Bioinformatics solutions
Sequencing data
We process data from all current next-generation sequencing platforms as well as traditional Sanger sequence data. Generally, data processing involves the removal of adaptor sequences and quality clipping. All subsequent analyses depend on the application and type of data.
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Roche 454 sequencer |
ABI SOLID sequencer |
Illumina Solexa sequencer |
Genomics / Genotyping
- Sequence variation detection / Resequencing applications
- de novo assembly
- Copy number alterations
- Genome rearrangement studies
Transcriptomics
- Transcriptome assembly
- small RNA analyses
- Splice variant discovery
ChIP-Seq
- Protein / DNA binding
- Protein / RNA binding
Metagenomic / Population studies
- Species enumeration
Mass spectrometry data
Proteomics
Metabolomics
Functional annotation / Sequence analysis
Genome annotation
Motif discovery
Regulatory module detection
Network / System level analysis
Whole Genome Evolution