Browse data: Bioinformatics application
Choose a category:
Bioinformatics application > Operating system :
Solaris or
Windows or
any
& Technology :
Sanger or
all
Click on one or more items below to narrow your results.
Subcategory: Missing email (19)
C (3) ·
C++ (8) ·
Fortran (1) ·
Java (8) ·
Java 7 (1) ·
Perl (3) ·
Pilot Script (1) ·
R (1) ·
Tcl (1)
Ab-initio gene prediction (1) ·
Adapter removal (1) ·
Annotation (4) ·
Base-calling (2) ·
Bisulfite mapping (1) ·
Chromatogram visualisation (1) ·
Collapsing methods (1) ·
Comparative genomics (1) ·
DNA barcoding (1) ·
File reformatting (1) ·
Gene expression analysis (1) ·
Genome visualisation (2) ·
Heat map generation (1) ·
Local sequence alignment (1) ·
Mapping (1) ·
Modelling and simulation (1) ·
RNA-Seq analysis (1) ·
Read mapping (7) ·
Read pre-processing (1) ·
SNP calling (2) ·
Sequence alignment (7) ·
Sequence alignment visualisation (3) ·
Sequence analysis (3) ·
Sequence assembly (9) ·
Sequence assembly (de-novo assembly) (1) ·
Sequence assembly editing (1) ·
Sequence assembly validation (2) ·
Sequence assembly visualisation (2) ·
Sequence contamination filtering (3) ·
Sequence error correction (1) ·
Sequence motif discovery (1) ·
Sequence parsing (1) ·
Sequence trimming (3) ·
Sequencing quality control (1) ·
Statistical calculation (1) ·
Variant calling (4) ·
Variant classification (1) ·
Visualisation (6)
Alternative splicing (1) ·
ChIP-seq (2) ·
Comparative genomics (2) ·
Copy number estimation (1) ·
Data handling (1) ·
Epigenomics (2) ·
Exome analysis (1) ·
Exome and whole genome variant detection (1) ·
Gene expression analysis (1) ·
Genetic variation (1) ·
Genetics (1) ·
Genomics (14) ·
Genotyping (1) ·
Indel detection (2) ·
Mapping (2) ·
Metagenomics (5) ·
Microbial Surveillance (1) ·
Next Generation Sequencing (2) ·
Personalised medicine (1) ·
Phylogenetics (4) ·
Population genetics (1) ·
Protein structure analysis (1) ·
Quality control (1) ·
RNA-Seq (3) ·
RNA-Seq alignment (1) ·
Read binning (1) ·
Regulatory RNA (1) ·
Resequencing (1) ·
SNP detection (6) ·
Sequence alignment (2) ·
Sequence analysis (6) ·
Sequence assembly (de novo assembly) (5) ·
Sequencing (3) ·
Structural variation (3) ·
Transcriptomics (4) ·
Whole genome resequencing (5)
Showing below up to 25 results in range #1 to #25.
View (previous 250 | next 250) (20 | 50 | 100 | 250 | 500)
B
C
D
G
G cont.
M
P
R
S