Browse data: Bioinformatics application
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Bioinformatics application > Language :
C or
C++ or
CUDA or
Fortran F77
& Licence :
C++ or
GPL or
GPLv3
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Subcategory: Missing email (50)
*NIX (1) ·
Linux (27) ·
Linux 64 (7) ·
Mac OS X (21) ·
Mac OS X; x86 64 (1) ·
POSIX (2) ·
Solaris (2) ·
UNIX (14) ·
Unix (1) ·
Windows (8) ·
any (1)
Adapter removal (2) ·
Base-calling (1) ·
Bisulfite mapping (3) ·
DNA barcoding (2) ·
Enrichment (1) ·
Expectation Maximisation (1) ·
Genome indexing (1) ·
Graph reduction (1) ·
K-mer counting (3) ·
Learning algorithm (1) ·
Local sequence alignment (2) ·
Localised reassembly (1) ·
Mapping (2) ·
Modelling and simulation (1) ·
Peak calling (2) ·
Quality assessement (1) ·
Quality control (1) ·
RRNA filtering (1) ·
Read mapping (23) ·
Read pre-processing (3) ·
Read summarisation (2) ·
SNP annotation (1) ·
Sequence alignment (10) ·
Sequence alignment comparison (1) ·
Sequence analysis (1) ·
Sequence assembly (6) ·
Sequence assembly validation (1) ·
Sequence contamination filtering (3) ·
Sequence error correction (2) ·
Sequence motif comparison (1) ·
Sequence motif discovery (1) ·
Sequence parsing (1) ·
Sequence redundancy removal (1) ·
Sequence trimming (2) ·
Sequencing quality control (3) ·
Signal (1) ·
Statistical calculation (2) ·
Variant calling (2) ·
Visualisation (1)
Alternative splicing (1) ·
ChIP-seq (2) ·
Comparative genomics (1) ·
Copy number estimation (1) ·
DNA methylation (3) ·
Epigenetics (1) ·
Exome and whole genome variant detection (2) ·
Functional genomics (1) ·
Gene expression analysis (1) ·
Genomics (18) ·
Indel detection (5) ·
Mapping (5) ·
Metagenomics (4) ·
Next Generation Sequencing (4) ·
Phylogenetics (1) ·
Protein structure analysis (1) ·
RNA-Seq (3) ·
RNA-Seq alignment (4) ·
RNA-Seq quantification (1) ·
SNP (1) ·
SNP detection (7) ·
Sequence alignment (1) ·
Sequence analysis (2) ·
Sequence assembly (de-novo assembly) (1) ·
Sequence assembly (de novo assembly) (4) ·
Sequence motifs (1) ·
Sequencing (4) ·
Storage (1) ·
Structural variation (2) ·
Transcriptome assembly (1) ·
Transcriptomics (5) ·
Whole genome resequencing (3)
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