Bench modeSteps, parts, and safety only. Big type for a phone at the bench.
Phase 6

Beyond the scalp

The invasive, neuromodulation, materials, and wet-lab frontier. Most of it happens inside a lab.

Scalp EEG is one small corner of the field. The largest market is neuromodulation, the most dramatic results are intracortical, and the hardest unsolved problems are materials and packaging. This phase is a guide to that territory, with projects that mostly require a lab and a mentor.

Everything before this phase could be done in a dorm room. This phase cannot, and it should not be. Stimulating tissue, fabricating microelectrodes, and recording from animals belong in a lab with a mentor, an IRB or IACUC protocol, and a safety officer. The projects here are written for the student who has climbed the research ladder from Phase 1 and is now trusted with real equipment.

If you are not there yet, read the explainers anyway. Understanding neuromodulation mechanisms, stimulation safety, the foreign body response, and the industry landscape is what makes you useful in an interview at any of the companies thirty minutes from campus.

There is no “ready when” that ends this phase, because this is where the field itself currently ends.

Projects

Choose one. Do a second if hooked.

Explainers

Theory that attaches to what you just built. Read after doing.
Explainer

Neuromodulation, mechanisms and evidence

Deep brain stimulation, spinal cord stimulation, vagus nerve stimulation, cochlear and retinal implants, focused ultrasound, TMS, and tDCS. What each does to tissue, what the evidence says, and the honest state of "we do not fully know why it works."

16 min
Explainer

Stimulation safety and electrochemistry

Charge density, the water window, the Shannon limit, charge balance, and why stimulation electrodes corrode. The chemistry at the interface when you push current the other way.

12 min
Explainer

Electrode materials and the foreign body response

What the brain does to a thing pushed into it, why recordings degrade over years, and the materials strategies (softer, smaller, coated, dissolving) being tried against it. The central engineering problem of chronic implants.

12 min
Explainer

Packaging, power, and telemetry

Sealing electronics against body fluid for decades, getting a hundred channels through the seal, powering an implant without wires, and sending the data out. The unglamorous problems that decide whether a brain implant is a product.

12 min
Explainer

The Utah Array, a history

From a Utah bioengineering lab in the late 1980s to the electrode in nearly every human intracortical BCI study, with the company, the regulatory path, and the limits that the next generation is trying to pass. Local history that happens to be the field's history.

10 min
Explainer

The industry landscape

Who is building what, from implanted BCIs to neuromodulation giants to consumer headbands to research hardware, what each hires for, and how to read the field's news without being fooled. Dated, and meant to be re-checked.

12 min

Ready for Phase 7 when

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What an interviewer would ask

If you can answer these, you are done here
  1. Why does a recording from a Utah Array degrade over years, and what are the leading approaches to fixing it?
  2. What is the Shannon limit and what does it not tell you?
  3. Compare DBS, spinal cord stimulation, and vagus nerve stimulation: mechanism, indication, and market.
  4. How would you design a hermetic feedthrough for a hundred channels? What has stopped people?