Sarcoma and the 100,000 Genomes Project: our experience and changes to practice

• المؤلفون الرئيسيون: Sophie C Prendergast (مؤلف), Anna‐Christina Strobl (مؤلف), William Cross (مؤلف), Nischalan Pillay (مؤلف), Sandra J Strauss (مؤلف), Hongtao Ye (مؤلف), Daniel Lindsay (مؤلف), Roberto Tirabosco (مؤلف), Jane Chalker (مؤلف), Shazia S Mahamdallie (مؤلف), Alona Sosinsky (مؤلف), RNOH Pathology Laboratory and Biobank Team (مؤلف), Genomics England Research Consortium (مؤلف), Adrienne M Flanagan (مؤلف), Fernanda Amary (مؤلف)
• التنسيق: كتاب
• منشور في: Wiley, 2020-10-01T00:00:00Z.
• الموضوعات: article
• الوصول للمادة أونلاين: Connect to this object online.

Abstract The largest whole genome sequencing (WGS) endeavour involving cancer and rare diseases was initiated in the UK in 2015 and ran for 5 years. Despite its rarity, sarcoma ranked third overall among the number of patients' samples sent for sequencing. Herein, we recount the lessons learned...