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### Description
This excerpt, as well as others in the article Mamba: Linear-Time Sequence Modeling with Selective State Spaces, have rendering errors
### (Optional:) Please add any files, screensho…
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~~Please add a column in the dashboard download file that includes the URL link to the curation in the VCI/GCI~~ Released 12/18/2023
Other requests:
1. ~~Please add a column with the CAID in the d…
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VariantSpark is currently optimised for reasonally small sample sizes (n=100-5000) and large numbers of variants (e.g. 42 million) , ie. 'wide' datasets. Working on phenotypes in UKBB, e.g. CAD we hav…
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**Describe the bug**
There is something fishy with `NM_030582.4`. Take, e.g., this deletion that maps to this transcript: [`NC_000021.8:g.46924426_46924427del`](https://variantvalidator.org/service/v…
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Not really an issue, just showing some performance metrics of `hifiasm` with a simulated diploid assembly of the T2T chr8 sequence, with simulated PacBio HiFi reads. Used default `hifiasm` settings ex…
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For example, from the server test data:
```
va.transcriptEffects[0].hgvsAnnotation.toJsonDict()
```
gives
```
{u'genomic': u'1:g.46286_46288delTAT',
u'protein': u'',
u'transcript': u'n.46286_462…
reece updated
7 years ago
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As per @richarddurbin 's discussion today, which of these models do we want to use for representing variants?
Right now, we (and VCF) have a multiallelic model. Many databases, however, like Genomics…
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Currently we have pages for specific variants, but if you want to find variants of interest, you are restricted to either (1) autocomplete searches on label or (2) finding another entity of interest (…
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Currently, LOVD is very gene-centered. When a gene is selected, the user gets shortcuts to several gene-specific overviews (e.g. all diseases associated with that gene, or all unique variants in that …
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![bild](https://user-images.githubusercontent.com/12525201/74742279-98ab7b80-525e-11ea-98c7-269f5820f444.png)
the mutation is true positive, but it is NOT a mosaic.
Can the tag be moved in anothe…