Browse data: Bioinformatics application
Choose a category:
Bioinformatics application > Operating system
:
Linux CentOS 6.5
or
all supporting JVM
or
any
or
platform-independent ![](/w/extensions/SemanticDrilldown/skins/filter-x.png)
![](/w/extensions/SemanticDrilldown/skins/filter-x.png)
![](/w/extensions/SemanticDrilldown/skins/filter-x.png)
![](/w/extensions/SemanticDrilldown/skins/filter-x.png)
![](/w/extensions/SemanticDrilldown/skins/filter-x.png)
![](/w/extensions/SemanticDrilldown/skins/filter-x.png)
Click on one or more items below to narrow your results.
Subcategory: Missing email (17)
Bash (2) ·
C (2) ·
C++ (2) ·
Java (12) ·
Java 7 (1) ·
JavaScript (2) ·
Perl (3) ·
Python (4) ·
R (2)
Data retrieval (2) ·
Differential expression analysis (3) ·
File reformatting (1) ·
Filtering (1) ·
Format conversion (1) ·
Functional analysis (1) ·
Functional enrichment (1) ·
Genome visualisation (3) ·
Genomic region matching (1) ·
Genotyping (1) ·
Methylation analysis (1) ·
Pathway or network analysis (1) ·
Peak calling (4) ·
Plotting and rendering (1) ·
RNA-Seq analysis (1) ·
Read mapping (7) ·
SNP calling (1) ·
Sequence alignment (3) ·
Sequence alignment analysis (1) ·
Sequence alignment visualisation (2) ·
Sequence assembly (2) ·
Sequence assembly validation (1) ·
Sequence contamination filtering (2) ·
Sequence error correction (1) ·
Sequence motif comparison (1) ·
Sequence motif discovery (2) ·
Sequence motif recognition (2) ·
Sequence trimming (3) ·
Sequencing quality control (2) ·
Statistical calculation (1) ·
Variant calling (1) ·
Viewer (1) ·
Visualisation (5) ·
Workflows (1)
Alternative splicing (1) ·
Biomedical Sciences (1) ·
ChIP-seq (6) ·
Comparative genomics (1) ·
Copy number estimation (1) ·
DNA methylation (1) ·
Exome capture (1) ·
Gene regulation (2) ·
Genetic variation (1) ·
Genomics (9) ·
Immunoprecipitation experiment (1) ·
Indel detection (1) ·
Metagenomics (2) ·
Phylogenetics (1) ·
Quality control (2) ·
RNA (1) ·
RNA-Seq (2) ·
RNA-Seq alignment (2) ·
RNA-Seq quantification (1) ·
Read binning (1) ·
Resequencing (1) ·
SNP detection (2) ·
Sequence alignment (1) ·
Sequence analysis (2) ·
Sequence assembly (de-novo assembly) (1) ·
Sequence assembly (de novo assembly) (3) ·
Sequence motifs (2) ·
Sequencing (1) ·
Structural variation (1) ·
Transcription factors and regulatory sites (2) ·
Transcriptome assembly (1) ·
Transcriptomics (2) ·
Whole genome resequencing (2) ·
Workflows (1)
Showing below up to 22 results in range #1 to #22.
View (previous 250 | next 250) (20 | 50 | 100 | 250 | 500)