I know that you're working on version 2.0 of analysis, but thought I would
mention some thoughts on the display cells function, and also what I believe
is an error using it:
1) The error: When displaying Leucine spin systems, it seems that analysis
cannot differ between the carbon values of Cda and Cdb when building the
cells. I have spin systems where the two carbon shifts are assigned to
different ppm values, but analysis always makes two Cd-lanes with the same
ppm-value. Furthermore, it usually displays the Cg lane before the Cb lane.
It should be displayed by ascending carbon-shift values.
2) Secondly, optimizing the display cells can be achieved by removing the
amide cell line, and also the cell lines displaying He2a and He2b in Asn and
Gln from the window. Apart from speeding up the display process, the
optimization leaves more room on the screen for better overview and easier
assignment of peaks.
I must mention that I use display cells for assignment of HCCH-TOCSY, and
haven't considered if the lanes I see as not necessary are important in
other types of NMR experiments.
Kind regards
Robert, Uni. of Copenhagen
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