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**Description**
**Sub-lineage of:** BA.2
**Earliest sequence:** 2024-7-14, Spain – EPI_ISL_19322462
**Most recent sequence:** 2024-7-16, Spain – EPI_ISL_19370418
**Continents circulating:** Europe…
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Hello,
I would like to thank you for such an incredible and well-documented resource, which is way better than the DNAnexus'es own pipelines/instructions. I was wondering if you have figured how to …
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I can't find an issue for this, though it came up in the [Mischievous Nominals paper](https://aclanthology.org/2021.udw-1.14) - example (5):
- **We** pilots deserve a pay raise
- **You** guys dese…
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Hello, I was performing the rare variant analysis using the sliding window approach. When running the pre-built pipeline, I have several questions that need your help. Thank you!
1. For each loop i…
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Dear raremetal developers,
I really appreciate the work you are doing to develop and maintain raremetal. I am reaching out because I need some help to understand raremetal behaviour.
Recently, I…
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Dear,
I still felt confused about how to obtain the NO.case and NO.control. You said that " (No.case, how many times the variant appears in cases, No.contr, how many times the variant appears …
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I can succesfully run the glmm.score model, but when i run the SMMAT command, it output partial results and reported the error:
**Error in if (n.p == 0) next : missing value where TRUE/FALSE needed
…
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First step is to figure out which services are offered for each provider. We should look at each product as well, in case the analysis services also differ by product.
- [ ] Nebula Genomics
- [x] …
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Hello!
I am getting an error when I try to annotate a VCF file which is based on hg19.
You can find the vcf file and the log file in the given URL:
```
https://drive.google.com/drive/folders/1…
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Hi,
I am a Human Genetics PhD student in South Africa and we are doing a project looking at CNVs in Sub-Saharan African individuals. We have run GenomeSTRiP on ~1000 samples and looking at the output…