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Hier von MoLGen Variante erben und die markierten Felder als weitere Felder zu component dazuslicen
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#### What data file(s) does this issue pertain to?
`cnv-controlfreec-tumor-only.tsv.gz`
#### What release are you using?
v13-v15
#### Put your question or report your issue here.
The st…
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When trying to run `cnv_facets.R -h`, I get the error:
```
Error: package or namespace load failed for ‘ggplot2’ in loadNamespace(j 1.0.1 is required
Execution halted
```
When I run
```
(fa…
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Hello, is there a way to show some confidence levels for the CNV output instead of only 0, 1, and 2, like some probabilities based on the read coverage at each site? Thanks!
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Dear Team,
Thank you for developing awesome tool. I have one question regarding reported CNVs by Spectre. I was checking some reported CNVs in my dataset in the DGV database. I can see, coordinates a…
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Hello,
Thank you for providing your tool for calling CNVs from Visium data!
I am currently attempting to rerun the analysis for the dataset used in your publication (Patient 4 Rep1). Based on th…
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Thank you very much for your research in the field of CNA analysis. I have encountered some issues while using CalicoST. When I executed cellsnp-lite with three samples (10x Genomics Visium v2), the o…
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There is a significant difference in depth between the two samples in this interval, why is it the simila…
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Dear @tobiasrausch,
Hi. I'm Oh.
I executed the delly for Germline CNV calling.
I want to ask about the genotype of my called CNVs (c1.cnv.bcf), or merge the calls (merged.bcf).
```
re…
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### If you are filing this issue based on a specific GitHub Discussion, please link to the relevant Discussion.
_No response_
### Describe the goals of the changes to the analysis module.
In …