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I am trying to model a protein homodimer complexed with dsDNA. I have entered in the two identical protein monomer chains as separate files and DNA strands as two separate files. In a command similar …
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http://www.html5rocks.com/en/tutorials/developertools/sourcemaps/
Now, the only way seems to be to generate the rna file and debug that file.
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Running the msi module returns the following:
`hwanho@linux:/mnt/bigHDD/resource/ref_and_tools/tools/msisensor-pro$ ./binary/msisensor-pro msi -d ./Homo_sapiens.GRCh38.dna.primary_assembly.msi.list…
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Hello MerenLab,
While at EBAME I was encouraged to open this discussion by @FlorianTrigodet and @ivagljiva, and bring it to @semiller10's attention.
DNA methylation is on the verge of constituti…
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Hi,
Could you provide the code on how to convert the original GEO data to 2 DNA sequencing + 2 RNA sequencing files to directly apply your scripts here ? Thanks.
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I was able to finish running the example prediction (rf2na.sh, ../run_RF2NA.sh rna_pred rna_binding_protein.fa R:RNA.fa) with no error messages after compilation. However, I did notice that there is n…
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Hello,
I have a question regarding the use of normal samples in ScanNeo2.
According to the information provided in the data section of the wiki, it states:
"In addition, normal allows to specif…
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Related to #136, can be reproduced with the same files found in there ([reproduce.zip](https://github.com/user-attachments/files/16993240/reproduce.zip)).
When using the `pcr` module in this case, …
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### User story:
As a customer, I would like to be able to analyse dna samples with raredisease,
so that I don't have to analyse my own FASTQ files.
### Acceptance criteria:
- A customer should b…
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```
http://forums.parallax.com/showthread.php?141129-Propeller-DNA-(PPUSB2)-config-f
iles.&p=1109244&viewfull=1#post1109244
Original text of the request:
Attached below are the propeller-load confi…