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**Briefly describe what you hope to achieve:**
I am trying to load a series of .fcs files located in a network folder that may or may not contain only .fcs files. The plan would be to use cyto_save …
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Thank you for your wonderful packages.
I use flow cytometry in the non-classical way, to analyse ratiometric experimental quantities, rather than count the proportion of of different populations wi…
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Update the following URL to point to the GitHub repository of
the package you wish to submit to _Bioconductor_
- Repository: https://github.com/ebecht/infinityFlow
Confirm the following by edit…
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Dear Sergey,
I just finished a canu 2.0 assembly of a diploid 2.3 gbp pacbio plant genome, which turned out to be quite fragmented and much shorter than expected. There are some issues with genome …
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**Describe the bug**
I have a dataset of about 1900 FCS files from the BD Accuri C6, which used to load just fine into a flowSet when running R 3.6.3.
After updating to R 4.0.2 I get a fatal R err…
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**Describe the bug**
The ranges written on disk are integers, truncated to the lowest values, but data are not truncatedwhen read back. I don't understand at all. If I am wrong (because tired), let m…
SamGG updated
3 years ago
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Hi Sergey,
I tried to assemble an allotetraploid genome which has 900M as haploid genome size. I ran HiCanu with the below options and the output data.contigs.fasta has 2.4G size. Although I expecte…
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Hi @KamilSJaron, @tbenavi1!
I used both Smudgeplot and Genomescope2 for the early stages of my assembly project last year and you have been really helpful(issues #36 and #45 for some context) for m…
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@gfinak and @mikejiang , cytoqc is amazing and can't wait for its Bioconductor launch, thank-you!
I was able to fix channel names, however, got stuck with marker names:
```
res res
# A tibble: 2 …
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Update the following URL to point to the GitHub repository of
the package you wish to submit to _Bioconductor_
- Repository: https://github.com/JhuangLab/CytoTree
Confirm the following by editi…
ytdai updated
4 years ago