Browse data: Bioinformatics application
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Bioinformatics application > Operating system:
UNIX
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454 or
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Subcategory: Missing email (40)
C (18) ·
C++ (12) ·
CGI (1) ·
Fortran (1) ·
GO (1) ·
Java (2) ·
JavaScript (1) ·
Perl (16) ·
Python (4) ·
R (7) ·
Tcl (1)
Adapter removal (1) ·
Analysis pipeline (1) ·
Annotation (1) ·
DNA barcoding (2) ·
File reformatting (1) ·
Gene set testing (1) ·
Genome indexing (1) ·
Graph reduction (1) ·
Hidden Markov Model (1) ·
K-mer counting (2) ·
Learning algorithm (1) ·
Local sequence alignment (2) ·
Mapping (2) ·
Methylation calling (1) ·
Modelling and simulation (2) ·
Mutation detection (1) ·
RRNA filtering (1) ·
Read alignment (4) ·
Read mapping (11) ·
Read pre-processing (3) ·
Repeat sequence organisation analysis (1) ·
Sequence alignment (3) ·
Sequence alignment analysis (2) ·
Sequence alignment visualisation (1) ·
Sequence analysis (3) ·
Sequence assembly (6) ·
Sequence contamination filtering (5) ·
Sequence error correction (1) ·
Sequence motif comparison (1) ·
Sequence motif discovery (1) ·
Sequence motif recognition (1) ·
Sequence redundancy removal (1) ·
Sequence trimming (4) ·
Sequencing quality control (5) ·
Statistical calculation (3) ·
Variant calling (4) ·
Variant prioritisation (1) ·
Visualisation (1)
Alternative splicing (1) ·
CLIP-Seq (1) ·
Cancer biology (1) ·
ChIP-seq (2) ·
Community analysis (2) ·
Copy number estimation (1) ·
DNA methylation (4) ·
Epigenetics (3) ·
Epigenomics (2) ·
Exome analysis (1) ·
Exome capture (2) ·
Gene expression analysis (1) ·
Gene regulation (1) ·
Gene structure (1) ·
Genomics (8) ·
Genotyping (1) ·
HITS-CLIP (1) ·
ICLIP (1) ·
Indel detection (1) ·
Mapping (4) ·
Metabolic reconstruction (1) ·
Metagenomics (8) ·
Next Generation Sequencing (1) ·
PAR-CLIP (1) ·
Phylogenetics (4) ·
RNA-Seq (3) ·
RNA-Seq alignment (1) ·
RNA-Seq quantification (3) ·
Rarefaction (1) ·
Read alignment (1) ·
Resequencing (1) ·
SNP detection (2) ·
Sequence analysis (3) ·
Sequence assembly (de novo assembly) (2) ·
Sequencing (7) ·
Structural variation (2) ·
Transcriptomics (4) ·
Whole genome resequencing (1)
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