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Compound heterozygous mode is when there are two variants in the same gene, but not at the same genomic position.
![capture du 2017-11-04 14-55-19](https://user-images.githubusercontent.com/5510283/3…
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Just always use regular round-bracket parentheses.
HOME [tab] > Explore genomic data through the Viewer [heading] > View genome [button] > Variants [channel] > [cog button] > [channel configuration] …
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Preethi to share Xref Template from GlyGen-ProtVar
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Request/Suggestion from a user: It would be useful to be able to navigate to a position relative to the start of a feature. For example: Go to the 10th nucleotide of transcript X. This is because ofte…
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(Maybe hide the "Default filter" button when it is "No filter".)
HOME [tab] > Explore genomic data through the Viewer [heading] > View genome [button] > Variants [channel] > [cog button] > [channel c…
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With #754 we're halfway to also supporting inframe indels so we should just do the rest of the work necessary to support those types of proximal variants.
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As an example, (I hope that this Scout-link will persist): https://scout-stage.scilifelab.se/cust087/F0049453/sv/variants/8e2113f40646b16473f9a12af4e57e0b
This is one of the variants that we're loo…
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HOME [tab] > Explore genomic data through the Viewer [heading] > View genome [button] > Variants [channel] > [cog button] > [channel configuration] > ADD FILTER [button] > [dialog]
(Maybe only allow …
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### Need
As a geneticist I want to see true variants and not false positive calls. Currently we have databases for annotating variants that are commonly observed as somatic in highly filtered T+N c…
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**Background**:
OncoKB™(https://www.oncokb.org) is a precision oncology knowledge base developed at Memorial Sloan Kettering Cancer Center that contains biological and clinical information about gen…