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. 2013 Nov 7;196(1):313–320. doi: 10.1534/genetics.113.158758

Table 1. Ten candidate mutations called by GATK (i.e., sites having a read pattern consistent with a genuine single nucleotide or indel mutation) and one confirmed deletion mutation (X 2,693,102) called only by Pindel.

Read depth Read depth in mutant individual
Location Detected by GATK (G) or Pindel (P) Mutation event Offspring code Female parent Male parent Offspring mean Wild-type base Mutant base Confirmed
2L 2,301,848 G A→C 90 28 39 50.4 30 11 Yes
2L 5,955,655 G C→T 88 42 47 33.0 15 16 Yes
2L 19,399,106 G G→T, A (two individuals) 74, 88 23 36 13.8 10, 4 11, 8 Yes
2R 6,136,602 G G→A 89 33 35 61.3 21 24 Yes
2R 14,887,552 G C→A 84 39 32 64.5 45 9 No
2R 16,372,704 G C→T 89 26 27 49.4 32 17 Yes
3L 10,514,561 G, P Deletion TAAAAATGCTCT 94 32 17 52.2 16 14 Yes
3R 1,431,265 G C→T 89 32 34 44.8 33 6 Yes
3R 7,755,276 G G→A 79 26 56 55.3 50 20 No
3R 1,2126,610 G, P Deletion TCTCCGAAATAGG 84 28 34 48.7 22 15 Yes
X 2,693,102 P Deletion TGTT 94 34 21 59.3 39 12 Yes

GATK, Genome Analysis Toolkit.

HHS Vulnerability Disclosure