Pages that link to "GeneXplain GmbH"
The following pages link to GeneXplain GmbH:
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Category:GeneXplain plugins (← links)
- Analyze SNP list (GTRD) (workflow) (← links)
- Analyze SNP list (TRANSFAC(R)) (workflow) (← links)
- Gene set enrichment analysis - select a classification (Gene table) (workflow) (← links)
- Map Transfac sites to genome (analysis) (← links)
- Apply CMA model to tracks (analysis) (← links)
- Add reactants (analysis) (← links)
- Convert identifiers for multiple gene sets (workflow) (← links)
- Quantification of RNA-seq with Cufflinks for multiple BAM files (workflow) (← links)
- Analyze any DNA sequence (GTRD) (workflow) (← links)
- Analyze any DNA sequence for site enrichment (GTRD) (workflow) (← links)
- Identify enriched motifs in promoters (GTRD) (workflow) (← links)
- Identify composite modules in promoters (TRANSFAC(R)) (workflow) (← links)
- Analyze any DNA sequence for site enrichment (TRANSFAC(R)) (workflow) (← links)
- Analyze any DNA sequence (TRANSFAC(R)) (workflow) (← links)
- Identify enriched composite modules in promoters (TRANSFAC(R)) (workflow) (← links)
- Identify enriched motifs in promoters (TRANSFAC(R)) (workflow) (← links)
- ChIP-Seq - Identify and classify target genes (TRANSPATH(R)) (workflow) (← links)
- Biouml.plugins.affymetrix (plugin) (← links)
- Analyze any DNA sequence, EMBL (workflow) (← links)
- 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)