Browse data: Bioinformatics application
Choose a category:
Bioinformatics application > Operating system :
Linux or
Mac OS X; x86 64 or
Windows 7 or Higher
& Technology :
All or
Sanger
Click on one or more items below to narrow your results.
Subcategory: Missing email (17)
Ab-initio gene prediction (1) ·
Adapter removal (1) ·
Annotation (5) ·
Bisulfite mapping (1) ·
Chromatogram visualisation (1) ·
Collapsing methods (1) ·
Comparative genomics (2) ·
DNA barcoding (1) ·
Gene expression analysis (1) ·
Genome visualisation (3) ·
Graph reduction (1) ·
Heat map generation (1) ·
Hidden Markov Model (1) ·
K-mer counting (1) ·
Learning algorithm (1) ·
Local sequence alignment (2) ·
PCR primer design (1) ·
Peak calling (1) ·
Read mapping (7) ·
SNP calling (2) ·
Scaffolding (1) ·
Sequence alignment (8) ·
Sequence alignment analysis (1) ·
Sequence alignment visualisation (2) ·
Sequence analysis (5) ·
Sequence assembly (10) ·
Sequence assembly (de-novo assembly) (2) ·
Sequence assembly validation (2) ·
Sequence assembly visualisation (2) ·
Sequence contamination filtering (1) ·
Sequence error correction (1) ·
Sequence motif discovery (1) ·
Sequence parsing (1) ·
Sequencing quality control (1) ·
Statistical calculation (1) ·
Variant calling (4) ·
Variant classification (1) ·
Visualisation (5) ·
Workflows (1)
ChIP-seq (2) ·
Community analysis (2) ·
Comparative genomics (2) ·
Copy number estimation (1) ·
Data handling (2) ·
Epidemiology (1) ·
Epigenomics (2) ·
Exome analysis (1) ·
Exome and whole genome variant detection (1) ·
Gene expression analysis (1) ·
Genetic variation (1) ·
Genetics (1) ·
Genomics (13) ·
Genotyping (2) ·
Indel detection (3) ·
Mapping (2) ·
Metagenomics (4) ·
Microbial Surveillance (1) ·
Next Generation Sequencing (2) ·
Personalised medicine (1) ·
Phylogenetics (5) ·
Population genetics (1) ·
Protein structure analysis (2) ·
Quality control (1) ·
RNA-Seq (4) ·
RNA-Seq alignment (1) ·
Rarefaction (1) ·
Regulatory RNA (1) ·
SNP detection (5) ·
Sequence alignment (1) ·
Sequence analysis (8) ·
Sequence assembly (1) ·
Sequence assembly (de novo assembly) (8) ·
Sequencing (2) ·
Structural variation (2) ·
Transcription factors and regulatory sites (1) ·
Transcriptomics (3) ·
Whole genome resequencing (5) ·
Workflows (1)
Showing below up to 22 results in range #1 to #22.
View (previous 250 | next 250) (20 | 50 | 100 | 250 | 500)