Browse data: Bioinformatics application
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Bioinformatics application > Language :
CUDA or
Flash or
Perl
& Operating system :
Compaq Alpha or
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Linux 64 or
Windows 7 or Higher
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Subcategory: Missing email (43)
Analysis pipeline (1) ·
Annotation (2) ·
Bisulfite mapping (2) ·
Comparative genomics (1) ·
Correlation (1) ·
De novo mutation detection (1) ·
Differential Binding (1) ·
Formatting (1) ·
Gene expression analysis (1) ·
Hidden Markov Model (1) ·
Indel detection (1) ·
Integrated solution (1) ·
K-mer counting (1) ·
Mapping (2) ·
Methylation calling (3) ·
Modelling and simulation (1) ·
Peak calling (3) ·
Read mapping (13) ·
Read pre-processing (1) ·
SNP annotation (3) ·
SNP calling (3) ·
SNP detection (2) ·
Scaffolding (2) ·
Sequence alignment (6) ·
Sequence analysis (5) ·
Sequence annotation (1) ·
Sequence assembly (10) ·
Sequence assembly (de-novo assembly) (1) ·
Sequence assembly validation (2) ·
Sequence assembly visualisation (1) ·
Sequence motif comparison (2) ·
Sequence motif discovery (2) ·
Sequence motif recognition (1) ·
Sequencing quality control (1) ·
Standardisation and normalisation (1) ·
Statistical calculation (1) ·
Variant calling (3) ·
Variant prioritisation (1) ·
Visualisation (4)
Alternative splicing (1) ·
Cancer biology (1) ·
ChIP-seq (6) ·
Clone verification (1) ·
Community analysis (2) ·
Comparative genomics (1) ·
Copy number estimation (1) ·
DNA methylation (4) ·
Data handling (1) ·
De novo mutation detection (1) ·
Epigenetics (3) ·
Epigenomics (4) ·
Gene expression analysis (1) ·
Gene regulation (1) ·
Gene structure (2) ·
Genetic variation (2) ·
Genetics (1) ·
Genomics (13) ·
Genotyping (1) ·
Indel detection (4) ·
Mapping (1) ·
Metagenomics (5) ·
Next Generation Sequencing (1) ·
Personalised medicine (1) ·
Phylogenetics (2) ·
RNA-Seq (5) ·
RNA-Seq quantification (1) ·
Rarefaction (1) ·
Regulatory RNA (1) ·
SNP (3) ·
SNP detection (4) ·
Sequence analysis (5) ·
Sequence assembly (1) ·
Sequence assembly (de novo assembly) (4) ·
Sequence motifs (1) ·
Sequencing (7) ·
Structural variation (2) ·
Transcriptomics (3) ·
Whole genome resequencing (2)
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