Enrichr links; References; Clustergrammer

Author: maxim-k

appyters/Bulk_RNA_seq/RNA_seq_Analysis_Pipeline.ipynb

@@ -815,6 +815,7 @@
     "    enrichr_link_dict[title_down] = dict()\n",
     "    enrichr_link_dict[title_down][\"link\"] = \"<a href=https://maayanlab.cloud/Enrichr/enrich?dataset={} target=\\\"_blank\\\">link to Enrichr</a>\".format(results['enrichr'][label][\"downregulated\"][\"shortId\"])\n",
     "\n",
+    "notebook_metadata['enrichr_links'] = enrichr_link_dict\n",
     "enrichr_link_df = pd.DataFrame.from_dict(enrichr_link_dict).T\n",
     "table_counter, notebook_metadata = display_object(table_counter, \"The table displays links to Enrichr containing the results of enrichment analyses generated by analyzing the up-regulated and down-regulated genes from a differential expression analysis. By clicking on these links, users can interactively explore and download the enrichment results from the Enrichr website.\", notebook_metadata=notebook_metadata, saved_filename=\"enrichr_links.csv\", df=enrichr_link_df, ishtml=True)"
    ]

appyters/Bulk_RNA_seq/appyter.json

@@ -2,7 +2,7 @@
   "$schema": "https://raw.githubusercontent.com/MaayanLab/appyter-catalog/main/schema/appyter-validator.json",
   "name": "Bulk_RNA_seq",
   "title": "Bulk RNA-seq analysis pipeline",
-  "version": "0.1.8",
+  "version": "0.1.9",
   "description": "Bulk RNA-seq analysis pipeline enables you to analyze and visualize datasets with state-of-the-art algorithms and visualization methods.",
   "image": "screenshot.png",
   "authors": [
@@ -16,7 +16,7 @@
     },
     {
       "name": "Maxim Kuleshov",
-      "email": "kuleshov.max.v@gmail.com"
+      "email": "maxim.kuleshov@mssm.edu"
     }
   ],
   "url": "https://github.com/MaayanLab/appyter-catalog",

appyters/Bulk_RNA_seq/utils.py

@@ -924,7 +924,7 @@ def plot_l1000cds2(l1000cds2_results, counter, notebook_metadata, nr_drugs=7, he
 
     else:
         # Bar charts
-        fig = tools.make_subplots(rows=1, cols=2, print_grid=False)
+        fig = tools.make_subplots(rows=1, cols=2, print_grid=False);
         for i, direction in enumerate(['mimic', 'reverse']):
             drug_counts = l1000cds2_results[direction]['table'].groupby('pert_desc').size().sort_values(
                 ascending=False).iloc[:nr_drugs].iloc[::-1]
@@ -969,17 +969,22 @@ def plot_l1000cds2(l1000cds2_results, counter, notebook_metadata, nr_drugs=7, he
             fig.show()
         else:
             fig.show(renderer="png")
-        
-        counter, notebook_metadata = display_object(counter, "Top {} Mimic/Reverse Small Molecule from L1000CDS2 for {}.".format(nr_drugs, l1000cds2_results['signature_label']), notebook_metadata, saved_filename=plot_name, istable=False)
-        notebook_metadata["figures"][str(counter-1)]["file_desc"] = [{"name": "Mimic Signature Query Results", "link":l1000cds2_results['mimic']['url']},
-                                                                     {"name": "Reverse Signature Query Results", "link":l1000cds2_results['reverse']['url']},]
-        
-        # Links        
+
+
+        counter, notebook_metadata = display_object(counter,
+                                                    "Top {} Mimic/Reverse Small Molecule from L1000CDS2 for {}.".format(
+                                                        nr_drugs, l1000cds2_results['signature_label']),
+                                                    notebook_metadata, saved_filename=plot_name, istable=False)
+        notebook_metadata["figures"][str(counter - 1)]["file_desc"] = [
+            {"name": "Mimic Signature Query Results", "link": l1000cds2_results['mimic']['url']},
+            {"name": "Reverse Signature Query Results", "link": l1000cds2_results['reverse']['url']}, ]
+
+        # Links
         display(Markdown(' *Mimic Signature Query Results*:'))
         display_link(l1000cds2_results['mimic']['url'])
         display(Markdown(' *Reverse Signature Query Results*:'))
         display_link(l1000cds2_results['reverse']['url'])
-        
+
     return counter, notebook_metadata
 
 def run_l1000fwd(signature, nr_genes=500, signature_label=''):