Bioinformatics services

Table of contents:

• CHIP-Seq
• miRNA/small RNA
• Digital Gene Expression (RNASeq)
• DNA Methylation studies
• Bacterial genome sequencing and basic annotation
• Whole Genome Resequencing
• Variation detection

Novocraft Technologies offers an extensive list of customized analysis services that cover a broad range of applications supported by next-generation sequencing technologies such as:

• CHIP-Seq
• miRNA/small RNA
• Digital Gene Expression (RNASeq)
• DNA Methylation studies
• Whole genome Resequencing
• Automated genome annotation
  • Genome assembly
  • Reference-guided
• De novo
• Variation detection
  • SNP/mutation identification
  • Structural variation detection

These services utilize in-house technologies e.g. Novoalign as well as a combination of standard open bioinformatics software. In such cases all raw data, analysis result files and a summary reports are delivered to clients to facilitate their work or future publications.

Our offerings are sequencing platform independent and we provide a free quoting service depending on budget, delivery requirements and the amount of data that needs to be processed. In addition to these bioinformatics services, we work with sequencing vendors to provide cost-effective rates to customers who require an end-to-end solution.

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