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Im opening this issue just to help me track some notes, and things I need to look into. This will help with #78 .
## useful references
[Kipping (2013)]: for the reparameterization of the limb…
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Hi，
May I ask whether PRScs can be used to analyze candidate genes at the level of candidate genes?
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**Submitting author:** @vyrjana (Ville Yrjänä)
**Repository:** https://github.com/vyrjana/DearEIS
**Branch with paper.md** (empty if default branch): joss-paper
**Version:** 3.4.2
**Editor:** @jgostic…
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Hi,
I performed run and add_to_seurat.
It was successful, but I couldn't understand the columns of the meta.data.
I read https://github.com/broadinstitute/infercnv/wiki/Extracting-features, but…
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I have tried to build _all_ ROS packages on Linux and it's going quite smoothly for a lot of them.
Some do need some "fixing" though (a patch here and there) and this is the list of those (some are…
wolfv updated
2 years ago
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I was trying to use inferCNV to separate tumor from non-tumor cells. I have several samples and there are definitely immune (not tumor) cells present. I did not specify any groups as reference. This w…
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Hi @all,
Appreciated the great tools to study the scRNA CNV.
I am running the inferCNV to explore the ScRNA CNV in big matrix with 106685 on columns and 35599 on rows, however,
…
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Thank you for sharing your code which is of high quality.
Do you have a link to download all the datasets used in your experiments?
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hello everyone, as discussed in a previous e-mail, I add a table containing some package that are not covered in this CRAN Task View.
I downloaded all packages Descriptions from CRAN and searched f…
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Dear NGSEP developers,
Thanks for this great tool. I'm using the `SingleSampleVariantsDetector` module to identify SNV in pool-seq data as well as single sample dataset. I was wondering if is there…