12885_2019_5494_MOESM5_ESM.xlsx (32.9 kB)
Additional file 5: of Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families
dataset
posted on 2019-04-04, 05:00 authored by Rajendra Shahi, Sylvia De Brakeleer, Ben Caljon, Ingrid Pauwels, Maryse Bonduelle, Sofie Joris, Christel Fontaine, Marian Vanhoeij, Sonia Van Dooren, Erik Teugels, Jacques De GrèveTypes and number of variants detected (exome- and CAGP-wide) before and after variant filtration in each BC patient and control. (XLSX 32 kb)