84914/scratch/$USER/initial_dark/e240/r*/000 -name "max*.pickle"`; do echo $m; cxi.print_pickle $m; echo; done
Let's make a table of the results for experiment 240:
Run | Distance | Wavelength | Diffraction | Comments |
1 | 156.0 | 1.145418 | dark | |
2 | 101.0 | 1.454165 | strong powder | |
3 | 81.0 | 1.454175 | strong powder | |
4 | 81.0 | 1.454175 | strong powder | |
5 | 81.0 | 1.454175 | strong powder | |
6 | 81.0 | 1.454176 | strong powder | |
7 | 81.0 | 1.454176 | strong powder | |
8 | 97.735 | 1.453730 | dark | |
9 | 171.0 | 1.4569401 | weak powder | |
10 | 81.0 | 1.456952 | strong powder | |
12 | 81.0 | 1.45695 | weak powder | |
13 | 81.0 | 1.45815 | dark | |
14 | 81.0 | 1.456952 | strong powder | |
16 | 81.0 | 1.45697 | strong powder | |
17 | 81.0 | 1.457426 | weak powder | |
18 | 81.0 | 1.467101 | very weak powder | |
19 | 81.0 | 1.456950 | strong powder | |
21 | 81.0 | 1.456949 | strong powder | |
24 | 81.0 | 1.456950 | very weak powder | |
25 | 81.0 | 1.456958 | strong powder | |
26 | 81.0 | 1.4569358 | strong powder | |
27 | 81.0 | 1.4569524 | strong powder | |
28 | 81.0 | 1.456964 | very weak powder | |
29 | 81.0 | 1.4570738 | strong powder | saturated spots |
30 | 81.0 | 1.4569528 | strong powder | saturated spots |
31 | 81.0 | 1.4569488 | dark | |
32 | 81.0 | 1.456953 | strong powder | |
33 | 81.0 | 1.4569476 | strong powder | |
34 | 81.0 | 1.4569505 | strong powder | |
35 | 81.0 | 1.456966 | strong powder | |
36 | 81.0 | 1.456948 | strong powder | |
37 | 81.0 | 1.4573264 | strong powder | |
38 | 81.0 | 1.4569576 | strong powder | |
39 | 81.0 | 1.4569520 | strong powder | |
40 | 81.0 | 1.4569505 | strong powder |
Some conclusions:
- Run 30 was the dark run for experiment 239. We'll use the average and standard deviation for further processing. Tutorial students can take result from the instructor's directory:
/reg/d/psdm/cxi/cxi84914/scratch/tmmclark/initial_dark/e239/r0030/000/out/avg-r0030.pickle /reg/d/psdm/cxi/cxi84914/scratch/tmmclark/initial_dark/e239/r0030/000/out/stddev-r0030.pickle
- Runs 1, 8, 13 and 31 were dark runs for experiment 240. We will discard runs 1 and 8 since the detector distances are unique and would require separate detector calibration. Either run 13 or 31 will work so we'll use the average and standard deviation of run 31 for further processing of experiment 240. Tutorial students can take result from the instructor's directory:
/reg/d/psdm/cxi/cxi84914/scratch/tmmclark/initial_dark/e240/r0031/000/out/avg-r0031.pickle /reg/d/psdm/cxi/cxi84914/scratch/tmmclark/initial_dark/e240/r0031/000/out/stddev-r0031.pickle
- We are interested in getting the Gd anomalous signal from lysozyme, runs were collected at the far remote for f” at approximately 8500 eV or 1.457 Angstroms. See the X-ray Anomalous Scattering.
- We'll accept runs 27-29 and 31 ("calibration27") for experiment 239, and in experiment 240 runs 3-7, 10, 11, 14-19, 23-30 and 32-40 ("calibration3"). We'll also discard run 9 of experiment 240 as the diffraction was relatively weak and the unique detector distance would require separate detector calibration.
Prepare to mask out the untrusted pixels
We'll now calculate dark-subtracted averages for experiment 239.
for m in 27 28 29 31; \ do echo $m; cxi.lsf -c ~/myrelease/cxi84914/mkavg_e239.cfg \ -o /reg/d/psdm/cxi/cxi84914/scratch/$USER/averages/e239/ \ -i /reg/d/psdm/cxi/cxi84914/xtc/e239 -q psanacsq -s -p 8 -x 239 -r ${m} -t 0; done
This repeats exactly the same averaging calculations as before, except the dark average from run 30 is subtracted. The dark image to be subtracted (along with its std deviation) is defined in the configuration file mkavg_e239.cfg.
Now we'll figure out which pixels are untrusted, and thus should not be integrated. Three criteria will be used:
- Hot pixels--on the average-dark the pixel values exceed 1150 (should be fine tuned by inspecting the dark & using trial and error)
- Hot pixels--on the standard deviation-dark the stddev exceeds 4 and therefore unreliable (also should be fine tuned by trial and error)
- Cold pixels or shadows--on a maximum-composite data image, inspect values and set a minimum threshold value (we choose 15 here)
For more information on masking parameters see creating a mask image
cxi.make_mask -v --maxproj_min 15 --avg_max 1150 --stddev_max 4 --output mask_base.pickle \ /reg/d/psdm/cxi/cxi84914/scratch/$USER/initial_dark/e239/r0030/000/out/avg-r0030.pickle \ /reg/d/psdm/cxi/cxi84914/scratch/$USER/initial_dark/e239/r0030/000/out/stddev-r0030.pickle \ /reg/d/psdm/cxi/cxi84914/scratch/$USER/averages/e239/r0027/000/out/max-r0027.pickle
Inspect the mask:
cctbx.image_viewer mask_base.pickle show_untrusted=true
Non-bonded pixels are masked and untrusted regions of high and low/negative intensity.
Now We need to repeat the procedure above to calculate dark-subtracted averages for experiment 240.
for m in 3 4 5 6 7 10 12 14 16 17 18 19 21 23 24 25 26 27 28 29 20 32 33 34 35 36 37 38 39 40; \ do echo $m; cxi.lsf -c ~/myrelease/cxi84914/mkavg_e240.cfg \ -o /reg/d/psdm/cxi/cxi84914/scratch/$USER/averages/e240/ \ -i /reg/d/psdm/cxi/cxi84914/xtc/e240 -q psanacsq -s -p 8 -x 240 -r ${m} -t 0; done
This repeats exactly the same averaging calculations as before, except the dark average from run 31 is subtracted. The dark image to be subtracted (along with its std deviation) is defined in the configuration file mkavg_e240.cfg.
Now we'll figure out which pixels are untrusted, and thus should not be integrated. Three criteria will be used:
- Hot pixels--on the average-dark the pixel values exceed 1250 (should be fine tuned by inspecting the dark & using trial and error)
- Hot pixels--on the standard deviation-dark the stddev exceeds 4 and therefore unreliable (also should be fine tuned by trial and error)
- Cold pixels or shadows--on a maximum-composite data image, inspect values and set a minimum threshold value (we choose 14 here)
For more information on masking parameters see creating a mask image
cxi.make_mask -v --maxproj_min 14 --avg_max 1250 --stddev_max 4 --output mask_base.pickle \ /reg/d/psdm/cxi/cxi84914/scratch/$USER/initial_dark/e240/r0031/000/out/avg-r0031.pickle \ /reg/d/psdm/cxi/cxi84914/scratch/$USER/initial_dark/e240/r0031/000/out/stddev-r0031.pickle \ /reg/d/psdm/cxi/cxi84914/scratch/$USER/averages/e240/r0018/000/out/max-r0018.pickle
Inspect the mask:
cctbx.image_viewer mask_base.pickle show_untrusted=true
Non-bonded pixels are masked and untrusted regions of high and low/negative intensity.
Correct the detector metrology
Accurate data integration requires highly precise knowledge of pixel positions in laboratory space (metrology). Gaining this knowledge is especially difficult due to the segmented nature of the CSPAD detector, which is tiled into 64 application-specific integrated circuits (ASICs). The 64 ASICs are arranged in quadrants that are approximately 4-fold rotationally symmetric, with 8 sensors per quadrant and 2 ASICs per sensor. The sensors are field-serviceable, and may therefore change from Run to Run.
We thus need to determine positions and rotations for all 64 tiles, ideally down to an accuracy on order of 10 microns. As a general overview, cctbx takes the following steps:
- Tile placement in physical space is measured by the beamline operators optically using electron microscopy. This is done at the per-sensor level (2 ASICs per sensor). This is already hard-coded; nothing for the user to do.
- Relative positions of the quadrants are determined coarsely by considering powder rings.
- Sensor positions are refined based on Bragg spot diffraction, allowing for whole-pixel translations in x and y.
- ASIC positions are refined to subpixel accuracy based on Bragg diffraction, allow for sub-pixel translations and rotations.
Quadrant positions
The electron microscopy step above determines only the sensor positions relative to the frames of reference of each quadrant; but not the absolute position of each quadrant in space. At the CXI instrument, the forward detector DS1 has rail-mounted quadrants to allow re-sizing of the central hole. The quadrant placement should be assessed for both the forward and back (DS2) detectors.
For lysozyme we examine one of the strong images (maximum composite). Students may use the instructor's files ($USER=tmmclark). We first determine that our image has a timestamp that identifies it within cctbx as being from run 7 (2013):
cxi.print_pickle /reg/d/psdm/cxi/cxi84914/scratch/$USER/averages/e239/r0028/000/out/max-r0028.pickle > Detector format version: CXI 7.1 cxi.detector_format_versions cxi.detector_format_versions "CXI 7.1" cxi.view /reg/d/psdm/cxi/cxi84914/scratch/$USER/averages/e239/r0028/000/out/max-r0028.pickle \ distl.detector_format_version="CXI 7.1" viewer.calibrate_unitcell.d_min=10 \ viewer.calibrate_unitcell.unitcell=79,79,38,90,90,90 viewer.calibrate_unitcell.spacegroup=P43212
The "Settings" GUI panel shows detector distance as well as the hard-coded quadrant positions corresponding to "CXI 7.1", namely [2, -6, 3, -6, -7, 0, -1, -4]. Tile translations have been zeroed out in the code. The settings can be changed in the panel, or alternately given as a separate command line parameter (distl.quad_translations=2,-6,3,-6,-7,0,-1,-4). The object is to align the powder pattern with the predicted rings (red circles) based on the unit cell parameters. It can be seen that the alignment is not quite perfect.
Since we have well-formed powder rings, we can run the automatic quadrant positioning tool:
cspad.quadrants /reg/d/psdm/cxi/cxi84914/scratch/$USER/averages/e239/r0028/000/out/max-r0028.pickle \ distl.detector_format_version="CXI 7.1" > The NEW QUAD translations are: [2, -6, 4, -6, -6, 1, 0, -4]
Try a few different max-composites from runs 27, 29 and 31:
The NEW QUAD translations are: [2, -6, 4, -6, -9, 2, 0, -4] (poor self correlation value approx. 0.06 weak powder diffraction for this run)
The NEW QUAD translations are: [3, -4, 5, -6, -6, 1, 0, -4]
The NEW QUAD translations are: [2, -6, 4, -6, -6, 1, 0, -4]
These can be pasted on to the command line for graphical review:
cxi.view /reg/d/psdm/cxi/cxi84914/scratch/$USER/averages/e239/r0028/000/out/max-r0028.pickle \ distl.detector_format_version="CXI 7.1" viewer.calibrate_unitcell.d_min=10 \ viewer.calibrate_unitcell.unitcell=79,79,38,90,90,90 viewer.calibrate_unitcell.spacegroup=P43212\ distl.quad_translations=2, -6, 4, -6, -6, 1, 0, -4
This looks slightly better. From the GUI it also appears that distance=81 fits; meaning that the detz_offset for the configuration file of 571 is ok.
Now we need to check e240:
For lysozyme we examine one of the strong images (maximum composite). Students may use the instructor's files ($USER=nksauter). We first determine that our image has a timestamp that identifies it within cctbx as being from run 7 (2013):
cxi.print_pickle /reg/d/psdm/cxi/cxi84914/scratch/$USER/averages/e240/r0029/000/out/max-r0029.pickle > Detector format version: CXI 7.1 cxi.detector_format_versions cxi.detector_format_versions "CXI 7.1" cxi.view /reg/d/psdm/cxi/cxi84914/scratch/$USER/averages/e240/r0019/000/out/max-r0029.pickle \ distl.detector_format_version="CXI 7.1" viewer.calibrate_unitcell.d_min=10 \ viewer.calibrate_unitcell.unitcell=79,79,38,90,90,90 viewer.calibrate_unitcell.spacegroup=P43212
The "Settings" GUI panel shows detector distance as well as the hard-coded quadrant positions corresponding to "CXI 7.1", namely [2, -6, 3, -6, -7, 0, -1, -4]. Tile translations have been zeroed out in the code. The settings can be changed in the panel, or alternately given as a separate command line parameter (distl.quad_translations=2,-6,3,6,-7,0,-1,-4. The object is to align the powder pattern with the predicted rings (red circles) based on the unit cell parameters. It can be seen that the alignment is not quite perfect.
Since we have well-formed powder rings, we can run the automatic quadrant positioning tool:
cspad.quadrants /reg/d/psdm/cxi/cxi84914/scratch/$USER/averages/e240/r0029/000/out/max-r0029.pickle \ distl.detector_format_version="CXI 7.1" > The NEW QUAD translations are: [2, -6, 4, -6, -6, 1, 0, -4]
Try a few different max-composites from runs 3, 7, 17, 27:
The NEW QUAD translations are: [2, -5, 4, -6, -6, 1, 0, -3]
The NEW QUAD translations are: [2, -5, 4, -6, -6, 1, 0, -4]
The NEW QUAD translations are: [19, -6, 3, -6, -11, 11, 1, -1] (very poor self-correlation coefficient around 0.06 run 17 is weak powder and not a good run to use for the metrology)
The NEW QUAD translations are: [3, -4, 4, -6, -6, 1, 0, -4]
These can be pasted on to the command line for graphical review:
cxi.view /reg/d/psdm/cxi/cxi84914/scratch/$USER/averages/e240/r0029/000/out/max-r0029.pickle \ distl.detector_format_version="CXI 7.1" viewer.calibrate_unitcell.d_min=10 \ viewer.calibrate_unitcell.unitcell=79,79,38,90,90,90 viewer.calibrate_unitcell.spacegroup=P43212\ distl.quad_translations= 2, -6, 4, -6, -6, 1, 0, -4
This looks slightly better. We will continue in the next section to test the distance and find the best value.
Data Discovery Phase
Before we can move forward with metrology on the pixel and sub pixel level, we must test if the data can be indexed and index a test image. Beginning with e239 we will choose run 27 and run hit finding and dump the images for trial 0. The configuration file Gd-Lysozyme-27_discover.cfg (for configuration run 27) names our phil parameter file Gd-Lysozyme-t000.phil (t000 means trial 0)] for trial 0 we comment out the target cell and setting. Modules that are commented out in the config file can be uncommented for indexing once we discover the correct parameters.
cxi.lsf -c ~/myrelease/cxi84914/Gd-Lysozyme-27_discover.cfg \ -o /path to home/myrelease/cxi84914/e239/ \ -i /reg/d/psdm/cxi/cxi84914/xtc/e239 -q psanacsq -p 8 -x 239 -r 27 -t 0
Nothing can progress until we successfully index an image. The next steps involve adjusting the configuration file so that we can just look the images and find one that should index. First we make a new configuration file that just does a hit find and a raw image dump and examine images to find one with "good" diffraction. We choose the s00 stream as this will give a thin slice of the entire run and we can examine all images from this run using the command:
cctbx.image_viewer shot-s00-20130315225*
Looking through these images the best is the third image (shot-s00-20130315225354116.pickle). First we check using this image if spot finder has the correct parameters by using the .phil file parameters in image viewer as follows:
distl.image_viewer distl.minimum_signal_height=5 distal.minimum_spot_height=10 \ distal.minimum_spot_area=1 shot-s00-20130315225354116.pickle
The spot_finder is finding the spots correctly so it seems there is another issue. In examine the images it is clear that the water rings are not at the expected resolution of approximately 3.5 angstroms but rather around 1.8 angstroms indicating that the detz_offset is incorrect (way off) and indexing is not going to work until this is fixed.
This brings us to trial 1. The detz_offset is incorrect and we aren't in the ball park so first we will try a detz_offset = 591 which puts the detector at 100 mm away to make the water rings be closer to a 3.5 angstrom resolution. To do this we edit Gd-Lysozyme-27_discover.cfg by uncomment the indexing module (also comment out my_ana_pkg.mod_dump:img_thresh, if you don't want to dump the raw images a second time) and change detz_offset to 591. Then run the following command:
cxi.lsf -c ~/myrelease/cxi84914/Gd-Lysozyme-27_discover.cfg \ -o /reg/d/psdm/cxi/cxi84914/scratch/USERNAME/results/e239/ \ -i /reg/d/psdm/cxi/cxi84914/xtc/e239 -q psanacsq -p 8 -x 239 -r 27 -t 1
Looking at ~/myrelease/cxi84914/e239/r0027/stdout log file s00.out the unit cell found (86.3581, 86.3581, 42.8606, 90, 90, 90) is not the correct one and many images did not index at all. We need to try to get to a value for detz_offset that is in the correct range. For trial 2 we will use a detz_offset of 581, so the detz_offset in Gd-Lysozyme-27_discover.cfg is changed t0 581 and we run the following command:
cxi.lsf -c ~/myrelease/cxi84914/Gd-Lysozyme-27_discover.cfg \ -o /reg/d/psdm/cxi/cxi84914/scratch/USERNAME/results/e239/ \ -i /reg/d/psdm/cxi/cxi84914/xtc/e239 -q psanacsq -p 8 -x 239 -r 27 -t 2
Checking the log file the indexed unit cell is (78.1073, 78.1073, 39.1608, 90, 90, 90) which is much closer to what we expect and checking how many indexed images are in r0027/002/out
ls -l |wc -1
counts all files in current directory and we get 188 indexed images out of a total of 303 total images in our image dump of r0027 for trial 0. Before accepting detz_offset of 581 we will try a series of detz_offset values in the range of 575 - 595. Go to your my release in your home directory and create a new directory called diet_trials; cd into it and run this command to create new configuration files with the test detz_offset values.
for i in `seq 575 595`; do vi -c "%s/581/$i/g" -c "w Gd-Lysozyme-27_discover0$i.cfg" \ -c q\! ../cxi84914/Gd-Lysozyme-27_discover0.cfg ; done
Here, a vi command is executed repeatedly that searches for the number 581 in your config file and replaces it with a number from 575 to 595, then writes out the new file with an appropriate file name. If this seems like a poor window to search, note that the number was originally 571, and has already been optimized to 581 through earlier trials.
Next, submit indexing jobs for each candidate detz offset from your myrelease folder:
for i in `seq 575 595`; do cxi.lsf -c dist_trials/Gd-Lysozyme-27_discover0$i.cfg \ -o /reg/d/psdm/cxi/cxi84914/scratch/$USER/dist_trials/ -i /reg/d/psdm/cxi/cxi84914/xtc/e239 -r 27 -q psanacsq -p 8 -t $i; done
When complete, go to your results directory:
cd /reg/d/psdm/cxi/cxi84914/scratch/$USER/dist_trials/r0027
Then determine which detz offset is best:
for i in `ls`; do echo -n "$i "; ls $i/out | wc -l; done
Output:
575 80 576 98 577 120 578 153 579 182 580 185 581 187 582 159 583 154 584 142 585 120 586 116 587 103 588 85 589 81 590 68 591 64 592 58 593 60 594 53 595 50
The detz_offset of 581 gives the most indexed images. So now we move to the next step in the metrology (unit-pixel tile positions).
Unit-pixel tile positions
We now know the correct detz_offset (581) and we can change the Gd-Lysozyme-t000.phil file by uncommenting the target unit cell and known setting and change the confif file to only do the indexing and integration with a detz_offset=581. Now we will index the data to derive model lattices. The configuration file Gd-Lysozyme-27.cfg (for configuration run 27) names our phil parameter file Gd-Lysozyme-t003.phil (t003 means trial 3)]. We'll then compare model and observation, from which we can deduce better metrology. This will be done for both experiments 239 and 240 separately.
for m in 27 28 29 31; \ do echo $m; cxi.lsf -c ~/myrelease/cxi84914/Gd-Lysozyme-27.cfg \ -o /reg/d/psdm/cxi/cxi84914/scratch/$USER/results/e239/ \ -i /reg/d/psdm/cxi/cxi84914/xtc/e239 -q psanacsq -p 8 -x 239 -r ${m} -t 3; done
bkill 0 # stop all jobs; wrong file path
A quick command to count how many integration files there are:
for m in `seq 27 31`; \ do echo $m `find /reg/d/psdm/cxi/cxi84914/scratch/$USER/results/e239/r00$m/000/integration \ -name "int*.pickle"|wc -l` ; done; \ find /reg/d/psdm/cxi/cxi84914/scratch/$USER/results/e239/*/000/integration -name "int*.pickle"|wc -l
Determine whole-pixel translations for all sensors on the CSPAD.
cspad.metrology data=/reg/d/psdm/cxi/cxi84914/scratch/$USER/results/e239/r*/000/integration \ bravais_setting_id=9 max_frames=1000 min_count=25 \ detector_format_version="CXI 7.1" /reg/neh/home/$USER/myrelease/cxi84914/ \ Gd-Lysozyme-t000.phil | tee Gd-27-t000.unit
List out the new unit translations:
cat Gd-27-t000.unit |grep -A21 "Unit translations"
Results from three refinement cycles are listed; capture the last one and incorporate it into a new version of the integration phil file, L498-thermolysin-t001.phil. Also in this phil file, for the next integration round we'll increase our integration limits (3 places) to 1.8 Angstroms. After editing the configuration file to use this new phil file, submit the new round of integration jobs.
For the purpose of the tutorial, we'll drop runs 17-20 since they contribute only 1095 lattices compared with >18000 for runs 21-27. Fine-tuning of the metrology for runs 17-20 would have to be performed separately since the detector is at a different distance.
for m in 21 22 23 24 25 26 27; \ do echo $m; cxi.lsf -c ~/myrelease/cxi84914/L498-thermolysin-21.cfg \ -o /reg/d/psdm/cxi/cxi84914/scratch/$USER/results/e157/ \ -i /reg/d/psdm/cxi/cxi84914/xtc/e157 -q psanacsq -p 8 -x 157 -r ${m} -t 1; done
Another round of metrology refinement, this time using trial 001 as the basis:
cspad.metrology data=/reg/d/psdm/cxi/cxi84914/scratch/$USER/results/e157/r002[1-7]/001/integration bravais_setting_id=12 max_frames=1000 min_count=25 detector_format_version="CXI 5.1" cxi84914/L498-thermolysin-t001.phil | tee L498-21-t001.unit
…proving we have not yet converged. Take this output and construct trial 002: L498-thermolysin-t002.phil; edit the *.cfg file. Submit another round of integration jobs:
for m in 21 22 23 24 25 26 27; \ do echo $m; cxi.lsf -c ~/myrelease/cxi84914/L498-thermolysin-21.cfg \ -o /reg/d/psdm/cxi/cxi84914/scratch/$USER/results/e157/ \ -i /reg/d/psdm/cxi/cxi84914/xtc/e157 -q psanacsq -p 8 -x 157 -r ${m} -t 2; done
Evaluate metrology again:
cspad.metrology data=/reg/d/psdm/cxi/cxi84914/scratch/$USER/results/e157/r002[1-7]/002/integration bravais_setting_id=12 max_frames=1500 min_count=25 detector_format_version="CXI 5.1" cxi84914/L498-thermolysin-t002.phil | tee L498-21-t002.unit
Add sub-pixel corrections
There are negligible changes in the unit-translations (non-zero only at large radius), and the rmsd is now 0.96 pixels. We'll leave the unit-translations exactly where they are now, and add subpixel translations and rotations to the phil file. These are taken from the very end of the log file (L498-21-t002.unit). Incorporate these into L498-thermolysin-t003.phil.
Integrate the data
We're ready for the final integration trial, which will be t003. Again edit the configuration file Gd-thermolysin-27.cfg so that it points to the latest phil file, L498-thermolysin-t003.phil. Submit integration jobs:
for m in 27 28 29 31; \ do echo $m; cxi.lsf -c ~/myrelease/cxi84914/L498-thermolysin-27.cfg \ -o /reg/d/psdm/cxi/cxi84914/scratch/$USER/results/e157/ \ -i /reg/d/psdm/cxi/cxi84914/xtc/e157 -q psanacsq -p 8 -x 157 -r ${m} -t 3; done
…19980 lattices indexed and integrated. If the second lattice is desired (about 10% of images have two) set indexing.outlier_detection.switch=True in the phil file, and integrate again under a new trial number (-t 4).
Trial 005: Try first-lattice again, correcting an omission of the mask_pixel_value=-2 phil parameter in trial 003.
…19987 lattices indexed and integrated in trial 005.
Merge the data
on pslogin, download the reference structure 2tli from the pdb (must be done on pslogin, the only outward-facing host). 2tli.pdb will be used for per-image scaling; 2tli.mtz will be used for reporting correlation to isomorphous synchrotron data.
phenix.fetch_pdb --mtz 2tli
back to psana. Get the command file mergethermo.csh.
mkdir /reg/d/psdm/cxi/cxi84914/scratch/$USER/merge/e157 cd /reg/d/psdm/cxi/cxi84914/scratch/$USER/merge/e157 ./mergethermo.csh
Better log file from trial 005--using untrusted pixel mask
Solve the structure
Some quick commands to evaluate the data. Here the result *.mtz files must be moved back to your $HOME directory and transferred to your laptop to run PHENIX:
cp /reg/d/psdm/cxi/cxi84914/scratch/$USER/merge/e157/thermoanom_2tli_s0_mark0.mtz $HOME cp /reg/d/psdm/cxi/cxi84914/scratch/$USER/merge/e157/thermonoanom_2tli_s0_mark0.mtz $HOME
Always use the "s0" files; "s1" and "s2" are the semi-datasets used only to calculate CC1/2.
phenix.fetch_pdb --mtz 2tli phenix.xtriage thermonoanom_2tli_s0_mark0.mtz scaling.input.xray_data.obs_labels=Iobs > triage_noanom.log
Wilson B factor:14.8
phenix.automr 2tli.pdb thermonoanom_2tli_s0_mark0.mtz seq_file=2tli.fa identity=100 copies=1 build=False
The MR-placed model is in ./AutoMR_run_1_/MR.1.pdb.
Obtain the set of R-free-flags used in the Nature Methods paper
wget http://cci.lbl.gov/publications/download/4ow3_original_iobs_flags.mtz
Refine the model
phenix.refine ./AutoMR_run_1_/MR.1.pdb refinement.output.prefix=001 \ xray_data.file_name=thermonoanom_2tli_s0_mark0.mtz \ xray_data.r_free_flags.file_name=4ow3_original_iobs_flags.mtz \ xray_data.r_free_flags.label=R-free-flags \ main.number_of_macro_cycles=6 optimize_xyz_weight=True \ optimize_adp_weight=True nproc=20 refinement.input.xray_data.labels=IMEAN \ ordered_solvent=true ordered_solvent.mode=every_macro_cycle
trial 003: RWORK = 23.1% RFREE = 26.5% out to 2.1 Angstrom
trial 005: RWORK = 22.0% RFREE = 26.3% out to 2.1 Angstrom (taking untrusted pixels into account)
Run an ersatz script (provided by Nat Echols) to measure the peak heights of the anomalous scatterers.
libtbx.python map_height_at_atoms.py \ 001_001.pdb thermoanom_2tli_s0_mark0.mtz \ input.xray_data.labels=Iobs \ xray_data.r_free_flags.file_name=4ow3_original_iobs_flags.mtz \ xray_data.r_free_flags.label=R-free-flags
Promising results for the Zn and one Ca:
pdb="ZN ZN A 317 " : 5.97 sigma pdb="CA CA A 318 " : 0.93 sigma pdb="CA CA A 319 " : 2.74 sigma pdb="CA CA A 320 " : 1.08 sigma pdb="CA CA A 321 " : 0.20 sigma
Better results from trial 005:
pdb="ZN ZN A 317 " : 7.66 sigma pdb="CA CA A 318 " : 1.10 sigma pdb="CA CA A 319 " : 2.52 sigma pdb="CA CA A 320 " : 1.40 sigma pdb="CA CA A 321 " : 1.01 sigma