Gene Stats Detail


Summary

  count total len % cov % gc min len max len median len mean len
Contig 14 18874889 100.00 48.23 756744 2291499 1399098.00 1348206.36
Gene 6967 13588697 71.83 49.27 102 15614 1685.00 1950.44
Exon 42284 11165780 58.99 50.56 3 4857 157.00 264.07
Coding 6967 10723623 56.81 50.89 102 14676 1284.00 1539.20
Intergenic 6853 5317494 28.17 45.57 1 58070 454.00 775.94
5' UTR 1676 128651 0.68 46.55 1 844 47.00 76.76
3' UTR 2371 313506 1.64 40.88 1 1221 97.00 132.23

Specificity/Sensitivity Analysis

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Terminology is from Burset M and Guigo R, "Evaluation of gene structure prediction programs." Genomics, 1996 Jun 15;34(3):353-67.
TP (true positives): nucleotides predicted as exonic in predictions and EST evidence; splice junctions with exact agreement, in position and type (donor:donor, acceptor:acceptor), between predictions and EST evidence; exons with both splice sites in exact agreement with EST evidence.
TN (true negatives): nucleotides predicted as intronic in predictions and EST evidence; not defined for splice sites or exons.
FP (false positives/overpredictions): nucleotides predicted as exonic where EST evidence indicates an intron; predicted splice junctions where the EST alignments do not have a splice*; predicted exons which fall entirely within an intron supported by EST evidence ("wrong" in Guigo's terminology).
FN (false negatives/underpredictions): nucleotides predicted as intronic where EST evidence indicates an exon; EST alignment splice junctions where the predictions do not have a splice*; EST-based exons that fall entirely within a predicted intron ("miss" in Guigo's terminology).
unknown (cannot be scored): nucleotides that do not touch an EST alignment; splices that do not touch an EST alignment, and initial/terminal splices that fall within an initial/terminal exon of a partial EST alignment; exons that either do not touch an EST alignment or fully encapsulate a single-exon partial EST alignment.
sn (sensitivity): TP/(TP+FN)
sp (specificity): TP/(TP+FP)
cov (coverage): percentage of predicted elements that are not "unknown"

In the very rare cases where the query predicts a donor site exactly where EST evidence indicates an acceptor (or vice versa), we count it as both FP and FN. Certain classes of incorrect exon predictions are not labeled TP, FP nor FN.

Compared 6967 predictions to 0 reference models.

  cov sn sp TP TN FP FN unknown
nucleotide - - - 0 0 0 0 13588697
splices - - - 0 - 0 0 84568
exons - - - 0 - 0 0 42284