Abstract. While the discovery of structural variants in the human population is ongoing, most methods for this task assume that the genome is sequenced to high coverage (e.g. 40x),...
Background: Using microarray and sequencing platforms, a large number of copy number variations (CNVs) have been identified in humans. In practice, because our human genome is a d...
The comprehensive annotation of non-coding RNAs in newly sequenced genomes is still a largely unsolved problem because many functional RNAs exhibit not only poorly conserved sequen...
An important area of data mining is anomaly detection, particularly for fraud. However, little work has been done in terms of detecting anomalies in data that is represented as a g...
Abstract. Repairing a database means bringing the database in accordance with a given set of integrity constraints by applying modifications that are as small as possible. In the ...