Closed adityabandla closed 6 years ago
Hi Aditya Bandla
There is no need for scaffolding. The package works equally well for contigs.
Thanks Rasmus! I sequenced 27x samples across 2 lanes on the HiSeq (250bp). These samples are spatially related and I see differences in the relative proportions of my target organism (whose genomes I am trying to assemble).
I did a composite assembly i.e. combined reads across all 27x samples into a single file which was then assembled. I then mapped each sample individually back to the contigs to estimate coverage. Is this considered a valid approach?
Thanks for the advise!
Hi Aditya Bandla
Yes that is often how we run it. Coassembly of all reads and then making coverage files for each of the samples by individual mapping.
Hi,
I used MEGAHIT to assemble a sediment metagenome. However, I ran into issues with finding a suitable scaffolder for converting the contigs to scaffolds.
Can I go ahead with the mmgenome workflow only with contigs? Is there a recommended scaffolder for metagenomic contigs?
Thanks