|
3 | 3 | "category": "VARIANT_CALLING", |
4 | 4 | "description": "Identify nucleotide polymorphisms and short indels from Illumina and Element data.", |
5 | 5 | "name": "Variant calling", |
| 6 | + "showComingSoon": true, |
6 | 7 | "workflows": [ |
7 | 8 | { |
8 | 9 | "parameters": [ |
|
82 | 83 | "category": "TRANSCRIPTOMICS", |
83 | 84 | "description": "Analyze bulk or single-cell RNA seq data using a variety of approaches.", |
84 | 85 | "name": "Transcriptomics", |
| 86 | + "showComingSoon": true, |
85 | 87 | "workflows": [ |
86 | 88 | { |
87 | 89 | "parameters": [ |
|
157 | 159 | "category": "REGULATION", |
158 | 160 | "description": "Workflows for the analysis of ChIP-seq, ATAC-Seq, and beyond.", |
159 | 161 | "name": "Regulation", |
| 162 | + "showComingSoon": true, |
160 | 163 | "workflows": [ |
161 | 164 | { |
162 | 165 | "parameters": [ |
|
224 | 227 | "category": "CONSENSUS_SEQUENCES", |
225 | 228 | "description": "Build consensus sequences for related isolates.", |
226 | 229 | "name": "Consensus sequences", |
| 230 | + "showComingSoon": false, |
227 | 231 | "workflows": [ |
228 | 232 | { |
229 | 233 | "parameters": [ |
|
244 | 248 | "category": "ASSEMBLY", |
245 | 249 | "description": "Assemble prokaryotic and eukaryotic genomes sequenced with a variety of technologies.", |
246 | 250 | "name": "Assembly", |
| 251 | + "showComingSoon": false, |
247 | 252 | "workflows": [] |
248 | 253 | }, |
249 | 254 | { |
250 | 255 | "category": "GENOME_COMPARISONS", |
251 | 256 | "description": "Workflows for creation of pairwise and multiple genome alignments.", |
252 | 257 | "name": "Genome comparisons", |
| 258 | + "showComingSoon": true, |
253 | 259 | "workflows": [] |
254 | 260 | }, |
255 | 261 | { |
256 | 262 | "category": "PROTEIN_FOLDING", |
257 | 263 | "description": "Analysis of protein folding using the ColabFold framework.", |
258 | 264 | "name": "Protein folding", |
| 265 | + "showComingSoon": true, |
259 | 266 | "workflows": [] |
260 | 267 | } |
261 | 268 | ] |
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