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Add modal for adding Orphanet ID to an Interpretation once "Associate Disease" button hit.
Add "Edit Associated Disease" button to interpretation if disease has already been associated (let me know i…
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Hi @benjjneb ,
I'm repeatedly seeing a wide distribution of sequence lengths after merging when running dada2 on my data. I thought this could be due to the variance of sequnce quality by sample, so …
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While processing the report-ready.Rmd file noticed two problems.
Script include R 'reshape' library, but installed is 'reshape2'.
After manual install of 'reshape', script stop execution at lines 85-8…
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Hello,
If there is a scaffold that has a conserved gene, meaning it is genetically similar between all organisms of a given taxa, how does it get sorted? Does it go with one bin only, such that it is…
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Hi All,
Collecting some information and opinions around RNA-seq variant calling here. The Broad institute have released best practices for germline variant calling in RNA-seq, http://gatkforums.broadi…
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Hi Pierre,
The option -c to specify the name of the sequence to be used as reference to biostar94573 is working ok. However, I still have a issue. For my reference sequence I don't have insertions an…
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It is a crosslinking method that uses UV light to cross-link RNA to Proteins without the incorporation of photoactivatable groups into RNA, followed by sequencing of the linked RNA.
References
Sander …
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Hi there,
I am currently having a problem with interpreting the results from dNdSRateAnalysis.bf. When I tried to export the results (Analyses -> Results -> Save results), I faced with 2 likelihood-f…
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General question--how should topology proposals be organized, and how should they be matched with `System` construction?
Currently, under the small molecule scheme, there is:
- `Transformation`
- `…