Browse data: Bioinformatics application
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Bioinformatics application > Language :
Pilot Script or
Other
& Technology :
Anything that can be assembled with Celera or Newbler or
Sanger
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Subcategory: Missing email (30)
Ab-initio gene prediction (1) ·
Adapter removal (1) ·
Annotation (4) ·
Base-calling (2) ·
Bisulfite mapping (1) ·
Comparative genomics (1) ·
DNA barcoding (1) ·
Gene expression analysis (1) ·
Genome visualisation (1) ·
Graph reduction (1) ·
Heat map generation (1) ·
Hidden Markov Model (1) ·
K-mer counting (2) ·
Learning algorithm (1) ·
Local sequence alignment (2) ·
Mapping (2) ·
Modelling and simulation (2) ·
Peak calling (1) ·
RNA-Seq analysis (1) ·
RRNA filtering (1) ·
Read mapping (13) ·
Read pre-processing (2) ·
SNP calling (2) ·
Sequence alignment (8) ·
Sequence alignment visualisation (2) ·
Sequence analysis (4) ·
Sequence assembly (13) ·
Sequence assembly (de-novo assembly) (2) ·
Sequence assembly validation (2) ·
Sequence assembly visualisation (1) ·
Sequence contamination filtering (3) ·
Sequence error correction (1) ·
Sequence motif discovery (1) ·
Sequence parsing (1) ·
Sequence trimming (2) ·
Statistical calculation (1) ·
Variant calling (4) ·
Visualisation (6) ·
Workflows (1)
Alternative splicing (1) ·
ChIP-seq (3) ·
Clone verification (1) ·
Community analysis (2) ·
Comparative genomics (2) ·
Epigenomics (1) ·
Gene expression analysis (1) ·
Genetic variation (1) ·
Genomics (20) ·
Genotyping (1) ·
Indel detection (3) ·
Mapping (4) ·
Metabolic reconstruction (1) ·
Metagenomics (10) ·
Microbial Surveillance (1) ·
Next Generation Sequencing (1) ·
Personalised medicine (1) ·
Phylogenetics (7) ·
Population genetics (1) ·
Protein structure analysis (1) ·
Quality control (1) ·
RNA-Seq (4) ·
RNA-Seq alignment (2) ·
Rarefaction (1) ·
Read binning (1) ·
Regulatory RNA (1) ·
Resequencing (1) ·
SNP detection (5) ·
Sequence alignment (1) ·
Sequence analysis (6) ·
Sequence assembly (de novo assembly) (6) ·
Sequencing (3) ·
Structural variation (2) ·
Transcriptomics (6) ·
Whole genome resequencing (4)
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