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### Operating System
Other Linux (please specify below)
### Other Linux
ubuntu 20
### Workflow Version
v.1.8.3
### Workflow Execution
Command line
### EPI2ME Version
_No response_
### CLI co…
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貼吧活動:(請查閱 [SARS-CoV-2 Timeline by 2020.02.21](https://github.com/agorahub/_meta/blob/agoran/theagora/sari/Memorandum_2020-02-21_SARS-CoV-2-Timeline_Nathan.pdf?raw=true), by Nathan :cloud: )
- Colla…
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```R
library(gwasrapidd)
child_traits
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Hello!
First I want to say thank you for maintaining this awesome software :)
I have a question regarding the input VCF format when using snpgenie.pl.
For context, I am interested in analyzi…
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# Combined Annotation Dependent Depletion (CADD)
- [ CADD is a tool for scoring the deleteriousness of single nucleotide variants as well as insertion/deletions variants in the human genome. ](https…
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Hello,
I am running SvAnna for prioritization of short-read variants from MetaSV output. While I am getting an output in both the noted formats, the HTML format is not prioritizing any variants th…
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**Describe the bug**
Annotation of large insertions derived from structural variants is not performed if a symbollic allele is used like `` but it is performed if the sequence is present in the ALT f…
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## Description
TNscope VCF is missing GQ-values. Therefore, SNVs are not being uploaded to the `loqusdb-somatic` database.
It has been solved in Loqusdb side in https://github.com/Clinical-Geno…
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Submitting Author: Remy Tuyeras (@remytuyeras)
Package Name: HaploDynamics
One-Line Description of Package: A python library to develop genomic data simulators
Repository Link (if existing): ht…
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Dear BHR team,
Thanks for developing such a useful tool! As I try to make sense of my own analysis, I wonder if it is reasonable to apply the bivariate mode of BHR to evaluate the correlation betwe…