Next, the Transcription Factor ChIP-Seq tool builds a filter, which can be used to identify genomic regions whose read coverage profile matches the characteristic peak shape and to determine the statistical significance of this match. In order to build such a filter, examples of positive (e.g. ChIP-seq peaks) and negative (e.g. background noise, PCR artifacts) profiles are needed as input. The Transcription Factor ChIP-Seq tool uses regions with very high coverage in the experiment ChIP-seq as positive examples. If control ChIP-seq experiments are given, regions with high coverage in the control and low in the experimental ChIP-seq data are used as negative examples, as they are probably originated from PCR artifacts. If there is no information to build a negative profile from, the profile is estimated from the sequencing noise.
Once the positive and negative regions have been identified, the Transcription Factor ChIP-Seq tool learns a filter that matches the average peak shape, which we term peak shape filter. The filter implemented is called Hotelling Observer and was chosen because it is the matched filter that maximizes the AUCROC (Area Under the Curve of the Receiver Operator Characteristic), one of the most widely used measures for algorithmic performance.
where is the average profile of the positive regions, is the average profile of the negative regions, while and denote the covariance matrices between the positive and negative profiles, respectively. The Hotelling Observer has already previously been successfully used for calling ChIP-seq peaks [Kumar et al., 2013]. An example of Hotelling observer is shown in figure 33.4.