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Otherwise it was named "SHV-like" and its mutation profile was stored.
Otherwise, a new protein entry was created and its mutation profile was stored.
Subsequently, the mutation profile was matched against those mutation profiles listed in the TEM mutation table for the already assigned TEM β-lactamase sequences.
Subsequently, the mutation profile was matched against the mutation profiles listed in the SHV mutation table to identify whether the respective protein sequence is identical to an already assigned SHV.
The total number of implants diagnosed in each patient is displayed in the "number of implants" column and the count of how often each mutation profile was observed is specified in the "mutation profiles" column.
This BRAF mutation profile was chosen, as it is consistent with the genotype of the human tumours likely to be treated with BRAF-MEK1/2 signalling inhibitors in the clinic.
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This suggests that this mutation profile is the result of an endogenous mutational process for example, a defect in DNA repair that was acquired before the divergence of the two lineages, or that it was caused by independent exposure of the two lineages to a carcinogenic environmental agent.
The mutation profile is represented as a vector: v : S → ∑ ∪.
A typical comparison between the reconstructed and observed mutation profile is given in Figure S2B.
The main characteristics of the proposed patient mutation profile are as follows: Compact.
Then, for a given mutation profile v its corresponding binary mutation profile is defined as follows: b (s ) = ?
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