ea0098b22 | Basic Science | NANETS2023
Sukrithan Vineeth
, Boateng Isaiah
, Liyanarachchi Sandya
, Jain Prachi
, Buss Jill
, Parwani Anil
, Shah Manisha H.
, Das Komal
, Yearsely Martha
, Konda Bhavana
, Brock Pamela
, Eisfeld Ann-Kathrin
Background: We conducted whole-exome sequencing (WES) of germline(g) and somatic(s) DNA from a prospective cohort of patients with NENs (n =151) to study the genetic predisposition to NENs.Methods: Variants obtained from gWES were filtered using a standard bio-informatics pipeline. Variant Effect Predictor (Release 107) was applied to obtain population allele frequencies. Variants were restricted to those among 974 genes obtained by combining pu...