Browse data: Bioinformatics application
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Bioinformatics application > Operating system :
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Subcategory: Missing email (38)
Bourne shell (1) ·
C (11) ·
C# (1) ·
C++ (13) ·
Java (12) ·
JavaScript (1) ·
PHP (1) ·
Perl (5) ·
Python (5) ·
R (3)
Adapter removal (2) ·
Annotation (1) ·
Base-calling (2) ·
Bisulfite mapping (2) ·
File reformatting (2) ·
Gene expression profiling (1) ·
Genome indexing (Burrows-Wheeler) (1) ·
Genome visualisation (1) ·
Mapping (2) ·
MicroRNA detection (2) ·
Phase pattern prediction (1) ·
Quality assessement (1) ·
Read mapping (17) ·
Read pre-processing (2) ·
Read summarisation (2) ·
SNP calling (1) ·
Sequence alignment (6) ·
Sequence analysis (1) ·
Sequence annotation (1) ·
Sequence assembly (8) ·
Sequence contamination filtering (1) ·
Sequence error correction (1) ·
Sequence trimming (1) ·
Split-read mapping (1) ·
Variant calling (1) ·
Visualisation (1)
Alternative splicing (1) ·
Cancer biology (1) ·
ChIP-seq (2) ·
Clone verification (1) ·
Comparative genomics (2) ·
Copy number estimation (2) ·
DNA methylation (2) ·
DNA transcription (1) ·
Epigenomics (1) ·
Exome (1) ·
Exome analysis (1) ·
Exome and whole genome variant detection (1) ·
Exome capture (1) ·
Gene structure (3) ·
Genetic variation (1) ·
Genomics (12) ·
Indel detection (5) ·
Mapping (2) ·
Metagenomics (2) ·
Microbial Surveillance (1) ·
Next Generation Sequencing (3) ·
Personalised medicine (1) ·
Phylogenetics (1) ·
RNA-Seq (4) ·
RNA-Seq alignment (5) ·
RNA-Seq quantification (1) ·
Regulatory RNA (1) ·
Resequencing (1) ·
SNP detection (5) ·
Sequence analysis (2) ·
Sequence assembly (1) ·
Sequence assembly (de-novo assembly) (1) ·
Sequence assembly (de novo assembly) (3) ·
Sequencing (8) ·
Small RNA Sequencing (1) ·
Transcriptome assembly (1) ·
Transcriptomics (3) ·
Whole genome resequencing (4) ·
Workflows (7)
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- SCALCE
- SeqMan NGen
- SeqSphere+
- Sequedex
- SequenceVariantAnalyzer
- SiLoCo
- Skewer
- SOAPfusion
- SsahaSNP
- Subread
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