Browse data: Bioinformatics application
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Bioinformatics method:
Ab-initio gene prediction (1) ·
Adapter removal (1) ·
Annotation (3) ·
Base-calling (1) ·
Bisulfite mapping (1) ·
Collapsing methods (1) ·
DNA barcoding (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 (3) ·
RNA-Seq analysis (1) ·
RRNA filtering (1) ·
Read mapping (6) ·
Read pre-processing (2) ·
SNP calling (2) ·
Sequence alignment (6) ·
Sequence alignment visualisation (2) ·
Sequence analysis (4) ·
Sequence assembly (7) ·
Sequence assembly (de-novo assembly) (2) ·
Sequence assembly validation (2) ·
Sequence assembly visualisation (1) ·
Sequence contamination filtering (4) ·
Sequence error correction (1) ·
Sequence motif discovery (1) ·
Sequence parsing (1) ·
Sequence trimming (3) ·
Sequencing quality control (1) ·
Statistical calculation (1) ·
Variant calling (2) ·
Variant classification (1) ·
Visualisation (5)
Biological domain:
Alternative splicing (1) ·
ChIP-seq (1) ·
Community analysis (2) ·
Copy number estimation (1) ·
Data handling (1) ·
Epigenomics (2) ·
Exome analysis (1) ·
Exome and whole genome variant detection (1) ·
Genetic variation (1) ·
Genetics (1) ·
Genomics (13) ·
Indel detection (2) ·
Mapping (2) ·
Metagenomics (9) ·
Next Generation Sequencing (1) ·
Personalised medicine (1) ·
Phylogenetics (6) ·
Population genetics (1) ·
Protein structure analysis (1) ·
Quality control (1) ·
RNA-Seq (2) ·
RNA-Seq alignment (2) ·
Rarefaction (1) ·
Read binning (1) ·
Regulatory RNA (1) ·
Resequencing (1) ·
SNP detection (5) ·
Sequence alignment (2) ·
Sequence analysis (6) ·
Sequence assembly (de novo assembly) (6) ·
Sequencing (4) ·
Structural variation (2) ·
Transcriptomics (6) ·
Whole genome resequencing (4)
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