317.576 A?
Long unit cell axis , did you align this with the rotation axis? See
https://mol-xray.princeton.edu/xray0/long_axis.html
> On Apr 16, 2025, at 10:13 PM, Stefan Clarke wrote:
>
> [External email - use caution]
>
>
> Dear CCP4 Community,
>
> I was hoping for some insight into a problem
a better spot to collect data.
> Or 'grow a better crystal'.
>
> raising the crystals and struggle is on the peak...
>
There are a number of ccp4bb postings about crystal reproducibility or crystal
diffraction improvement. Search the archives for these.
F
-
Francis E. Reyes PhD
215 UCB
University of Colorado at Boulder
rching' for a better spot to collect data.
Or 'grow a better crystal'.
F
-
Francis E. Reyes PhD
215 UCB
University of Colorado at Boulder
Julian, King of Lemurs
---------
Francis E. Reyes PhD
215 UCB
University of Colorado at Boulder
Graeme and Bob,
Wow... It's great to learn from actual experiences.
Thanks much for this write up.
If this were stackoverflow, +1.
F
On May 8, 2013, at 12:32 AM, Graeme Winter wrote:
> A couple of extra comments on top of Bob's rather comprehensive
> recommendations, based purely on a
sig.=4.4
-----
Francis E. Reyes PhD
215 UCB
University of Colorado at Boulder
Ok, I'll bite.
"I dare anyone who considers themself an expert macromolecular crystallographer
to find a way to build out of this map."
I put emphasis on "this map".
"Short of actually cheating (see below), there doesn't seem to be any automated
way to arrive at a solved structure from these
0850 USA
> phone: (240) 314-6478
> fax: (240) 314-6225
> email: swals...@umd.edu
>
> On Dec 12, 2012, at 2:55 PM, Francis E Reyes wrote:
>
>> I've had good experience with GETAX if you have a self rotation peak.
>>
>> Be careful about moving the NCS opera
S operators from
> one program to another).
>
> Thanks for your help,
>
> Nicolas
---------
Francis E. Reyes PhD
215 UCB
University of Colorado at Boulder
;> Congrats to the protein structure community.
>>
>>
>>
>> toufic el arnaout
-
Francis E. Reyes PhD
215 UCB
University of Colorado at Boulder
Hi Randy
When you say "carried along" are you saying that they are used as part of the
molecular replacement search? Or are they temporarily put aside and them simply
added to the PDB in frame with the molecular replacement solution (but are not
part of the weighted structure factors output in
[1] In addition to using lower resolution data, you should check a variety of
RMSDs as well. In fact constructing an RMSD / high resolution contour plot
would be beneficial to determine the optimum set of parameters. (That is if
you're using PHASER).
[2] You say you suspect two molecules per
ther. Both crystals have one domain that is the same in each. We'd
> like the average the one domain between the crystals, but leave the other
> domains unaveraged.
>
> How do we describe that to dmmulti?
> thanks,
> Dave
>
> --
----------
With DM errors, it would be best to supply the input you used for DM as well as
DM's complete error output.
On Sep 2, 2012, at 9:59 PM, Sofia Caria wrote:
> Dear all,
>
> Recently I have been playing with some twinned data (Britton alpha 0.447).
> Phasing was done by MR and since I have
Some people might squawk at 2MB attachments on a BB...
But that made my day..
Thanks!
On Aug 3, 2012, at 6:01 AM, Laurie Betts wrote:
> I couldn't resist this shot. It might not make the cut.but
>
>
Anyone know of a util that'll add hydrogens in a naming scheme consistent with
CNS? (reduce doesn't do this).
Thanks!
F
-----
Francis E. Reyes PhD
215 UCB
University of Colorado at Boulder
> Cheers,
>
> Jason.
>
> --
> Jason Busby
> PhD Student
> Laboratory of Structural Biology
> School of Biological Sciences
> University of Auckland
> Thomas Building 110
> 3a Symonds St
> Private Bag 92019
> Auckland 1142
> New Zealand
>
> ph:
ymonds St
> Private Bag 92019
> Auckland 1142
> New Zealand
>
> ph: +64 9 3737599 ext 84155
> fx: +64 9 3737414
>
-
Francis E. Reyes PhD
215 UCB
University of Colorado at Boulder
Do you have crystals?
Do they diffract? If so, to what resolution?
What resolution do you require to answer your biological question?
F
On Jun 12, 2012, at 7:46 PM, LISA wrote:
> Hi all,
>
> My work is to solve huge complex containing 4 different proteins and total
> molecular weight is ab
For the RNA I recommend Eric Westhof's Assemble.
F
On May 23, 2012, at 9:32 AM, jens j birktoft wrote:
> Hi everybody,
>
> Does anyone know of a (non-commercial) software that are suitable for
> modeling DNA/RNA structures. Coot is great, however I am looking something
> that allows more f
P21.. You sure about this space group? (very high confidences for space group
and laue group in pointless?)
F
On Apr 19, 2012, at 12:20 AM, LISA wrote:
> Hi all,
>
> I am trying to solve one structure by molecular replacement with phaser in
> CCP4. This a complex of a multi-domain domains
A weighted 2Fo-Fc map (which I believe is the default for most
crystallographic refinement packages).
F
---------
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
this region because of disorder or bad model
phases?
Would love people's thoughts on this one,
F
-
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
It seems that deposition of map coefficients is a good idea. Does someone have
an mtz2cif that can handle this?
Thanks!
F
-
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
I'm now preparing for the flood of 'unsubscribe ccp4bb' requests
On Apr 2, 2012, at 9:15 AM, Bernhard Rupp (Hofkristallrat a.D.) wrote:
> Guys,
>
> http://www.youtube.com/watch?v=CobZuaPMQHw
>
> second 9 in this 22 sec video
>
>
> -Original Message-
> From: CCP4 bulletin boa
he anomalous signal if heavy atom is there?
>
> thanks in advance for help and suggestions..
>
>
>
>
>
> regards
>
> Shanti Pal Gangwar
>
>
>
>
-
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
o missing large number of reflections.
Perhaps a screen shot of one of the images where this is happening would be
helpful. So we can judge the quality of the diffraction / whether the space
group is correct, etc.
F
---------
Francis E. Reyes M.Sc.
215 UCB
http://skuld.bmsc.washington.edu/scatter/AS_form.html
Maybe useful to you.
However, I would advise to do a fluorescence scan over the range given in the
graph and then use chooch to provide the precise energies for your peak and
inflection.
If you have a large crystal don't expose all of it
e. I also see lot of
>> unanswerable density in the map where lot of waters were placed. Model fits
>> to the map like a low resolution data with most of side chains don't have
>> best density.
>>
>> I was not expecting such a sudden drop in the R/Rfree and
d crystals in the same drop.
>
> Thanks for any input.
-------------
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
ize the lack of peaks on the self rotation maps).
Any help would be appreciated.
F
-------------
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
t; You could sign your own software
> (for free) and then distribute your public key to the community, in case
> you want to do something similar.
[FUD] OS X won't trust those keys, only the ones that come from apple [/FUD]
F
---------
Francis E
D/year). Or the user can go rogue
and 'Ctrl-Click' install any application.
http://www.apple.com/macosx/mountain-lion/security.html
Personally I'll probably choose Mac App Store and identified developers. (I
imagine this will be the default).
-----
Acta Cryst. (1997). D53, 734-737[ doi:10.1107/S0907444997007233 ]
The Ultimate Wavelength for Protein Crystallography?
I. Polikarpov, A. Teplyakov and G. Oliva
http://scripts.iucr.org/cgi-bin/paper?gr0657
may give some insights.
To the OP, have you solved the structure? In some cases, s
ooks so nice. To be disappointed by big
> crystals is often not a surprise to me and if you have not tried small
> crystals from the same batch well then you missed 50% of your chances to
> solve s structure with the first light the crystals saw.
>
> Jürgen
>
>
-
e cracked crystals diffract? Do you see the analogue?
F
-----
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
ed to be the protein with mass spec.
>
> Any suggestions to improve diffraction would be welcome.
>
> Thanking you in advance.
>
> Theresa
---------
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
08889), and/or its affiliates Direct contact information
>> for affiliates is available at
>> http://www.merck.com/contact/contacts.html) that may be confidential,
>> proprietary copyrighted and/or legally privileged. It is intended solely
>> for the use of the individual or entity named on this message. If you are
>> not the intended recipient, and have received this message in error,
>> please notify us immediately by reply e-mail and then delete it from
>> your system.
>>
>>
>>
>> --
>>
>> ARKA CHAKRABORTY
>> CAS in Crystallography and Biophysics
>> University of Madras
>> Chennai,India
>>
>
>
>
>
> --
>
> ARKA CHAKRABORTY
> CAS in Crystallography and Biophysics
> University of Madras
> Chennai,India
>
-
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
AD/SAD nomenclature I favor explicitly stating whether
dispersive/anomalous/isomorphous differences (and what heavy atoms for each )
were used in phasing. Aren't analyzing the differences (independent of
source) the important bit anyway?
F
-
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
dide) for 5-10 seconds and collect the anomalous
signal at home. If it kills your crystals, move to more toxic things...
>
> Thanks in advance,
>
> Federica
>
Cheers,
F
-
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
ting at low resolutions is another.
>
> Thanks for pointing this out to me - I'll have to check out the details of
> how phenix handles it, and give it a try.
>
> Pete
-
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
and processing" in Warwick there will be live streaming. This is
>> at the link http://extrplay.dl.ac.uk/ kicking off with the what's new session
>> at 9:00am GMT. The main event starts at 11:00am GMT.
>>
>> The full program is at
>> http://www.cse.scitech.
On the other hand, shooting a lower resolution crystal may get you the
conformation of the disordered domain.
Surprising at first thought, but was true in p97/VCP from the Brunger Lab.
F
On Dec 7, 2011, at 11:47 PM, atul kumar wrote:
> Dear all
>
> I have crytals which diffract up
re is a binding, but when i take the same thing
> to set drops, only DNA crystals. Kindly suggest me, what could be done.
>
>
> Thanks & Regards,
> Umar Farook.S
-----
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
e a hypothesis that the true symmetry is different. I could
> test my hypothesis by reprocessing the data were it available.
and thank you for providing yours .
F
-------------
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
est not everyone
> is really on board. Again, I am sure this has to be done, but consensus
> in this area is equally important.
-------------
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
data for improvement of a group
II intron structure. Acta Crystallogr D Biol Crystallogr (2010) vol. 66 (Pt 9)
pp. 988-1000
F
-
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
ation but could be a good starting point.
>
> Determining the transformation may be tricker - I'd try placing pseudo-atoms
> at similar features in both maps and using lsqkab to get the transformation
> matrix; but this approach would probably need tuning to get a good alignment.
&
there some formatting error I'm not seeing?
Thanks!
F
-
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
t for the solvent mask for the
other? How's this done? (a direct input of the better xtal1 mask to xtal 2
gives 'inconsistent cell info').
Thanks!
F
-------------
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
messy density maps.
F
-
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
ed by some algorithm by those programs during integration, or is it up to
the scaling/merging (by SCALA for example) step to deal with them?
Thanks!
F
<>
---------
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
I already started with an ellipse... should I extend with a rectangle down the
shaft of the beamstop?(this is FRAME.cbf after integration)
<>
Thanks!
F
-
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
ime will tell if the
drives in 2010 were any better than then drives from 2007. I doubt it though.
F
-------------
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
lliam Scott wrote:
> she asked were a few questions about a specific computer (HP Z210 8 GB with
> a low end Quadro Nvidia 400 512 MB) running "any Linux", and a specific
> computer (IMAC 4 GB 2.5 GHz with AMD Radeon HD 6750M 512 MB)
----------
but rather you want to use it as a tool
to verify the location of a ligand binding site.
Thanks!
F
-----
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
ustified residue names, however pdb may use
> only one of them.
---------
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
d profound brain things inside my head,
> I have decided to thank you for bringing peace to our home.
>Julian, King of Lemurs
-
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
chains/tails. You do this and subsequent refinement still does not produce the
expected density for the chains.
or
[3] Your solution here.
If this situation has been discussed before, please let me know .
F
---------
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
ng a rigid body or very restrained (
secondary structure | reference structure | etc ) refinement of the coordinates
for helping the fit.
Thanks!
F
-----
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
the names are not compatible. I'm trying to build an RNA
> molecule by the way.
>
> Any suggestions?
>
> Eric
---------
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
s!
F
-
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
Depending on the corectness of the (experimental or model) phases, I've seen
Co at the Ir peak and Ir at the Co peak. Use both to cross validate your model
(when you get to it) and calculate experimental phases using both (dual SAD or
2wl MAD for each heavy atom).
So no it's not
scala to scale) ?
Am I interpreting this correctly?
Thanks!
F
-
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
them to be black on the
walls. I'm looking for a supplier / catalog number of such plates.
To save bb spam, I'll take replies privately.
Thanks!
F
-----
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
Never had problems with evaporation (and this is in the relatively dry
climate of Denver, CO, especially in the winter when the relative
humidity is in the low 20%).
Using the Thermo Scientific Nanodrop 2000c.
We use it also as a prerequisite for ITC, which can be very sensitive
to proper
e resolution of the data is about 3.1A).
The unit cell is:
142.0500 142.0500 137.9200 90. 90. 120.
P6422.
Any ideas appreciated,
Thanks!
F
-------------
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
Can someone return their full path of the location of multilog (used
for browsing dmmulti output)?
I can't find it in my ccp4-6.1.13 installed from Mr Scott's distrib.
Thanks!
F
-----
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
cific position with respect to your protein.
F
-
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
age or documentation that explains
how 'Scor' is computed?
[2] Based on the results above, it seems that P 21 21 21 is the
correct s.g.?
[3] Why the failure?
Thanks!
F
-------------
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at B
at am I doing wrong? Please help me with
suggestions
Many thanks
Careina
-
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
gpg --keyserver pgp.mit.edu --recv-keys 67BA8D5D
8AE2 F2F4 90F7 9640 28BC 686F 78FD 6669 67BA 8D5D
before)
F
---------
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
gpg --keyserver pgp.mit.edu --recv-keys 67BA8D5D
8AE2 F2F4 90F7 9640 28BC 686F 78FD 6669 67BA 8D5D
Hi all
Is there a walkthru/tutorial for processing inverse beam images with
imosflm/scala? Googling a few things didn't get me anywhere.
Thanks!
F
-
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
gpg --keyserver pgp.mi
on as it's available. Our apologies for the
inconvenience.
Best wishes,
Ronan
Ronan Keegan
CCP4 Group
---------
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
gpg --keyserver pgp.mit.edu --recv-keys 67BA8D5D
8AE2 F2F4 90F7 9640 28BC 686F 78FD 6669 67BA 8D5D
delling it with water refines perfectly with
no indication of positive difference density even at 2.0 sigma cut
off. Should I modelled this density as water or as Mg2+. Your
opinions are appreciated.
JL
-------------
Francis E. Reyes M.Sc.
215 UCB
University
ingen Biomolecular Sciences and Biotechnology Institute
& Zernike Institute for Advanced Materials
University of Groningen
Nijenborgh 4, 9747 AG
Groningen, The Netherlands
-----
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
gpg --keyserver
:)
F
-
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
gpg --keyserver pgp.mit.edu --recv-keys 67BA8D5D
8AE2 F2F4 90F7 9640 28BC 686F 78FD 6669 67BA 8D5D
Oops
It pays to view the pdbset log as it gives the right matrix.
F
On Dec 1, 2010, at 10:41 AM, Francis E Reyes wrote:
Hi all
I'm trying to figure out rotation matricies for ncs averaging in DM.
Except the conventions have got me confused.
The following input script for p
.4462 -
-0.1051 -0.9808 0.1642
shift -
invert -
-108.0451 47.655 -17.5654
end
Can someone supply me with the correct matrix to input into DM (and
what convention it is?)
Thanks
F
-
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
CCP4'ers,
Are 9 datasets the maximum for an mtz file? or a single run of cad?
The manual (http://www.ccp4.ac.uk/html/cad.html) seems to suggest that
9 is the limit per cad run but not for a given mtz.
F
-
Francis E. Reyes M.Sc.
21
Hi all
Are there any online/offline 3D crystal lattice builders to explore
symmetry relationships in the unit cell given say a space group and
unit cell parameters? I need one for an educational opportunity.
Thanks!
F
-
Francis E. Reyes M.Sc
re heating than one backsoaked.
Thanks
F
-------------
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
gpg --keyserver pgp.mit.edu --recv-keys 67BA8D5D
8AE2 F2F4 90F7 9640 28BC 686F 78FD 6669 67BA 8D5D
c=144, alpha=119, beta=119, gamma=90),
-
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
gpg --keyserver pgp.mit.edu --recv-keys 67BA8D5D
8AE2 F2F4 90F7 9640 28BC 686F 78FD 6669 67BA 8D5D
Hi all
I'm interested in the scenario where crystals were screened at home
and gave lousy (say < 8-10A) but when illuminated with synchrotron
radiation gave reasonable diffraction ( > 3A) ? Why the discrepancy?
Thanks
F
---------
Francis E.
d you
never are able to completely get rid of Y. How does this affect the
analysis of determining the derivative's affinity by ITC?
References or personal experience is appreciated!
F
-----
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Bo
to be able to accommodate 35 cm (wide) by 26-30cm (height) plates.
Please reply privately.
F
-
Francis E. Reyes M.Sc.
215 UCB
University of Colorado at Boulder
gpg --keyserver pgp.mit.edu --recv-keys 67BA8D5D
8AE2 F2F4 90F7 9640 28BC 686F 78FD 6669 67BA 8D5D
Sorry a late comer to this thread but the OP mentioned "tweaking the
error model" in HKL2000. I have heard this before.What's the validity
in this? Does it actually help or does it only help the integration
numbers but you'll pay for it during refinement?
FR
On Jun 23, 2010, at 8:25 AM, "Zh
Hi all
I've been playing around with charge flipping for macromolecular
substructure determination with pretty promising results. I'm
particularly attracted to the fact that it solves structures in P1,
with no space group assumptions and curious how it would handle some
of the pseudosymme
Hi all
I'd like to add a phase error to my PHIB's and FOM's (experimental phases) that
increases linearly with higher resolution.. it's akin to taking good phases and
making them bad. Any approaches on how this can be done?
Thanks
FR
-
Francis Reyes M
Hi all
I have a solved structure that crystallizes as a trimer to a reasonable
R/Rfree, but I'm trying to rationalize the peaks in my self rotation. The space
group is P212121, calculating my self rotations from 50-3A, integration radius
of 22 (the radius of my molecule is about 44). I can see
Is this a cause for concern? FOM's are over 0.5 and Phasing Power is over 2.0.
Thanks
FR
-
Francis Reyes M.Sc.
215 UCB
University of Colorado at Boulder
gpg --keyserver pgp.mit.edu --recv-keys 67BA8D5D
8AE2 F2F4 90F7 9640 28BC 686F 78FD 6669 67BA 8D5
Hi all
I'm in search of literature *detailing* low resolution [4-5A] phasing
protocols. Heck I'll take detailed thesis chapters (since they tend to be more
detailed than pubs anyway). If you ribosome people are on this board I'd love
to hear from you.
[sarcasm]Searching for 'grasping at stra
I like the fact that MVE's plastic shipping cases have a round top, so
Fedex can't ship the container upside down.
However, I like Taylor-Wharton's wide mouth 91mm (CXR100) vs MVE's
70mm(SC 4/2V). Unfortunately Taylor-Wharton's recommended shippers
are square and could be sent upside down.
Hi All
I'm having trouble with the following ...
title [No title given]
operator -1/2*h+1/2*k-l, 1/2*h-1/2*k-l, -1/2*h-1/2*k
labin I(+)=I_Unspecified(+) SIGI(+)=SIGI_Unspecified(+)
I(-)=I_Unspecified(-) SIGI(-)=SIGI_Unspecified(-)
end
I keep getting symmetry operator error.
Thanks
FR
-
How does one calculate a simulated annealing omit map in cases of non
crystallographic symmetry? The omit map is being used to identify the
presence and configuration of a ligand and surrounding residues. The
omit region therefore will contain the ligand and residues within
hydrogen bonding
Or know of any references besides Declercq and Evrard, 2001 ? I'd love
to hear from you. Please PM me.
Cheers
FR
-
Francis Reyes M.Sc.
215 UCB
University of Colorado at Boulder
gpg --keyserver pgp.mit.edu --recv-keys 67BA8D5D
8AE2 F2F4 90F7 9640 2
+1 phenix FTW
FR
On Jan 13, 2010, at 3:28 PM, Peter Zwart wrote:
try using
phenix.reflection_file_converter data.sca
--change_of_basis="h,-k,-h-l" --sca=reindex.sca
or something like that
HTH
Peter
2010/1/13 Francis E Reyes :
Hi all
I have data integrated and scaled
Hi all
I have data integrated and scaled to P21 via denzo/scalepack. I'm concerned
about
the workflow to obtain the alternate indexing arrangement (h,k,l) ->
(h,-k,-h-l).
I was thinking .sca ( not specifying NO MERGE) -> .mtz -> reindex but the
documentation for reindex says all my DANO col
What is the space group? Is there unmodeled density? Are all residues
in your construct built? What is the refinement protocol?
FR
On Dec 18, 2009, at 6:47 AM, james09 pruza
wrote:
Dear All,
I am trying to solve a 2.55 A resolution data set. The R-factor is
around 24% while Free-R is
Hi all
I have a rotation + translation component for the 2-fold given to me
by GETAX using low resolution low quality experimental maps. I
understand that these are input into DM for NCS averaging. What are
signs of progress as well as how does one usually optimize the mask?
When doing a
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