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Table 2 Conditioned Forbes scores after partitioning the exome into successively finer nucleotide contexts

From: Origins and characterization of variants shared between databases of somatic and germline human mutations

Model class

Partitions into which nucleotide context

Number of partitions

Number of expected shared variants

Partition-conditioned Forbes coef

Total shared SNVs explained

Incremental explanatory value

Statistical Independence

Unpartitioned

1

115,814

2.910

34.4%

34.4%

Basic mutation type

Deamination vs transition vs transversion

3

294,619

1.144

87.4%

53.0%

Extended nucleotide context

Trinucleotide

96

301,728

1.117

89.5%

2.1%

Pentanucleotide

1536

305,511

1.103

90.7%

1.2%

Heptanucleotide

24,576

307,393

1.096

91.2%

0.5%