Comments (5)
scholi
commented on June 11, 2024
Hi,
What is the output of
meas = Bruker(path)
meas.list_channels()
data = meas.get_channel(channel_name)from pyspm.
Wang-stables
commented on June 11, 2024
Hello,
Also have the same problem, actually I don't know how to open the .spm file with pySPM because the example show on documentation only introduce the .ita file
And for the code below:
meas = pySPM.Bruker("CaptureFile.0_00667.spm")
meas.list_channels()
the output is below:
Channels
"========"
just like above(I use quote to make the == part won't be the format as github wish)
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scholi
commented on June 11, 2024
.spm is not a Bruker file format, so you cannot use the Bruker module to load it. Unfortunately many instruments are using the spm extension: http://gwyddion.net/documentation/user-guide-en/file-formats.html
Could you tell me which one?
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Wang-stables
commented on June 11, 2024
Thank you for your asking, I'm asking others if they know the true format
is, because I can't sure about this.
Olivier Scholder ***@***.***> 於 2023年3月6日 週一 上午5:44寫道：
… .spm is not a Bruker file format, so you cannot use the Bruker module to
load it. Unfortunately many instruments are using the spm extension:
http://gwyddion.net/documentation/user-guide-en/file-formats.html
Could you tell me which one?
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Wang-stables
commented on June 11, 2024
Ok, they tell me that we are using Veeco ll and Veeco lll, also we usually
use the nanoscope analysis 3.00 for analysis.
Again, thank you for sending the email for discussion.
我想匿名我想匿名 ***@***.***> 於 2023年3月6日 週一 下午3:21 寫道：
… Thank you for your asking, I'm asking others if they know the true format
is, because I can't sure about this.
Olivier Scholder ***@***.***> 於 2023年3月6日 週一 上午5:44寫道：
> .spm is not a Bruker file format, so you cannot use the Bruker module to
> load it. Unfortunately many instruments are using the spm extension:
> http://gwyddion.net/documentation/user-guide-en/file-formats.html
> Could you tell me which one?
>
> —
> Reply to this email directly, view it on GitHub
> <#30 (comment)>, or
> unsubscribe
> <https://github.com/notifications/unsubscribe-auth/A3SVF5Y24OXP3E7V3PWUJSTW2UCMZANCNFSM6AAAAAATO2SWSM>
> .
> You are receiving this because you commented.Message ID:
> ***@***.***>
>
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Related Issues (20)
- Calibration of ITM files HOT 1
- https://github.com/scholi/pySPM_data. This URL could not be found . HOT 7
- D:\Anaconda\lib\site-packages\pySPM\data\CristA_0002.xml HOT 3
- Scaling parts of the spectrum HOT 3
- Wired z axis values HOT 4
- Issue with median of differences correction HOT 2
- "li" variable not defined in ITM.py HOT 6
- reuse file format reader in afmformats HOT 3
- Defining regions of interest (ROI) HOT 2
- Nonsquare scans Bruker files (.spm) HOT 5
- SurfaceLab7 .itax & .itm file support HOT 8
- lower case augment support for get_channel() struct.error: unpack requires a buffer of 369664 bytes HOT 1
- Error when opening an ITM File generated by Surface Lab 7 HOT 2
- Bruker spm format: request for explanantion of overall scale computation HOT 1
- Question: basic plotting code HOT 1
- Controlling image axix label size font type..etc HOT 1
- Error while using correct_lines/ correct_slope on .spm- (Bruker-) data with different x-,y-dimension HOT 2
- Unable to read a SXM file from Nanonis HOT 11
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