Portcullis

From the documentation:

Portcullis stands for PORTable CULLing of Invalid Splice junctions from pre-aligned RNA-seq data. It is known that RNAseq mapping tools generate many invalid junction predictions, particularly in deep datasets with high coverage over splice sites. In order to address this, instead for creating a new RNAseq mapper, with a focus on SJ accuracy we created a tool that takes in a BAM file generated by an RNAseq mapper of the user’s own choice (e.g. Tophat2, Gsnap, STAR2 or HISAT2) as input (i.e. it’s portable). It then, analyses and quantifies all splice junctions in the file before, filtering (culling) those which are unlikely to be genuine. Portcullis output’s junctions in a variety of formats making it suitable for downstream analysis (such as differential splicing analysis and gene modelling) without additional work.

See the Portcullis documentation or the GitHub repository for details.

References

• Portcullis was presented at the Genome Science 2016 conference by Daniel Mapleson: poster, slides.