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1.
Figure 3

Figure 3. From: Speeding disease gene discovery by sequence based candidate prioritization.

Receiver Operating Characteristic (ROC) curves. Receiver Operating Characteristic (ROC) curves for the training set (A) and the two test sets (B and C). The true positive rate is measured along the y-axis and the false positive along the x-axis. The area under the resulting curve is a measure of classifier performance.

Euan A Adie, et al. BMC Bioinformatics. 2005;6:55-55.
2.
Figure 2

Figure 2. From: Speeding disease gene discovery by sequence based candidate prioritization.

The alternating decision tree. The alternating decision tree used to classify instances. A gene is classified with the tree by beginning at the node marked "Start" and then following each branch in turn. Upon reaching a node which contains an assumption the "yes" or "no" branch is followed as appropriate. If the relevant feature is "unknown", neither branch is followed. Adding up each of the numbers in rectangles that are encountered along the way results in a final score which reflects the relative confidence of the classification. The classification itself is based on the sign of the score.

Euan A Adie, et al. BMC Bioinformatics. 2005;6:55-55.
3.
Figure 4

Figure 4. From: Speeding disease gene discovery by sequence based candidate prioritization.

Performance over artificial loci. Relative performance on the sets of artificial loci created from the training set (yellow line), HGMD test set (the blue line) and oligogenic test set (the green line). The gray line represents the value expected if there had been no enrichment. The x axis represents the % of the ranked list in which the target gene was found; the y axis represents how frequent that occurrence was. For example, in the training set (the yellow line) the target gene was in the top 30% of the ranked list around 56% of the time.

Euan A Adie, et al. BMC Bioinformatics. 2005;6:55-55.
4.
Figure 1

Figure 1. From: Speeding disease gene discovery by sequence based candidate prioritization.

Histograms of selected features. Histograms showing distributions of selected features in both "disease genes" (those listed in OMIM) and control genes (those not). Data was binned for graphing purposes. Distributions are shown for (A) gene length in kilobases; (B) protein length in amino acids; (C) % identity of the best reciprocal hit (BRH) homolog in mouse; (D) Ka (a measure of non-synonymous change between species) of the BRH homolog in mouse; (E) number of exons and (F) 3' UTR length in basepairs.

Euan A Adie, et al. BMC Bioinformatics. 2005;6:55-55.

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