| http://www.w3.org/ns/prov#value | - The other four lanes contain probe sets for detecting all possible single-base mutations in the defined sequence; in turn, these probe sets are defined by a position of potential non-complementarity in the probe relative to the target (i.e., a single base mismatch) and the identity of the nucleotide in the probe at that position (i.e., whether the nucleotide is an A, C, G, or T nucleotide).
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