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It seems pretty obvious that since genetic information is encoded with four bases (a, t, g, and c) there ought to be BioBrainf*ck which can interpret a DNA sequence as a program.
ktnyt updated
4 years ago
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Thanks in part to @mellybelly @kltm @lwinfree and all the reusable data team, StringDB is now all cc-by, so we can pull a lot more data. Currently we are only ingesting the protein.links.detailed fil…
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https://redmine.apidb.org/issues/31075
EUPATH_0005001 BIIT test
EUPATH_0005002 Parental and Colon
https://redmine.apidb.org/issues/31466
EUPATH_0005006 VNI subdivision
EUPATH_0005005 genetic li…
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genetics maps is required for rmfix . but my study object is not hunman . so I can't download genetics map from website . Is rmfix only suit for hunman ,or should I make a genetic map special for my o…
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Hello,
When using variable selection method on markers, how do you calculate variance explained both genetic and phenotypic of all snps? I tried to follow the example in vignette but I am getting a…
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**What:**
- Transclusions ![[File name]], Header references ![[File#header 1]], and block references ![[File#^block]]
**current result**- syncing to Anki results in the plain text ![[File name]]…
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The distributed version of the algorithm receives results from the workers without validating their work. This is safe when one has control of all the instances running the worker nodes but it is dang…
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I can access the recombination map for a species (e.g. HomSap) using e.g.
```
species = stdpopsim.get_species("HomSap")
contig = species.get_contig("chr22")
map = contig.recombination_map
```
…
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https://www.nature.com/articles/s41588-019-0440-9
- [ ] [create a issue on datahub](https://github.com/cBioPortal/datahub/issues/new) before curating a study (one issue per study) and copy this che…
jjgao updated
2 years ago
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Dear beloved OpenMole and mgo developed,
When using NSGA2, [the doc ](https://next.openmole.org/Genetic+Algorithms.html) suggests the usage of the hook `SavePopulationHook` to export the population…