Merge pull request #3117 from galaxyproject/create-pull-request/patch

metadata/feedback.csv

@@ -1534,3 +1534,8 @@
 2372,5,,,,Mapping,Sequence analysis,2021-12,2021-12-08
 2373,5,You iluustrated the principles of each analysis step.,I am not sure where I can find the codes for practice.,,Visualization of RNA-Seq results with heatmap2,Transcriptomics,2021-12,2021-12-10
 2374,5,,,,Mapping,Sequence analysis,2021-12,2021-12-13
+2375,2,was well explained. ,The tutorial looks nothing like what is one my galaxy web instance. Jupiter notebooks are not listed under visualizations but rather are under tools. The dialog that comes up when I launch Jupyter also does not look like what is in this tutorial. I can't figure it out based on what you have shown.,,Use Jupyter notebooks in Galaxy,Using Galaxy and Managing your Data,2021-12,2021-12-15
+2376,5,Well detailed method of ChIPseq and associated explanations,"The title in itself doesn't really reflect the final results of the tutorial, with the data used one do not really identify TAD on the inactive X chromosome... ",,Formation of the Super-Structures on the Inactive X,Epigenetics,2021-12,2021-12-16
+2377,4,,,,Formation of the Super-Structures on the Inactive X,Epigenetics,2021-12,2021-12-17
+2378,5,,,,Metatranscriptomics analysis using microbiome RNA-seq data,Metagenomics,2021-12,2021-12-20
+2379,1,,,,High Throughput Molecular Dynamics and Analysis,Computational chemistry,2021-12,2021-12-20