Quantifying optimal accuracy of local primary sequence bioinformatics methods

摘要

Motivation: Traditional bioinformatics methods scan primary sequences for local patterns. It is important to assess how accurate local primary sequence methods can be. Results: We study the problem of donor pre-mRNA splice site recognition, where thesequence overlaps between real and decoy datasets can be quantified, exposing the intrinsic limitations of the performance of local primary sequence methods. We assess the accuracy of primary sequence methods generally by studying how they scale with dataset size and demonstrate that our new primary sequence ranking methods have superior performance.