Identification of genetic diseases
To detect and characterize viruses, bacteria, and other microbes and diagnose infectious diseases
Pharmacogenomics to determine how individuals react to drugs and use this knowledge to choose and or design the safest and most effective treatment for the individual
Cancer genomics - WGS and WES helps identify genetic mutations such as BCR-ABL important for cancer diagnosis, grouping of tumors into subtypes, and tretament optimization.
Genomic surveillance - WGS and WES help identify new or existing genetic variants in viruses and other microbes and this is useful in the analysis, vigilance and control of pathogens such as SARS CoV2
Microbial genetics - WGS and WES are used to study microbes for purposes of disease control, gene cloning, research, determintion of bacterial drug resistance, and for production of products like antibiotics and harmones.
PhD-level bioinformatics analysis is bundled with the sequencing services and aids in the accurate identification of the following:
long read sequencing resolves structural variants, repeat regions and phasing with long reads.
Direct RNA sequencing eliminates bias, allowing for a comprehensive assessment of epigenetic modifications
Pathogens can be detected accurately and strains typed precisely.
Results are available in 10 working days.
Client information is held in struct confidence and all data is returned to the client or discrded unlesss the client asks us to store it.
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