Linker DNA Length

Derive linker DNA length from repeat and core-particle lengths.

Description

Linker length is the difference between nucleosome-repeat and core lengths.

Linker length is the difference between nucleosome-repeat and core lengths.1

Derive linker DNA length from repeat and core-particle lengths.

When to use Linker DNA Length

Use this tool to derive linker DNA length from repeat and core-particle lengths.

Prepare the already measured signals, counts, coordinates, fitted coefficients or sequence strings requested. Keep assay definitions, units, aligned lists and caller-selected thresholds consistent.

How to use Linker DNA Length and understand its results

  1. Prepare the already measured signals, counts, coordinates, fitted coefficients or sequence strings requested. Keep assay definitions, units, aligned lists and caller-selected thresholds consistent.
  2. Enter nucleosomeRepeatLengthBp, coreParticleLengthBp using the field table and calculation rules, then run the tool.
  3. Read linkerDnaLengthBp, positiveLinker. The explanation below defines the units, signs, ordering and any flags or placeholder values.
  4. If the tool reports an input issue, correct the values and run it again. Apply the stated assumptions when interpreting a successfully returned result.
Input fieldMeaningValue type; see rules belowRequirement
nucleosomeRepeatLengthBpNucleosome repeat length (bp)number; minimum: 0Required
coreParticleLengthBpCore particle length (bp)number; minimum: 0Required

Enter nonnegative lengths; return signed difference and strictly positive flag.

linker=repeat−core

Units, indexing, boundary conditions and exceptional cases are defined in the calculation rules above.

Output fieldMeaningValue type
linkerDnaLengthBpLinker DNA length (bp)number
positiveLinkerLinker length is positiveboolean
json
{
  "input": {
    "nucleosomeRepeatLengthBp": 200,
    "coreParticleLengthBp": 147
  },
  "output": {
    "linkerDnaLengthBp": 53,
    "positiveLinker": true
  }
}

Limitations and assumptions

Negative results are preserved. No structure or spacing is measured.

Numeric inputs, where present, must be finite. Follow the calculation-specific rules for overflow, underflow and exceptional cases. Missing required fields, extra fields, wrong value types and violations of the calculation rules are input errors. A successfully returned false flag is an evaluated outcome; its meaning is explained above.

Alternative or Complementary methods

Use Nucleosome Repeat Length: Estimate nucleosome repeat length from ordered periodicity peaks. For a complementary task, use Nucleosome Positioning: Classify nucleosome positioning from center dispersion.

References

  1. Linker DNA Length — tool.io

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