config
Registry-driven config models for DCE selection points.
Each DCE selection point — pharmacokinetic model, T1 mapping method,
signal-to-concentration model, and population AIF — declares its tunable
knobs as a :class:~osipy.common.config.MethodConfig. These compose into
discriminated unions for the CLI config (so selecting a method surfaces
exactly that method's parameters and rejects cross-method keys), and the
matching *_REGISTRY maps build the live component from a validated
config instance via :func:~osipy.common.config.construct_from_config.
Mirrors :mod:osipy.dsc.deconvolution.config. Adding @register_model
(or @register_t1_method / @register_concentration_model /
@register_aif) plus an entry here automatically surfaces the new option
(and its knobs) as a CLI toggle that both validates input and builds the
component — an option can never be "collected but silently ignored".
References
.. [1] OSIPI CAPLEX, https://osipi.github.io/OSIPI_CAPLEX/ .. [2] Dickie BR et al. MRM 2024;91(5):1761-1773. doi:10.1002/mrm.29840
Bases: MethodConfig
Standard Tofts model (OSIPI: M.IC1.004).
Bases: MethodConfig
Extended Tofts model with plasma term (OSIPI: M.IC1.005).
Bases: MethodConfig
Patlak model (OSIPI: M.IC1.006).
Bases: MethodConfig
Two-compartment exchange model (OSIPI: M.IC1.009).
Bases: MethodConfig
Two-compartment uptake model (2CUM).
Bases: MethodConfig
Variable Flip Angle T1 mapping (OSIPI: P.NR2.002).
Bases: MethodConfig
Look-Locker inversion-recovery T1 mapping (OSIPI: P.NR2.004).
Bases: MethodConfig
Spoiled gradient-echo signal-to-concentration model (OSIPI: P.SC1.001).
Bases: MethodConfig
Linear signal-to-concentration approximation (small enhancement).