Genetic alterations play a key role in the initiation of a range of diseases. For instance, in cancer there are tumor clones with distinct genetic alterations, such as single nucleotide variations (SNVs), copy number variations (CNVs) and indels. This heterogeneity is vital to tumor development, proliferation and metastatic potential, while also playing a key role in therapy resistance. Single-cell sequencing is used to investigate the (epi)genome of single cells and to unravel the concept of heterogeneity.
In recent years, many novel sequencing technologies have been developed in the research groups of Alexander van Oudenaarden and Geert Kops. To make these techniques widely available, Single-Cell Core was launched in 2020. Located at the Hubrecht Institute, we have had early access to technologies that no other labs have been running yet. This allowed us to develop a unique expertise on services involving chromatin profiling and karyotyping, giving us a head start in the field of single-cell DNA sequencing. Since then, Single-Cell Core has expanded its client portfolio from research institutes at the Utrecht Science Park, to medical centers in the Netherlands and to science organizations abroad.
Technologies that we currently offer include single-cell chromatin immunocleavage sequencing (scChIC-seq), single-cell transcriptome + chromatin immunocleavage sequencing (scTChIC-seq), single-cell karyotype sequencing (scKaryo-seq) and single-cell EdU-sequencing (scEdU-seq).