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Showing below up to 50 results starting with #351.
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- Jupyter (3 revisions)
- Find gene fusions from RNA-seq (workflow) (3 revisions)
- 1-dimensional arterial tree model (3 revisions)
- Genes (reference type) (3 revisions)
- Transcript structure analysis (3 revisions)
- Infer network (analysis) (3 revisions)
- Report generator for quality control analysis (3 revisions)
- Merge peaks (analysis) (3 revisions)
- Find miRNA feed forward loops with CMA (analysis) (3 revisions)
- ArticleTrackCreator (analysis) (3 revisions)
- Proteins - PDB (3 revisions)
- Isoform TE (analysis) (3 revisions)
- Drugs - DrugBank (3 revisions)
- Analyze any DNA sequence, EMBL (workflow) (3 revisions)
- Convert diagram to pairs (analysis) (3 revisions)
- Group table rows (analysis) (3 revisions)
- Create miRNA promoters (analysis) (3 revisions)
- Illumina metylation probes to track (analysis) (3 revisions)
- Reference type (3 revisions)
- Matrices (reference type) (3 revisions)
- Find genome variants and indels from RNA-seq (workflow) (3 revisions)
- Categories - ExPASy (3 revisions)
- Optimization document (3 revisions)
- Cis-module sets near given genes (analysis) (3 revisions)
- 3D viewer (3 revisions)
- Genes - BKL (3 revisions)
- Transcriptome mappability (analysis) (3 revisions)
- Copy data element (analysis) (3 revisions)
- Merge simulation results (analysis) (3 revisions)
- Select keynodes with top targets (analysis) (3 revisions)
- Find regulatory regions (analysis) (3 revisions)
- ChIP-Seq - Identify and classify target genes (TRANSPATH(R)) (workflow) (3 revisions)
- Treatment Simulation (analysis) (3 revisions)
- Identification of cis-regulatory modules with given pattern of TF-classes (analysis) (3 revisions)
- Make GTF for riboseq alignment (analysis) (3 revisions)
- Server administrator (3 revisions)
- Analyze any DNA sequence, Fasta (workflow) (3 revisions)
- Convert files to tracks (analysis) (3 revisions)
- Quality control analysis (3 revisions)
- Reference type (extension point) (3 revisions)
- KeyNodes hub (3 revisions)
- Score based FBC table builder (analysis) (3 revisions)
- Find genome variants and indels from full-genome NGS (workflow) (3 revisions)
- Site search report (analysis) (3 revisions)
- Compute differentially expressed genes (Agilent Tox probes) (workflow) (3 revisions)
- Transcriptome minimal unique length (analysis) (3 revisions)
- Merge table columns (analysis) (3 revisions)
- Bsa (host object) (3 revisions)
- Select random rows (analysis) (3 revisions)
- Sort SQL track (analysis) (3 revisions)
