Adam Taranto
Adam Taranto
In response to your last question, yes these are all just different ways to chain the steps together. In your example: ```bash # Index the draft genome assembly samtools faidx...
Does this address issue in #1708?
@tanghaibao was there a reason that numpy version was fixed as < 2 ?
@xiaoguizz Can you please post your solution here, it may help future users. Are you trying to do the analysis using whole genome alignments?
Please provide more information. Which tool are you trying to use? Can you provide an sample image showing what is going wrong?
I see, so your problem is that the very large first contig has caused everything else to be scaled down? I think your best option is to plot the first...
Opened a PR on the conda-forge feedstock https://github.com/conda-forge/colormap-feedstock/pull/5
Lol, yes I did not read the giant text banner on the 2022 release saying that it is not actually the latest release. I don't think the is a way...
Tried to fix this in #760 but Hatchling is rejecting valid SPDX strings in the format that setuptools is migrating to. See: https://github.com/pypa/hatch/issues/1708 I don't think this should be happening...
Try downgrading to `setuptools