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The result of compare_genes_within_state_graph() can return NAs in the genes_within_cell_group column. This creates two issues. The first is that when I try to print the result, it prints a massive wall of data rather than the tidy tibble it is supposed to be. The second is that I get the following error when I run calculate_dvegs():
> dvegs <- calculate_dvegs(perturb_degs, degs, sig_p_val_thresh = 0.05)
Error in `list_unchop()`:
! Can't combine `x[[1]]` <grouped_df> and `x[[9]]` <character>.
Run `rlang::last_trace()` to see where the error occurred.
> rlang::last_trace()
<error/vctrs_error_ptype2>
Error in `list_unchop()`:
! Can't combine `x[[1]]` <grouped_df> and `x[[9]]` <character>.
---
Backtrace:
▆
1. ├─platt::calculate_dvegs(perturb_degs, degs, sig_p_val_thresh = 0.05)
2. │ └─perturb_degs %>% tidyr::unnest(genes_within_cell_group)
3. ├─tidyr::unnest(., genes_within_cell_group)
4. └─tidyr:::unnest.data.frame(., genes_within_cell_group)
5. └─tidyr::unchop(...)
6. └─tidyr:::df_unchop(...)
7. └─vctrs::list_unchop(col, ptype = col_ptype)
Run rlang::last_trace(drop = FALSE) to see 9 hidden frames.
If I filter out the NA columns from the perturb DEGs, it works fine:
dvegs <- calculate_dvegs(perturb_degs %>% filter(!is.na(genes_within_cell_group)), degs, sig_p_val_thresh = 0.05)Either compare_genes_within_state_graph() should fill in the NAs better/filter them out so the user's console isn't flooded with text, or calculate_dvegs() should have a filtering step at the very beginning.
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