To expedite marker development, Michelmore et al.[ 15] described the "bulked segregant analysis" (BSA) method, in which a small number of informative segregating individual plants (usually 20) are bulked to form two pools differing only for the selection region before conducting DNA fingerprinting for identification of candidate markers linked to the genes of interest.
The fingerprints of the candidates, most of them establishment figures, were stamped on forms, while would-be reformists stayed away.
Heinonen et al. [15] introduced FingerID, which uses a support vector machine to learn the mapping between the mass spectra and molecular fingerprints of the candidates.
By contrast, when NGS is used as DNA fingerprinting, the DNA sequences of candidate markers are known, and ready for primer design.
Pair-wise comparisons associated with co-expression analyses of DEGs defined a transcriptional fingerprinting of each cv with the detection of clusters of candidate loci responsible for some peculiarities characterizing the six varieties.
After identification of proteins by mass spectroscopy and fingerprint analysis, candidate proteins are scored and assessed individually.
SSR markers developed in this study have potential application to genomic research, marker-assisted breeding, DNA fingerprinting of genetic resources, molecular mapping of tree peony and related species, and map-based cloning of candidate genes.
Third, sets of candidate compounds for each transformation (having the reaction pattern) are characterized by a set of structural, stereo and fingerprint features.
Molecular fingerprints were predicted for each tree (with Platt probability estimates [34]) and compared against the fingerprints of all structure candidates (computed with CDK [30, 31]) with the same molecular formula.
Let (score(q_i, c_j) mid q_i in mathbb {Q} wedge c_j in mathbb {C}) be the Tanimoto score of the fingerprint of the query molecule at index i with the fingerprint of the candidate molecule at index j.
