Closed ammaraziz closed 8 months ago
Hurts my head, but that is what you do, isn't it? HAHAHAHAHA
- [ ] Use scrubby for human removal step
I can't seem to get scrubby installed via Conda. I have raised an issue on scrubby's GitHub page. Until the issue is resolved, I can do it manually by performing only kraken2 host reads extraction.
See my comment on the github page about how to install scrubby
.
get uniquely mapped reads for ct_ref.fasta alignment
Can you please create a unique set of references for this?
It's okay if you want to test independent tools but we should aim to update the pipeline as we go along.
See my comment on the github page about how to install
scrubby
.get uniquely mapped reads for ct_ref.fasta alignment
Can you please create a unique set of references for this? Ct_refs.zip
I have got four representative genotypes here. I have some more work to do here on getting the best references to use for each body site but that will wait as it is part of another project that I am doing. Yes, the other project is comparing all Ct reference genomes and creating the best consensus sequence for each strain. For this I am using Illumina, nanopore to sequence all reference strains and then some historical 454 gap-closed genomes that the lab currently has.
For now, I think we can proceed with the four reference strains that I have included in the attached file as they are quite unique genotypes... quite different from each other (see below).
- [ ] replace spades with shovill I think, according to the documentation, shovill only works well on isolates. Most of the samples I envisaged this pipeline will be used for will be clinical samples which will most likely be metagenomes thus making shovill not very fit for purpose??
Most of these have been completed or we've changed course.
samtools coverage
, compute meanmapq for each genome hit.ct_ref.fasta
alignment