File commands
fo open UCSF NMR data, a Felix matrix, or a Sparky spectrum file
fs save a Sparky spectrum annotation file
fa save spectrum with a new name
jo open several spectra at once
js save all spectra
ja save project with a new name
View commands
ci change background color
xh display view scale axes in Hz
xp display view scale axes in parts per million
vc center a view on the selected peak
vs show scales (ppm, hz, or index units) along view axes
vp show peak position / height / linewidth in status bar
vR show resonances along edge of spectrum
vd make another view window
zf show entire spectrum
zi zoom in by a factor of 2
zo zoom out by a factor of 2
Peak commands
at make assignments
dr delete resonances not used in any peak assignments
pc center selected peaks at local maxima or minima.
pg create a peak group from selected peaks
lu move labels so they don't overlap each other
pa select all peaks in a spectrum
Dialogs
tb table of chemical shifts
ct set contour levels and colors
ot change ornament colors and sizes
lt show a list of peaks for a spectrum
rr rename atoms and groups
rl list group/atom chemical shifts, standard deviations
yt make views scroll in parallel
Pointer Modes
F1 click or drag to select or move peaks, labels, lines, ...
F2 clicking centers view on point
F3 place vertical and horizontal grid lines
F4 add a line extending across whole spectrum
F5 add a line extending across whole spectrum
F6 add a text label to a peak
F7 add a horizontal or vertical line between end points
F8 click to place a peak or drag to find peaks
F10 click or drag to integrate peaks
F11 drag to select a new region to show
F12 drag to zoom and duplicate a view
Pressing the shift key and clicking on a selected peak will deselect it without deselecting
other selected peaks.