(PRESS) Point resolved spectroscopy is a multi echo single shot technique to obtain spectral data. PRESS is a 90°-180°-180° (slice selective pulses) sequence. The 90° radio frequency pulse rotates the spins in the yx-plane, followed by the first 180° pulse (spin rotation in the xz-plane) and the second 180° pulse (spin rotation in the xy-plane), which gives the signal.
With the long echo times used in PRESS, there is a better visualization of metabolites with longer relaxation times. Many of the metabolites depicted by stimulated echo technique are not seen on point resolved spectroscopy, but PRESS is less susceptible to motion, diffusion, and quantum effects and has a better SNR than stimulated echo acquisition mode (STEAM).

A pulse sequence is a preselected set of defined RF and gradient pulses, usually repeated many times during a scan, wherein the time interval between pulses and the amplitude and shape of the gradient waveforms will control NMR signal reception and affect the characteristics of the MR images. Pulse sequences are computer programs that control all hardware aspects of the MRI measurement process.
Usual to describe pulse sequences, is to list the repetition time (TR), the echo time (TE), if using inversion recovery, the inversion time (TI) with all times given in milliseconds, and in case of a gradient echo sequence, the flip angle. For example, 3000/30/1000 would indicate an inversion recovery pulse sequence with TR of 3000 msec., TE of 30 msec., and TI of 1000 msec.
Specific pulse sequence weightings are dependent on the field strength, the manufacturer and the pathology.

See also Interpulse Times.

The schematic figures of a pulse sequence timing diagram illustrate the steps of basic hardware activity that are incorporated into a pulse sequence. Time during sequence execution is indicated along the horizontal axes. Each line belongs to a different hardware component. One line is needed for the radio frequency transmitter and also one for each gradient (G_s = slice selection gradient x, G_f = phase encoding gradient y, G_f = frequency encoding gradient z, also called readout gradient).
In picture 1, a timing diagram for a 2D pulse sequence is shown.
Slice selection and signal detection are repeated in duration, relative timing and amplitude, each time the sequence is repeated. A single phase encoding component is present each time the sequence is executed.
Additional lines are added for ADC (Analog to Digital Converter) and sampling. A gradient pulse is shown as a deviation above or below the horizontal line. Simultaneous component activities such as the RF pulse and slice selection gradient are indicated as a non-zero deviation from both lines at the same horizontal position. Simple deviations from zero show constant amplitude gradient pulse. Gradient amplitudes that change during the measurement, e.g. phase encoding are represented as hatched regions.

The second picture shows a timing diagram for a 3D pulse sequence.
Volume excitation and signal detection are repeated in duration, relative timing and amplitude, each time the sequence is repeated. Two phase encoding components are present, one in the phase encoding direction and the other in slice selection direction (irrespectively incremented in amplitude) in each time the sequence is executed. A description of the comparison of hardware activity between different pulse sequences.

Quadrature detection is used in magnetic resonance imaging as well as in Doppler ultrasound and is also called quadrature demodulation or phase quadrature technique.
With this phase sensitive demodulation technique the complex demodulated signal is separated into two components. One is called the real channel; the second part is called the imaginary channel and is located 90° away from the real channel. The signals from both channels are combined to produce a single set of quadrature detected real and imaginary spectra. In MRI, the parts of the demodulated MR signal are further processed by Fourier transformation analysis. All information on the MR signal components e.g. amplitude, phase, and frequency is given by this quadrature detection combined with Fourier analysis.

Standard compound used as a standard reference spectral line for defining chemical shifts for a given nucleus. As recommended by the ASTM, for 1H it is tetramethylsilane (TMS) and for 31P it is phosphoric acid, although for practical biological applications water and PCr have been used as secondary references for hydrogen and phosphorus spectroscopy, respectively. The reference compound can be in a capsule outside of the subject (external) or can be in the subject (internal); internal references are generally preferable where possible, as external references may be subject to different conditions.