-
The gene is displayed on the geneS overview:
But when you click on the gene the page crashes ->
Note that GAREM gene has been renamed to GAREM1, so perhaps the link to gene page should u…
-
Hi, I've generated contact heatmaps successfully from mcool files.
I wonder if there is a way to add gene annotations to the generated heatmaps?
-
Right now, the gene page takes a minute or so to load. This becomes unfeasible when working through a list of many partially covered genes.
Testing it out, it took ~3 minutes for one gene to load:
…
-
**Priority**: high
@bschilder will provide lists of genes driving the association between each significant phenotype-cell type association (ie genes in both lists with the highest specificity quant…
-
I come across this issue many times when I have two Anndata objects A and B and I want to change B to have the same vars as A by keeping the shared genes and inflating the new genes that are in A but …
-
**Describe the issue**
I am running the latest version of kb_python to reproduce the example pipeline in the BIVI paper (which was using an older version of kb_python). I generated the loom successf…
-
From Barry:
> was unable to review the gene TNN. When I would type that gene symbol in the app I would get a drop down with many possible completions, but all of the completions available were parti…
-
Hi @EricKutschera
When I ran ESPRESSO, the abundance file reported around 13,000 genes, but rmats-long produced a `differential_genes.tsv` file with only 9,800 genes. I'm a bit confused about how …
-
Optionally, have the predictor return a data frame with missing genes (if any, and `impute = TRUE`). This would allow the user to have a backtrace of their runs.
-
Dear Developer, Can I use TOGA to find out the missing and added genes in the query sequence relative to the reference sequence?If so, which result file should I look at?