Luke,
I record excitatory interneurons in the brainstem that are responsible for respiratory pattern generation. In slice preparations, they exhibit synchronized bursts of action potentials. Network activity can further be monitored on motor nerve rootlets contained in the slice. Over the years classification schemes have been proposed that parcel these rhythmically active neurons into categories based on the trajectory of membrane voltage during each cycle, latency of activation (with respect to the population as a whole) and also by a suite of membrane currents and pharmacological sensitivities. To arrive at a conclusion about "what kind" of rhythmic respiratory neuron you are recording from one typically has to record baseline activity for awhile and pair that with suction electrode recordings of fictive motor output. After that I would (by hand/feel) adjust the bias current up and down to look for baseline dependent non-linearities or voltage-dependent pacemaker properties. This would be followed by a more 'standard' recording where membrane currents are elicited in synaptic isolation/with pharmacology. So the first half of experiments lends itself to gap-free acquisition, while the second half is more of a traditional sweep-based stimulus-response recording.
Unfortunately there is a lot of effort needed to call a duck a duck... To that end, I want to build a data set that I can use to train a classifier (post hoc) and later apply that trained algorithm to help predict cell classifications (in the best case, online during live cell experiments) without having to spend 30+ minutes washing in drugs and iteratively assaying membrane currents. My short term goal is to hopefully apply such a classifier toward PatchSeq in order to more rapidly sample isolates of "known" phenotype. The more distant goal is to use it for more elaborate experiments involving synchronized calcium imaging and/or stimulation. BUT I need good, clean, standardized training data that simply isn't out there on any repositories right now. To get it I will be making recordings in the paradigm I described above--thus the desire to have some sort of running data display or acquisition. To get the many many replicates I will likely need it would seriously help to semi-automate my work flow, so that's why I am here. I think there is enough I can use or build off of in ACQ4 to ramp up the rate at which I acquire cells both for the training data set and later PatchSeq sampling.
To answer your other questions directly:
Yes--we would want to store to disk during continuous acquisition.
I would primarily want to roll holding current slowly up and down, which I could do manually from the amplifier. For the immediately planned experiments, no. I would not need to access other devices during that time.
Yes. Stimulus-response could interrupt continuous acquisition. At that point, we will have the network silenced via synaptic isolation.
Are you able to elaborate on your suggestion? For now I am just running my signal through a external digital oscilloscope so I can see what is going on. When I am finished getting the amplifier more tightly integrated and have my Sensapex manipulator interacting as it should, I might have a go at it.
Cheers,
Wiktor