Browse data: Bioinformatics application
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Subcategory: Missing email (43)
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Bioinformatics method:
Adapter removal (2) ·
Assembly (1) ·
Base-calling (1) ·
Bisulfite mapping (2) ·
Conversion (1) ·
DNA barcoding (2) ·
De-novo assembly (1) ·
Differential Binding (1) ·
Haplotype inference (1) ·
Hidden Markov Model (1) ·
Local sequence alignment (1) ·
Mapping (3) ·
Modelling and simulation (3) ·
Nucleic acid sequence feature detection (1) ·
Peak calling (2) ·
Quality control (1) ·
RRNA filtering (1) ·
Read alignment (1) ·
Read mapping (17) ·
Read pre-processing (5) ·
Read summarisation (1) ·
Sequence alignment (6) ·
Sequence analysis (2) ·
Sequence annotation (1) ·
Sequence assembly (5) ·
Sequence contamination filtering (3) ·
Sequence error correction (1) ·
Sequence parsing (1) ·
Sequence redundancy removal (1) ·
Sequence trimming (5) ·
Sequencing quality control (5) ·
Split-read mapping (1) ·
Standardisation and normalisation (1) ·
Statistical calculation (2) ·
Visualisation (1) ·
Whole genome breakend assembly (1)
Biological domain:
Cancer biology (2) ·
ChIP-seq (3) ·
Community analysis (2) ·
Copy number estimation (3) ·
DNA methylation (4) ·
Epigenetics (3) ·
Epigenomics (4) ·
Exome (1) ·
Exome analysis (2) ·
Exome and whole genome variant detection (1) ·
Exome capture (1) ·
Gene structure (2) ·
Genetic variation analysis (1) ·
Genomics (17) ·
High-throughput sequencing (1) ·
Indel detection (2) ·
Mapping (6) ·
Metagenomics (6) ·
Next Generation Sequencing (4) ·
Personalised medicine (1) ·
Phylogenetics (3) ·
Protein structure analysis (1) ·
RNA-Seq (2) ·
RNA-Seq alignment (2) ·
Rarefaction (1) ·
Regulatory genomics (1) ·
Resequencing (1) ·
SNP detection (2) ·
Sequence alignment (1) ·
Sequence analysis (4) ·
Sequence assembly (1) ·
Sequence assembly (de-novo assembly) (1) ·
Sequence assembly (de novo assembly) (2) ·
Sequencing (7) ·
Structural variation (3) ·
Transcription factors and regulatory sites (1) ·
Transcriptome assembly (1) ·
Transcriptomics (6) ·
Whole genome resequencing (2)
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