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Package to wrangle and visualize genomic data in R

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For example, gene correlations – user gets to pick which genes to correlate (not sure what the current selection process is)

From Caroline: I’ve been considering working on these sorts of functions/smoothing out this pipeline for my own personal use. Happy to share when complete if they belong in gnomeR or...

hackathon

Functions like `summarize_by_gene()`, `susbet_by_frequency()` and `tbl_genomic()` all require a binary matrix input. These all have internal checks but we should synthesize into one input checking function (maybe `.check_gene_binary()` or `sanitize_gene_binary()`)....

future
cran

![image](https://github.com/MSKCC-Epi-Bio/gnomeR/assets/100386516/db65ff7a-742a-4ecf-afca-5530a0e7c77f) repex crc_pub % pivot_cna_wider()

pre-hackathon

Per Karissa: comparing the fusion files there are some genes with new names. We need more unit tests to make sure that this is correctly done

future

Added example heatmap under CNA_vignette **What changes are proposed in this pull request?** Added an example heatmap for copy number segmentation data **If there is an GitHub issue associated with...

incomplete

What is ggcomut measuring? Frequency? I.e. what do the numbers/colors mean? There are some white squares in the heatmap below – what do those mean compared to the tan? It’s...

hackathon

cna % mutate(alteration = recode_cna(alteration)) View(cna) View(pivot_cna_wider(cna))

1) Fusions Data - breakpointType - svStatus - variantClass - sometimes in fusions, site 1 is non impact gene but site 2 is impact gene (e.g. gnomeR::sv SHBG-TP53) - what...