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> Assembly: selecting the optimal BioNano assembly Single molecule maps were assembled de novo into five distinct BioNano genome maps for T. castaneum.
A causal map was established to represent the causal knowledge of each of the experts and then, the established causal maps were assembled into a unique global causal map, which was subsequently validated by the experts.
In recent years, comprehensive human CNV maps were assembled using various experimental platforms [ 14- 16].
The single-molecule maps were assembled de novo into genome maps.
Using this scheme, 14 optical consensus maps were assembled having a total mass of 378.31 Mb.
Single-molecule maps were assembled de novo into consensus maps using tools developed at BioNano Genomics.
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These structures at the borders of the structure maps are assembled from different structural units with different physical properties.
For Hameroff and Penrose, the mediators of each protoconscious event are the proteinaceous dimers of tubulin which, together with their associated proteins (MAPs), are assembled into microtubules (MTs).
Next, each cluster of maps was assembled using the Gentig software to produce a contig (i.e., consensus restriction pattern) for the cluster.
F2-informative markers from each control F2 population (treatment F2 populations were not used in building the genetic map) were assembled into linkage maps under a standard F2 intercross design implemented in OneMap.
The EBV virus map was assembled de novo during the whole genome de novo assembly of the YH cell line genome.
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