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Full overlap of + and - gene sets detected and suggested to increase number of marker genes for scoring #5
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Hi! Thanks alot for giving it ago! You can bypass this exception by:
I had the default behaviour to throw this exception, to flag there were no marker gene differences between two clusters, and that perhaps increasing the number of marker genes could reveal an additional gene that would differentiate the clusters. I suppose you can try both approaches (increase marker genes and squash_exception=True) to see if it changes the results. |
Hi, thank you very much for your quick reply! I've tried both (increase marker genes to 50 and squash_exception=True), but there's a different issue ---------------------------------------------------------------------------
ValueError Traceback (most recent call last)
Cell In[53], line 1
----> 1 cc.tl.merge_clusters(rna, new_anno, n_cpus=4, squash_exception=True)
File [/work/home/software/anaconda3/envs/scanpy/lib/python3.10/site-packages/cytocipher/score_and_merge/cluster_merge.py:580](https://app-5085186-0.cloud.sdu.dk/lab/tree/DevM_analysis/01.annotation/11.subclustering/HSC/home/software/anaconda3/envs/scanpy/lib/python3.10/site-packages/cytocipher/score_and_merge/cluster_merge.py#line=579), in merge_clusters(data, groupby, var_groups, n_top_genes, t_cutoff, marker_padj_cutoff, gene_order, min_de, enrich_method, p_cut, max_iter, mnn_frac_cutoff, k, random_state, n_cpus, score_group_method, p_adjust, p_adjust_method, squash_exception, verbose)
574 get_markers(data, f'{groupby}_merged', n_top=n_top_genes, verbose=False,
575 var_groups=var_groups, t_cutoff=t_cutoff,
576 padj_cutoff=marker_padj_cutoff,
577 gene_order=gene_order, min_de=min_de)
579 # Running the enrichment scoring #
--> 580 run_enrich(data, f'{groupby}_merged', enrich_method, n_cpus,
581 squash_exception=squash_exception)
583 if verbose:
584 print(f"Added data.obs[f'{groupby}_merged']")
File [/work/home/software/anaconda3/envs/scanpy/lib/python3.10/site-packages/cytocipher/score_and_merge/cluster_merge.py:419](https://app-5085186-0.cloud.sdu.dk/lab/tree/DevM_analysis/01.annotation/11.subclustering/HSC/home/software/anaconda3/envs/scanpy/lib/python3.10/site-packages/cytocipher/score_and_merge/cluster_merge.py#line=418), in run_enrich(data, groupby, enrich_method, n_cpus, squash_exception)
415 raise Exception(
416 f"Got enrich_method={enrich_method}; expected one of : {enrich_options}")
418 if enrich_method == 'code':
--> 419 code_enrich(data, groupby, n_cpus=n_cpus, verbose=False,
420 squash_exception=squash_exception)
421 elif enrich_method == 'coexpr':
422 coexpr_enrich(data, groupby, n_cpus=n_cpus, verbose=False)
File [/work/home/software/anaconda3/envs/scanpy/lib/python3.10/site-packages/cytocipher/score_and_merge/cluster_score.py:593](https://app-5085186-0.cloud.sdu.dk/lab/tree/DevM_analysis/01.annotation/11.subclustering/HSC/home/software/anaconda3/envs/scanpy/lib/python3.10/site-packages/cytocipher/score_and_merge/cluster_score.py#line=592), in code_enrich(data, groupby, cluster_marker_key, n_cpus, min_counts, squash_exception, verbose)
590 [all_genes.extend(cluster_genes_dict[cluster])
591 for cluster in cluster_genes_dict]
592 # Getting correct typing
--> 593 str_dtype = f"<U{max([len(gene_name) for gene_name in all_genes])}"
594 all_genes = np.unique( all_genes ).astype(str_dtype)
596 str_dtype_clust = f"<U{max([len(clust) for clust in cluster_genes_dict])}"
ValueError: max() arg is an empty sequence |
Hey @YiweiNiu, this seems to be the same issue as #4. Wondering if you could try running this code snippet as I suggested in that thread:
In particular, could you send the result of all_genes? I have been using Cytocipher quite alot lately and don't get this error, so get a feeling is something dataset dependent, or perhaps an issue with the current version I have on pip. |
Hi,
Thanks for this useful tool! I tried to apply Cytocipher to my data but got an error in step
cc.tl.merge_clusters
It suggested to increase the number of marker genes for scoring. For now I'm using 15 and based on this thread, you mentioned that using 5-8 genes is appropriate. So, should I increase the number of marker genes for scoring? or is there another workaround for this?
Thnaks!
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