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Hi,
I have a question about annotating with dbSNP. You write that you use dbSNP and gnomAD to annotate common variants, so do you filter dbSNP variants in advance for the ones that are not rare? Beca…
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Especially for rare variants, the age distribution graph is frequently empty (for example: https://gnomad.broadinstitute.org/variant/1-55505483-C-G). In these cases, a message should be shown "Age dat…
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Interop Contact:
Active in 2021: Active
**Researchers**: Xihong Lin (Harvard T.H. Chan School of Public Health)
## Analysis Question:
Large-scale Whole Genome Sequencing (WGS) studies and biobanks h…
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Been trying to install LineageOS on my old Samsung Galaxy S5, but apparently I've got myself a rare variant of it... SM-S902L.
Tried to use the program but it came up with "Failed to load config de…
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Over 20 variants for the biomes.
M - Biomes with an M variant are much rarer than any other variant. Those are more mountainous versions of their normal biome counterpart.
- [x] Extreme Hills M
- […
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This isn't a code based question. In the homework it states:
Extract the AF_EXAC data to determine the rarity of the variant
If the disease is rare:
return an a list of associated diseases
I…
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## Description
Automatic uuid generation (happening on the fly during read requests) breaks content folder when directory name is changed via `changeStatus`.
## To reproduce
A panel request l…
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Fonts available in https://fonts.google.com/ can be selected with various filters.
But some filters are still missing to locate rare fonts that are useful for advanced typography.
Notably there'…
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Hi, when I want to add annotations to my gds file, I got this error.
Could you help me to solve this?
Warning messages:
1: In add.gdsn(ans, nm[i], val[[i]], compress = compress, closezip = closez…
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**https://github.com/sars-cov-2-variants/lineage-proposals/issues**
To reduce the amount of work and to keep this page readable, we in the variant spotters community have set up via the impulse and…