Browse data: Bioinformatics application
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Subcategory: Missing email (13)
*NIX (1) ·
10.8 (1) ·
Linux (6) ·
Linux 64 (1) ·
Linux CentOS 6.5 (1) ·
Linux Ubuntu 12.04 (1) ·
Mac OS X (7) ·
Mac OS X 10.7 (1) ·
Mac OS X; x86 64 (1) ·
UNIX (6) ·
Unix (1) ·
Unix-like (1) ·
Windows (7) ·
Windows 7 64-bit or Higher (1) ·
Windows 7 or Higher (1) ·
all supporting JVM (1) ·
or 10.9 (1)
Ab-initio gene prediction (1) ·
Analysis (1) ·
Annotation (2) ·
Biological interpretation (1) ·
Classification (1) ·
Comparative genomics (1) ·
Differential expression analysis (1) ·
File reformatting (1) ·
Genome visualisation (1) ·
Graph reduction (1) ·
K-mer counting (1) ·
Learning algorithm (1) ·
Local sequence alignment (1) ·
Nucleic acid sequence feature detection (1) ·
Peak calling (2) ·
Peptide mass fingerprint (1) ·
Quality control (1) ·
RNA-Seq analysis (1) ·
RRNA filtering (1) ·
Read mapping (5) ·
Read pre-processing (2) ·
Sequence alignment (5) ·
Sequence analysis (1) ·
Sequence assembly (6) ·
Sequence contamination filtering (3) ·
Sequence error correction (1) ·
Sequence trimming (3) ·
Sequencing quality control (1) ·
Variant calling (2) ·
Visualisation (1) ·
Workflows (1)
Alternative splicing (2) ·
ChIP-seq (3) ·
Comparative genomics (2) ·
DNA-Seq (1) ·
Data handling (1) ·
Epidemiology (1) ·
Epigenomics (1) ·
Genomics (5) ·
Genotyping (1) ·
Indel detection (1) ·
MeDIP-Seq (1) ·
Metabolic reconstruction (1) ·
Metagenomics (6) ·
Methyl-Seq (1) ·
Microbial Surveillance (3) ·
Pathway or network analysis (1) ·
Phylogenetics (4) ·
Public health and epidemiology (1) ·
Quality control (2) ·
RNA (1) ·
RNA-Seq (3) ·
RNA-Seq alignment (3) ·
RNA-Seq quantification (1) ·
Read binning (1) ·
Regulatory genomics (1) ·
Resequencing (1) ·
SNP detection (3) ·
Sequence alignment (1) ·
Sequence analysis (1) ·
Sequence assembly (3) ·
Sequence assembly (de-novo assembly) (1) ·
Sequence assembly (de novo assembly) (2) ·
Sequencing (1) ·
Small RNA-Seq (1) ·
Transcription factors and regulatory sites (1) ·
Transcriptome assembly (1) ·
Transcriptomics (6) ·
Whole genome resequencing (3) ·
Workflows (1)
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