Browse data: Bioinformatics application
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Bioinformatics application > Operating system :
Linux CentOS 6.5 or
Mac OS X
& Technology :
Any sequencing platform or
Anything that can be assembled with Celera or Newbler or
Pacific Biosciences or
Pyrosequencing (QIAGEN) or
Sanger
Click on one or more items below to narrow your results.
Subcategory: Missing email (21)
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 (7) ·
Read pre-processing (2) ·
SNP calling (2) ·
Sequence alignment (7) ·
Sequence alignment visualisation (2) ·
Sequence analysis (4) ·
Sequence assembly (8) ·
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)
Alternative splicing (1) ·
ChIP-seq (2) ·
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 (14) ·
Indel detection (3) ·
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 (3) ·
Rarefaction (1) ·
Read binning (1) ·
Regulatory RNA (1) ·
Resequencing (1) ·
SNP detection (6) ·
Sequence alignment (2) ·
Sequence analysis (6) ·
Sequence assembly (de-novo assembly) (1) ·
Sequence assembly (de novo assembly) (7) ·
Sequencing (4) ·
Structural variation (2) ·
Transcriptome assembly (1) ·
Transcriptomics (6) ·
Whole genome resequencing (5)
Showing below up to 26 results in range #1 to #26.
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