Investigation of a global mouse methylome atlas reveals subtype-specific copy number alterations in pediatric cancer models.

Despite this clear overlap, statistical analysis indicated that the synteny between mouse chromosome 4 loss and the human summary plots was either not significant (ALK-driven pHGG) or barely significant (NTRK2-driven pHGG; P = 0.02), as a result of the small human patient population harboring chromosomal aberrations.

also in 875 other papers

3e,f ), and these predicted matches were found to be highly significant (Extended Data Fig. 5b and Supplementary Tables 4 – 6 ).

also in 132,142 other papers