Widely used in studies on:

  • * Human Genomics
  • * Cancer

 

Lab protocols we can do:

  • * Exome sequencing
  • * Whole genome sequencing
  • * Gene panel sequencing
  • * Low input DNA sequencing (FFPE)
 
 
Bioinformatics analysis of:
 
  • * Somatic variant identification (SNVs, Indels, CNVs)
  • * Cancer cell fraction
  • * Mutational signatures/burden
  • * Cancer-Connect Genome Phenome Analysis Platform (in development)
 
 

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