I am going through the Roadmap Epigenome alignment protocols, and they claim they have mapped "a total of 150.21 billion sequencing reads onto hg19 assembly of the human genome using Pash 3.0 read mapper" .
Does anyone see the reasoning for using Pash 3.0 -- which is quite an odd choice given availability of more widely adopted aligners such as Bowtie or BWA? The latter two also support multithreading, something their aligner of choice lacks.
I don't know with any certainty (thus this is a comment), but I'd guess that Pash being able to handle normal and bisulfite treated read alignment played a role. Then at least there's just one single tool that can used for everything. I wouldn't have chosen that, but that's at least an argument in favor of Pash.