The force−extension relation for a semiflexible polymer confined in a nanoslit is investigated. Both the effective correlation length and force−extension relation change as the chain goes from 3D (large slit heights) to 2D (tight confinement). At low forces, correlations along the polymer give an effective dimensionality. The strong force limit can be interpolated with the weak force limit for two regimes: when confinement dominates over extensile force and vice versa. These interpolations give good agreement with simulations for all slit heights and forces. We thus generalize the Marko-Siggia force− extension relation for DNA and other semiflexible biopolymers in nanoconfinement.M any recent studies have focused on static 1−9 and dynamic 10−15 properties of semiflexible biopolymers, such as DNA, within nanoslits, 16,17 nanochannels, 18−21 and crowded environments. 22−24 Here, we study polymers of contour length L C confined within nanoslits and subjected to a stretching force F with resulting extension x. We seek to generalize the Marko-Siggia (MS) force−extension relation (FER) to confined environments. Experimental examples include DNA stretched by electric fields in nanoslits 25 and tug-of-war or nanopit-type devices. 26−29 Both the 3D 30,31 and the 2D 32 limits of the FER have been studied extensively, but few studies investigate the crossover from 3D to 2D with confinement. 33 While scaling theories quite successfully predict conformations and dynamics of confined macromolecules, 34