Please select the pipeline for your desired project(s).
WGTS Pipeline (snvs/indels, copy number, structural variants, expression data and gene fusions)
For each case, this requires sequence data from Whole Genome libraries (tumour + matched normal), and Whole Transcriptome (tumour only)
WGS or WES Somatic Calling Pipeline (somatic snvs and copy number, structural variants only from WG libraries)
For each cases, this requires sequence data from Whole Genome or Whole Exome libraries (tumour + matched normal)
WGS or WES Tumour only (snvs and indels)
Requires sequence data generated from tumour libraries
WTS Pipeline (expression + fusions)
Requires sequence data from Whole transcriptome libraries
WGS or WES Germline Pipeline (snvs and indels)Requires sequence data from WGS or WES libraries