Sentence examples for a valid matching from inspiring English sources

Exact(2)

Then X∪ e M =(p M, p M′) is a valid matching with weight at least w(M∗ /2.

For a maximum flow f in N, define the set of pairs M f   = {(x, y) :  x ∈  X, y ∈  Y X, f x, y) = 1}.From flow conservation constraints, it is simple to assert that every z ∈  X ∪  Y participates in at most one pair in M f, and thus M f  is a valid matching, and in addition, M f   ⊆  X ×  Y X.

Similar(58)

The purge itself required sensitive judgment calls, notably when to regard a name on a list of convicted felons as a valid match with a name on the voting rolls.

The 40% criterion should prevent intron sequence in the read from disallowing a valid match while still providing sufficient specificity.

We collated all SAGE tags with a valid match to a gene and ranked each gene according to how many times it was tagged.

For subjects without a valid match and for all others without specific cause of death, efforts were made to obtain a death certificate.

There were 1251 cases of KS in the TCR data and 1017 (81%) had a valid match to a person in the CDSC data reported from anywhere in the UK.

There were 516 people from the CDSC data with Burkitt's lymphoma or immunoblastic lymphoma and a first report from a region located wholly or partly within the TCR catchment area, and 228 (44%) had a valid match to an NHL record from the TCR data.

There were 2079 people from the CDSC data with presumptive or definitive KS and a first report from a region located wholly or partly within the TCR catchment area and 648 (31%) had a valid match to a KS record in the TCR data.

UFO also uses a high-dimensional word-based feature space [ 11] according to a word length of 20 amino acids, but in addition the discriminant scores of the five highest scoring domain families are passed to a small neural network to decide whether a score actually indicates a valid match.

After the alignment to the reference genome about 40% of the initial reads was excluded from further analysis because: (1) lacking a valid match on the reference genome (6% on average); or (2) because these reads were vector-only sequences (21% on average); or (3) repetitive elements that could not be univocally mapped to the reference genome (13% on average).

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