Pages that link to "GeneXplain GmbH"
The following pages link to GeneXplain GmbH:
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Analyze any DNA sequence, Fasta (workflow) (← links)
- Analyze any DNA sequence, GeneBank (workflow) (← links)
- Compute differentially expressed genes (Agilent Tox probes) (workflow) (← links)
- Explain my genes (workflow) (← links)
- Compute differentially expressed genes using EBarrays (workflow) (← links)
- Compute differentially expressed genes using Limma (workflow) (← links)
- Find common effectors for multiple gene sets (GeneWays) (workflow) (← links)
- Find gene fusions from RNA-seq (workflow) (← links)
- Find genome variants and indels from RNA-seq (workflow) (← links)
- Find genome variants and indels from full-genome NGS (workflow) (← links)
- Mapping to GO ontologies and comparison for two gene sets (workflow) (← links)
- Mapping to ontology - select a classification (Gene table) (workflow) (← links)
- Mapping to ontology - select a classification (2 Gene tables) (workflow) (← links)
- Mapping to ontology - select a classification (Multiple Gene tables) (workflow) (← links)
- Prediction of miRNA binding sites (workflow) (← links)
- Quantification of RNA-seq with Cufflinks (no de-novo assembly) for FASTQ files (workflow) (← links)
- Quantification of RNA-seq with Cufflinks (with de-novo assembly) for FASTQ files (workflow) (← links)
- SRA to FASTQ (workflow) (← links)
- Find enriched TF binding sites in variation sites (TRANSFAC(R)) (workflow) (← links)
- Identify enriched motifs in tracks (TRANSFAC(R)) (workflow) (← links)
- Enriched upstream analysis (TRANSFAC(R) and TRANSPATH(R)) (workflow) (← links)
- Mapping to ontologies and comparison for two gene sets (TRANSPATH(R)) (workflow) (← links)
- Find common effectors for multiple gene sets (TRANSPATH(R)) (workflow) (← links)
- Recalculate composite module score on new track (analysis) (← links)
- Cluster by path (analysis) (← links)
- Find longest connected chains (analysis) (← links)
- Find shortest path between two sets (analysis) (← links)
- Flux Balance Analysis (workflow) (← links)
- Hypergeometric analysis for multiple inputs (workflow) (← links)
- Quantification of RNA-seq in BAM format for mouse mm9 single end (workflow) (← links)
- Quantification of RNA-seq in FASTQ format for mouse mm9 single end (workflow) (← links)
- Identify enriched composite modules in promoters (GTRD) (workflow) (← links)
- Find master regulators in networks with context genes (TRANSPATH(R)) (workflow) (← links)
- Identify enriched motifs in tissue specific tracks (TRANSFAC(R)) (workflow) (← links)
- Identify enriched motifs in tissue specific promoters (TRANSFAC(R)) (workflow) (← links)
- Cross-species identification of enriched motifs in promoters, using orthologue information (TRANSFAC(R)) (workflow) (← links)
- Find 10 master regulators in networks (TRANSPATH(R)) (workflow) (← links)
- Find master regulators in mutated network (workflow) (← links)
- Find 3 master regulators in networks with context genes (TRANSPATH(R)) (workflow) (← links)
- Focused upstream analysis (TRANSFAC(R) and TRANSPATH(R)) (workflow) (← links)
- Search for self-regulating transcription factors (TRANSFAC(R) and TRANSPATH(R)) (workflow) (← links)
- Upstream analysis with feedback loop (TRANSFAC(R) and TRANSPATH(R)) (workflow) (← links)
- CMA Result Statistic (analysis) (← links)
- Construct composite modules on track (correlation) (analysis) (← links)
- Continue CMA (analysis) (← links)
- Find miRNA feed forward loops with CMA (analysis) (← links)
- Reduce CMA results (analysis) (← links)
- Convert diagram to Transpath (analysis) (← links)
- Convert diagram to pairs (analysis) (← links)
- Diagram to user hub collection (analysis) (← links)