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Table 1 Overall statistics of the RNAz screen. Initial filtering of Pecan alignments leaves roughly 50% as input for RNAz respectively to the ncRNA prediction. The distribution of RNAz hits does not show a chromosomal bias. We counted the number of predicted loci and their overall length at two probability thresholds (p > 0.5, p > 0.9) for normal and also randomized alignments. Obtained relative frequencies (given as percentages) can be interpreted as false discovery rates (FDR). As expected, the FDR decreases with a higher RNAz p-value.

From: Computational RNomics of Drosophilids

 

overall

chromosomes

  

2L

2R

3L

3R

4

X

alignments

4077

659

804

676

861

65

1012

aligned DNA [Mb]

117

22

21

23

28

1

22

screened by RNAz [Mb]

57.4

11

10

12

14

0.4

10

percentage

49

50

48

52

50

40

46

RNAz p > 0.5

42 482

7 824

6 646

8 765

10 351

196

8 700

   [Kb]

5 079

927

783

1 060

1 229

25

1 055

RNAz p > 0.9

16 377

2 940

2 473

3 413

3 862

80

3 609

   [Kb]

2 167

385

321

461

511

11

478

FDR p > 0.5 hits

56.5

54.5

57.2

57.5

55.9

68.4

57.3

   sequence

52.8

50.7

53.6

53.9

52.4

64.0

53.0

FDR p > 0.9

45.3

43.6

45.1

47.8

46.2

43.7

43.8

   sequence

40.2

38.2

40.2

42.5

41.1

36.4

38.7