S-F Chin, A Santonja, M Grzelak, S Ahn, S-J Sammut, H Clifford, OM Rueda, M Pugh, MA Goldgraben, HA Bardwell, EY Cho, E Provenzano, F Rojo, E Alba, C Caldas
Journal name: 
Exp Mol Pathol
Citation info: 
Pathology archives with linked clinical data are an invaluable resource for translational research, with the limitation that most cancer samples are formalin-fixed paraffin-embedded (FFPE) tissues. Therefore, FFPE tissues are an important resource for genomic profiling studies but are under-utilised due to the low amount and quality of extracted nucleic acids. We profiled the copy number landscape of 356 breast cancer patients using DNA extracted FFPE tissues by shallow whole genome sequencing. We generated a total of 491 sequencing libraries from 2 kits and obtained data from 98.4% of libraries with 86.4% being of good quality. We generated libraries from as low as 3.8 ng of input DNA and found that the success was independent of input DNA amount and quality, processing site and age of the fixed tissues. Since copy number alterations (CNA) play a major role in breast cancer, it is imperative that we are able to use FFPE archives and we have shown in this study that sWGS is a robust method to do such profiling.
Research group: 
Caldas Group
E-pub date: 
01 Jun 2018
Users with this publication listed: 
Carlos Caldas
Mae Goldgraben
Marta Grzelak
Oscar Rueda
Stephen-John Sammut
Suet-Feung Chin