Bioinformatics
The Bioinformaticians in the team have expertise in handling NGS sequencing data and analysis and interpretation. Their expertise is in creating pipelines for processing raw data and interpretation. This includes:
- Whole genome sequencing analysis of leukaemia, lymphomas and solid tumours
- Tailored pipelines for ctDNA analysis:
- error corrected sequencing,
- comprehensive WGS, panel, germline, tumour, tumour normal subtractions
- Pipeline for SNVs, copy number, abnormality, structural variants, genomic complexity detection
- Dedicated methods for ctDNA analysis that incorporate error correction and increased sensitivity on liquid biopsies
- Cloud-based platforms to share raw data and secondary files, BAMS, VCF as required
- Assistance with variant interpretation
- Reporting to clinical grade standard and specified turn-around times at additional cost.