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Hi,
what about the idea to add an viewer for sanger sequencing results?
maybe one of these could be implemented ?
https://github.com/y9c/cfutils
https://github.com/labsquare/CutePeaks
https://…
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This entry was created as part of issue #866 by @erasche on 2016-02-11. I split the issue to address separately.
#
- [ ] Zoom level is too restrictive:
- [ ] My users want to zoom further, it's ha…
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Hello, is it possible to run EditR via command line via e.g., passing the gRNA sequence and the .ab1 as input?
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Very similar concept to images task, except we create Sequence rows.
* Sequences are copied or dropped in
* If dropped in the back end reads the fasta file, creates the sequence, and returns the se…
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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/rodrigarc/scifer
Confirm the following by editing…
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Hey guys,
I formatted both the BAR and NO_BAR databases compiled and provided by you for use with dada2's taxonomy assignment function. dada2 uses the RDP classifier for sequence classification.
…
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Hi,
I'm indirectly using io_lib via biobambam2 so this is primarily an attempt to isolate where the problem may lie. My understanding is that CRAM conversion is handled by `io_lib`.
I'm finding…
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Using `Tools > Sanger Data Analysis > Read quality control and alignement`, in the `FASTQ Quality Trimmer` box if I set the quality greater than 0, all the sequences are discarded.
I think the FAST…
hadim updated
7 years ago
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```
What steps will reproduce the problem?
I have forward and reverse reads but the finished sequence is not being
created. The sequences are aligning fine but there is no "finished sequence". I
as…
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```
What steps will reproduce the problem?
I have forward and reverse reads but the finished sequence is not being
created. The sequences are aligning fine but there is no "finished sequence". I
as…