Browse data: Bioinformatics application
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Bioinformatics application > Language :
C++ or
Fortran F77
& Operating system :
Cross-Platform or
Linux
& Technology:
Illumina
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Subcategory: Missing email (29)
Ab-initio gene prediction (1) ·
Adapter removal (2) ·
Annotation (1) ·
Bisulfite mapping (3) ·
Comparative genomics (1) ·
Correlation (1) ·
DNA barcoding (1) ·
Expectation Maximisation (1) ·
File reformatting (1) ·
Gene expression analysis (1) ·
Genome indexing (Burrows-Wheeler) (1) ·
Graph reduction (1) ·
Heat map generation (1) ·
K-mer counting (1) ·
Learning algorithm (1) ·
Local sequence alignment (1) ·
Localised reassembly (1) ·
Mapping (1) ·
Peak calling (1) ·
Quality control (1) ·
Read mapping (16) ·
Read pre-processing (1) ·
SNP calling (2) ·
Scaffolding (1) ·
Sequence alignment (10) ·
Sequence analysis (1) ·
Sequence assembly (10) ·
Sequence assembly (de-novo assembly) (2) ·
Sequence assembly validation (1) ·
Sequence clustering (1) ·
Sequence error correction (2) ·
Sequence parsing (1) ·
Sequence trimming (1) ·
Split-read mapping (1) ·
Statistical calculation (1) ·
Transcriptome assembly (1) ·
Variant calling (1) ·
Visualisation (1)
Alternative splicing (3) ·
ChIP-seq (4) ·
DNA-Seq (1) ·
DNA methylation (2) ·
De-novo assembly (1) ·
Epigenetics (2) ·
Exome and whole genome variant detection (1) ·
Gene expression analysis (1) ·
Gene structure (1) ·
Genomic assembly (1) ·
Genomics (10) ·
Indel detection (3) ·
Mapping (3) ·
Metagenomics (2) ·
Next Generation Sequencing (1) ·
Phylogenetics (1) ·
Protein structure analysis (1) ·
Quality control (1) ·
RNA-Seq (7) ·
RNA-Seq alignment (4) ·
RNA-Seq quantification (3) ·
Regulatory RNA (1) ·
SNP detection (7) ·
Sequence alignment (1) ·
Sequence analysis (4) ·
Sequence assembly (1) ·
Sequence assembly (de-novo assembly) (1) ·
Sequence assembly (de novo assembly) (6) ·
Sequencing (2) ·
Statistical calculation (1) ·
Structural variation (1) ·
Transcriptomics (5) ·
Whole genome resequencing (3)
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