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).
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