Diagnosis of copy number variation by Illumina next generation sequencing is comparable in performance to oligonucleotide array comparative genomic hybridisation

Autor: Hayes, J.L., Tzika, A., Thygesen, H., Berri, S., Wood, H.M., Hewitt, S., Pendlebury, M., Coates, A., Willoughby, L., Watson, C.M., Rabbitts, P., Roberts, P., Taylor, G.R.
Zdroj: In Genomics September 2013 102(3):174-181
Databáze: ScienceDirect