Tilt series data were acquired at various mags, resulting in either 5.8 or 8.9 Å pixel dimensions. Image width and height are variable.
# Budding yeast chromatin is dispersed in a crowded nucleoplasm in vivo # Chen Chen, Hong Hwa Lim, Jian Shi, Sachiko Tamura, Kazuhiro Maeshima, Uttam Surana, Lu Gan # # IMOD reconstruction of yeast and chromatin cryotomograms # # Revised 20160417; IMOD version 4.8.47 3/17/2016 # This dir contains the minimal number of files needed to reconstruct the tomograms in Chen et. al. # Note that some of the tomograms need to be binned x2 to facilitate visualization. 1) Make a .st file from the .mrc tilt series and place in the correct dir (see details below). 2) Run etomo from that directory: etomo 14oct01a__014.edf 3) In etomo, execute only the following commands. Final Aligned Stack: (Create Tab) Create Full Aligned Stack (Correct CTF Tab) Select the right Falcon noise file, Correct CTF, Use CTF Correction (2D Filter Tab) Filter, Used Filtered Stack, Done Tomogram Generation: Generate Tomogram, Done Post-processing : Trim Volume, Done Clean Up : optional cleanup, Done
Create .st files as follows:
# The following use the Falcon2_20141217 noise files for CTF correction newstack -secs 1-61 14oct01a__014.mrc 14oct01a__014.st newstack -secs 0-47 14oct01a__021.mrc 14oct01a__021.st newstack 14oct01a__027.mrc 14oct01a__027.st newstack 14oct01a__032.mrc 14oct01a__032.st newstack -secs 2-59 14oct01a__052.mrc 14oct01a__052.st newstack -secs 0-60 14oct01a__067.mrc 14oct01a__067.st
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Archives and downloads the selected files into an uncompressed zip file.
Depending on the number and size of files to be downloaded, this can take an enormous amount of time.
Also, this feature is unstable and may not work properly, and checksums of downloaded files are not verified.
We recommend using rsync, aspera, globus, etc.
Download a list of selected files.
It is possible to download files by specifying the file list with rsync command, etc.