Genomics approaches such as whole genome sequencing (WGS), whole exomes sequencing (WES) or targeted re-sequencing allow for the identification of genetic variation ranging from single nucleotide polymorphisms (SNP) over small insertions and deletions (indels) to large sequence rearrangements.
Identification of genetic variation allows high-throughput genotyping and facilitates population studies such as genome-wide association studies (GWAS).

We are happy to support you amongst other analyses with:

  • whole genome sequencing (WGS) analysis
  • targeted genome sequencing analysis
  • genome assembly
  • whole exome sequencing (WES) analysis
  • variant calling
  • genotyping
  • sequence annotation
  • association studies (e.g. GWAS)

Please contact us to for an initial consultation to discuss how we can support you to solve your specific challenge.

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