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![340779688-b187c7d9-3607-4565-a803-6e97d72cd49b](https://github.com/user-attachments/assets/ea695806-60fd-48fc-87ec-ccaaf8243b1f)
![image](https://github.com/Bforartists/Bforartists/assets/3535740…
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In the design, the applied loads were 5.4 MN, 0.09 MN, and −8.9 MN in the x, y, and z directions, respectively. The moments were −1.6 MN m, −13.3 MN m, and 10.8 MN m in the x, y, and z directions, res…
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### Please make sure these conditions are met
- [X] I have checked that this issue has not already been reported.
- [X] I have confirmed this bug exists on the latest version of scanpy.
- [x] (option…
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We will track these properly somewhere, (and document ) as I guess it could happen a lot ....
Original SPNCRNA the last one used was SPNCRNA.1712 nc-pho1
SPNCRNA.1713 reserved for Mo
Jurgs blo…
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The spec does not expressly forbid conflicting Units of Information containing controlled vocabularies of the same type. For example it is possible to define a macromolecule with both a protein (mt:pr…
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I really like your preprint and I would love to use it for direct RNA sequencing.
Do you happen to work on adjusting the UNCALLED for direct RNA sequencing? Given that an accurate RNA k-mer model is …
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Dear CNVkit developers,
I am trying to get import-rna to work but I am getting an error. My command was
`cnvkit.py import-rna --format rsem expression/*/*.genes.results --output cnvkit_summary.…
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I tried to predict two RNA strands with cas9 (PDB ID: 4OO8).
However, RNA structures were crashed like fragment of skein.
Not only for this, but also same RNA structure were simulated without protei…
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Does TElocal work with long read bulk RNA-seq? If so, has anyone done this, and, are there any reccomrecommendations on how to run it?
Thank you,
FR
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I am interested in calling all the mismatches/conversions in my RNA modification dataset that is generated using Illumina TruSeq protocol (dUTP). I am using the JACUSA2 pileup method for this step. Si…