LOD Score Calculator

Calculate LOD score (logarithm of odds) for linkage analysis between a genetic marker and a disease locus. LOD > 3 is strong evidence for linkage.

🧬 Genetics📐 Z(θ) = log10[L(θ) / L(0.5)]🧬 Biology
Number of recombinant offspring
Number of non-recombinant offspring
Please enter valid values.

Formula & Reference

VariableSymbolFormulaUnits
LOD Score Calculator—Z(θ) = log10[L(θ) / L(0.5)]dimensionless

Step-by-Step Examples

Example 1
Strong Linkage Signal

8 recombinants out of 50 offspring (theta ~ 0.16).

  • L(0.16) = 0.16^8 x 0.84^42
  • L(0.5) = 0.5^50
  • Z(0.16) = log10[0.16^8 x 0.84^42 / 0.5^50]
  • Calculates to Z > 3: strong evidence for linkage
✓ Z > 3 at theta ~ 0.15 (strong linkage)
Example 2
Weak Signal

4 recombinants out of 20.

  • theta_estimate = 4/20 = 0.20
  • Small sample: LOD may not reach 3
  • Need more families for reliable linkage detection
✓ Small sample: LOD < 3 likely (insufficient power)
Example 3
Exclusion

Many recombinants: 48 out of 100.

  • theta = 0.48, near 0.5
  • Z(all theta) will be negative
  • LOD < -2: exclude linkage in this region
✓ LOD < -2: evidence AGAINST linkage at this locus

Real-World Applications

Common Mistakes to Avoid

⚠️
LOD > 3 is conventional threshold

LOD = 3 means 1000:1 odds in favor of linkage. This threshold accounts for the multiple testing problem of testing all chromosomal locations.

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LOD < -2 excludes linkage

LOD < -2 is conventional threshold to exclude linkage. Means less than 1:100 odds favoring linkage at that theta.

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Sum LOD scores across families

One advantage of LOD scores: sum across independent families. Combined LOD > 3 even if individual families are uninformative.

Frequently Asked Questions

What is LOD score? ▾
LOD = log10 (Likelihood of linkage at recombination fraction theta / Likelihood of no linkage). LOD = log10[odds ratio]. LOD > 3 is accepted as significant evidence for linkage.
What is the significance threshold LOD = 3? ▾
LOD = 3 corresponds to 1000:1 odds in favor of linkage. Chosen to control false positive rate across all possible map positions tested (roughly equivalent to p < 0.001 corrected for multiple testing).
What is parametric vs non-parametric linkage? ▾
Parametric LOD: requires known inheritance model (dominant, recessive). Non-parametric (NPL, allele sharing): does not require genetic model. Used when mode of inheritance is unknown.
How has linkage analysis been replaced? ▾
For common variants: GWAS using millions of SNPs. For rare disease genes: exome/genome sequencing within families. LOD score linkage analysis still useful for rare diseases in large families.
What is multipoint linkage? ▾
Uses multiple markers simultaneously (rather than one marker at a time) to increase power. Implemented in LINKAGE, MENDEL, and other software packages.

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