A possible role of DNA sequence-specific electromagnetic resonances in the formation of the morphogenic field is discussed. It is proposed that the morphogenic field is formed by resonant oscillations of delocalized electron and proton clouds in the base stack of the DNA. Models are proposed for DNA sequence-dependence of possible electromagnetic resonance patterns. It is proposed that genomic repeats act as universal resonators providing the bidirectional communication between the chromatin structure and the morphogenic field. It is proposed that genomic repeats participate in two major functions - the morphogenic function and the brain function. It is proposed that microtubules mediate the resonance communication between the action potential in axons and genomic repeats in the nucleus. The existence of an algorithm is proposed responsible for the conversion of genomic information into the shape of the body. Such an algorithm is named the DNA resonance code. It is proposed that the DNA resonance code can be deciphered by targeted efforts in biophysics, spectroscopy, molecular modeling, and experimental genomics. A possible resonance interaction between the DNA of neurons and neuronal firing is discussed and it is suggested that deciphering the DNA resonance code may be of help to deciphering the neuronal coding in the brain. It is suggested that the deciphering of the DNA resonance code would benefit medical applications related to morphogenesis and brain function

lu, transposon, microtubules, biofield, morphogenetic field, morphic resonance, biological development