-
-
Pending https://github.com/ga4gh/vrs/pull/418, and updates to VRS-Python and then the Variation Normalizer (https://github.com/cancervariants/variation-normalization/issues/394).
We'll probably nee…
-
Hi Whatshap team,
I am trying to phase haplotypes on some tetraploid potato datasets, but copy-number variation is widely distributed throughout the genome and thus I'm having issues running whatshap…
-
**Goal: Predict large duplications/amplifications.**
How?
**Update/complete existing circular binary segmentation code (C++)**
and/or
**Implement a function that compares across multiple output…
-
Roadmap:
- [ ] Find a fitting tool
- [ ] Write an example script
- [ ] Integrate the script to the pipeline
-
```
At the moment, the ontology assumes that there are two copies of each allele.
This is not necessarily the case for some pharmacogenetic alleles, where copy
number variation is relatively common …
-
```
At the moment, the ontology assumes that there are two copies of each allele.
This is not necessarily the case for some pharmacogenetic alleles, where copy
number variation is relatively common …
-
```
At the moment, the ontology assumes that there are two copies of each allele.
This is not necessarily the case for some pharmacogenetic alleles, where copy
number variation is relatively common …
-
```
At the moment, the ontology assumes that there are two copies of each allele.
This is not necessarily the case for some pharmacogenetic alleles, where copy
number variation is relatively common …
-
https://github.com/waldronlab/CNVWorkshop