Targeted panel sequencing data from PanNEN samples. Sample ID is annotated in the following manner: each patient is given a number and "P" is appended to the patient number if it is a primary tumor, "
The goal of this study was to obtain the complete genome sequence of the C57L/J in order to compare it to the C57BL/6J and identify variants that we could use for genetic mapping between the two strai
We propose in this paper a set-valued (SV) system model, which is a generalized form of logistic (LG) and Probit (Probit) regression, to be considered as a method for discovering genetic variants, esp
