Brief note that we just released rastair v2.0.0 - this is a major version upgrade and not 100% command-line identical to rastair 0.8 which is used in methylseq. However, the differences are very minor so it should be fairly easy to adapt. The key difference between v0.8 and 2.0 is
much more powerful variant calling. Rastair2 now features a full-fledged variant caller under the hood, which will not only identify SNPs that affect CpGs and adjust the estimated beta accordingly, but also identify SNPs that
create a CpG and call methylation there. This adds several hundred thousand additional methylated positions in an average human genome! You can also get full-fledged vcf output in addition to the per-position and per-read bed formats as before.
We have tested Rastair2 against both TAPS+ as well as Illumina's 5-Base data, and I'm happy to say that it works extremely well on both: our SNP calling accuracy is as good or better than Illumina's DRAGEN pipeline on 5-base data, and nearly as good as GATK's haplotypecaller on WGS data, while being orders of magnitude faster. For some preliminary results, see
https://www.rastair.com - a more comprehensive pre-print is in the works.
It would be great to get some feedback from the community and hopefully upgrade nf-core to include that new version. I'm not (yet) very familiar with how nf-core pipelines are put together, but I'd happily consult on what needs changing to migrate from 0.8 to 1.0. If you just want to test stuff out for now, the docker build of v2.0.0 is available, and we're also nearly there with a bioconda recipe. There's also binaries for Linux & Mac, see the website above for details.