Browse data: Bioinformatics application
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Bioinformatics application > Operating system :
Linux or
UNIX
& Technology :
Anything that can be assembled with Celera or Newbler or
Sanger
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Subcategory: Missing email (27)
C (6) ·
C++ (12) ·
Fortran (1) ·
GO (1) ·
Java (6) ·
JavaScript (1) ·
Perl (10) ·
Pilot Script (1) ·
Python (1) ·
R (1) ·
Tcl (1)
Ab-initio gene prediction (1) ·
Adapter removal (1) ·
Annotation (4) ·
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 (2) ·
Learning algorithm (1) ·
Local sequence alignment (3) ·
Mapping (1) ·
Modelling and simulation (1) ·
RRNA filtering (1) ·
Read mapping (9) ·
Read pre-processing (2) ·
SNP calling (2) ·
Sequence alignment (6) ·
Sequence alignment visualisation (2) ·
Sequence analysis (4) ·
Sequence assembly (10) ·
Sequence assembly (de-novo assembly) (2) ·
Sequence assembly validation (2) ·
Sequence assembly visualisation (2) ·
Sequence contamination filtering (3) ·
Sequence error correction (1) ·
Sequence motif discovery (1) ·
Sequence parsing (1) ·
Sequence trimming (2) ·
Sequencing quality control (1) ·
Statistical calculation (1) ·
Variant calling (3) ·
Variant classification (1) ·
Visualisation (5)
ChIP-seq (2) ·
Community analysis (2) ·
Comparative genomics (1) ·
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 (18) ·
Genotyping (1) ·
Indel detection (2) ·
Mapping (4) ·
Metabolic reconstruction (1) ·
Metagenomics (9) ·
Next Generation Sequencing (2) ·
Personalised medicine (1) ·
Phylogenetics (6) ·
Population genetics (1) ·
Protein structure analysis (1) ·
RNA-Seq (4) ·
RNA-Seq alignment (1) ·
Rarefaction (1) ·
Regulatory RNA (1) ·
SNP detection (5) ·
Sequence alignment (1) ·
Sequence analysis (7) ·
Sequence assembly (de novo assembly) (7) ·
Sequencing (3) ·
Structural variation (2) ·
Transcriptomics (7) ·
Whole genome resequencing (4)
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