Browse data: Bioinformatics application
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Bioinformatics application > Operating system :
Linux or
Linux 64
& Technology :
Anything that can be assembled with Celera or Newbler or
Sanger
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Subcategory: Missing email (18)
C (2) ·
C++ (9) ·
Fortran (1) ·
Java (7) ·
JavaScript (1) ·
PHP (1) ·
Perl (6) ·
Pilot Script (1) ·
R (1) ·
Tcl (1)
Ab-initio gene prediction (1) ·
Adapter removal (1) ·
Annotation (3) ·
Base-calling (1) ·
Bisulfite mapping (1) ·
Collapsing methods (1) ·
Comparative genomics (1) ·
DNA barcoding (1) ·
Gene expression analysis (1) ·
Genome visualisation (2) ·
Graph reduction (1) ·
Heat map generation (1) ·
Hidden Markov Model (1) ·
K-mer counting (1) ·
Learning algorithm (1) ·
Local sequence alignment (2) ·
Read mapping (8) ·
SNP calling (2) ·
Sequence alignment (7) ·
Sequence alignment visualisation (2) ·
Sequence analysis (4) ·
Sequence assembly (11) ·
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)
ChIP-seq (2) ·
Clone verification (1) ·
Community analysis (2) ·
Comparative genomics (2) ·
Copy number estimation (1) ·
Data handling (1) ·
Epigenomics (2) ·
Exome analysis (1) ·
Exome and whole genome variant detection (1) ·
Gene expression analysis (1) ·
Genetic variation (1) ·
Genetics (1) ·
Genomics (12) ·
Genotyping (1) ·
Indel detection (2) ·
Mapping (1) ·
Metagenomics (4) ·
Microbial Surveillance (1) ·
Next Generation Sequencing (2) ·
Personalised medicine (1) ·
Phylogenetics (4) ·
Population genetics (1) ·
Protein structure analysis (1) ·
RNA-Seq (4) ·
RNA-Seq alignment (1) ·
Rarefaction (1) ·
Regulatory RNA (1) ·
SNP detection (4) ·
Sequence alignment (1) ·
Sequence analysis (6) ·
Sequence assembly (de novo assembly) (8) ·
Sequencing (4) ·
Structural variation (2) ·
Transcriptomics (3) ·
Whole genome resequencing (4)
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