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As team lead Sequencing Operations (James M) we would like to add the “name” field from the “Programs” table in the Sequencescape database to the MLWH. This will enable us to identify studies by Sange…
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Hello,
Thanks for this amazing tool.
Any recommendation on the best approach to take when one has multiple paired-end fastq files for the same sample? An example is the 1000 genome 30X WGS file…
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As a user I would like to see the IRods root collection path for my samples so that I can find my sequencing data.
**Acceptance Criteria**
- [x] Add a new column to the Sample Tracking view in the d…
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**Is your feature request related to a problem? Please describe.**
Many clinical relevant regions are difficult to sequence via NGS due to low complexity and homology (see #529). Usually, these diagn…
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**Describe the Housekeeping**
As an SSR, I would like the HiSeq-related submission templates to be removed from the dropdown list when creating a submission, because the HiSeq instruments are no long…
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As TL I would like to understand why the cost code and platform columns are showing null for most plates.
**Acceptance Criteria**
- [ ] Compare rows that have valid cost code and platform results ag…
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see this thread on the mailing list
http://lists.open-bio.org/pipermail/biojava-l/2016-July/011489.html
A test file is here
https://github.com/biopython/biopython/blob/master/Tests/Abi/3730.ab1
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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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Hi all,
I am trying to install metAMOS on CentOS 6.5, after installing all the program and dependencies guide suggesting to check if the program is installed well. To do that, i was asked to run run_…