The Genotyping, Index Sequence Capture (ISC) & Single-cell Sequencing team within DNA Pipelines Operations is a high throughput Illumina® library creation team specialising in producing libraries quickly and at scale from extracted material and single cells. Once each type of library prep is complete the samples are sent to be sequenced on the Wellcome Sanger Institute’s collection of Illumina® instruments including the NovaSeq 6000, HiSeq X, Hiseq 4000, Hiseq 2500 and MiSeq.
The library preparation services provided by our group include:
• Index Sequence capture (ISC)
• Single cell RNA (scRNA)
• Genotyping by Sequencing (GbS)