Skip to main content
. 2015 Sep 8;11(9):e1005508. doi: 10.1371/journal.pgen.1005508

Table 1. Whole genome sequencing of mutant strains used in this study.

Strains Index Total reads Aligned reads Cover-age % Aligned # Total Changes # Unique changes # Putative changes* # Changes within mapping intervals Gene
pf7 TGAGGTT 113958070 106694994 90 94 67691 1505 4 1 CCDC40
pf8 GCTTAGA 104812850 97145742 82 93 73576 1423 4 2 CCDC39
fla12 TGAGGTT 51316544 31759955 27 62 51987 27145 43 2 CCDC39
pf7; pf8, cnk11-1 AATTCAT 49851384 37785929 32 76 104759 41459 9 n/a CNK11
pf7; pf8; cnk11-2 TTTGGCG 50434300 39846537 34 79 74763 25267 8 n/a CNK11
pf7; pf8; cnk11-3 AGGCGAA 52468650 47265275 40 90 81264 10272 59 n/a CNK11
pf7; pf8; cnk11-4 CCGATTA 63095732 60194808 51 95 49140 1505 18 n/a CNK11
pf7; pf8; cnk11-5 TAACAAG 49771244 38235224 32 77 90782 35558 11 n/a CNK11

* Changes are defined as being within coding regions or at intron-exon boundaries and have a Phred quality score ≥100.