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[[File:Nanopore_sequencing_principle.png|thumb|right|320px|Nanopore sequencing principle. Openly licensed schematic used as a general visual guide.]]
[[File:Nanopore DNA sequencing.png|thumb|right|320px|DNA movement through a nanopore can be converted into a measurable signal. Source: Wikimedia Commons, CC BY 4.0.]]
[[File:Detection pics scipy signal find peaks.svg|thumb|right|320px|Peak or event detection concepts support nanopore signal analysis. Source: Wikimedia Commons, CC BY-SA 4.0.]]
'''Fundamentals''' is part of the Nanopore Wiki learning path. Nanopore signals arise from ionic transport, pore geometry, molecular occupancy, electrostatic interactions, and measurement noise.
'''Fundamentals''' is part of the Nanopore Wiki learning path. Nanopore signals arise from ionic transport, pore geometry, molecular occupancy, electrostatic interactions, and measurement noise.



Revision as of 10:56, 30 June 2026

DNA movement through a nanopore can be converted into a measurable signal. Source: Wikimedia Commons, CC BY 4.0.
File:Detection pics scipy signal find peaks.svg
Peak or event detection concepts support nanopore signal analysis. Source: Wikimedia Commons, CC BY-SA 4.0.

Fundamentals is part of the Nanopore Wiki learning path. Nanopore signals arise from ionic transport, pore geometry, molecular occupancy, electrostatic interactions, and measurement noise.

Core concepts

  • Conductance links current, voltage, pore geometry, and solution conductivity.
  • Access resistance becomes important at nanometer length scales.
  • Electrophoresis and electroosmotic flow can both affect capture and translocation.
  • Filtering can reduce noise but also distort fast events.

Concept map

Step Description
1 Voltage drives ions and charged molecules through or near the pore.
2 The pore and nearby access regions set the baseline conductance.
3 A molecule changes the local conductive pathway and produces an event.
4 Electronics and signal processing determine what features remain observable.

Typical applications

  • Interpreting current traces.
  • Choosing voltage, salt concentration, sampling rate, and bandwidth.
  • Understanding why experiments fail or produce ambiguous signals.

Common pitfalls

  • Raising voltage without considering pore stability and molecule damage.
  • Over-filtering data until events look cleaner but lose true kinetics.
  • Comparing event amplitudes without normalizing for open-pore current.

References