First, we are exploring procedures to empirically validate our method for associating diseases with proteins.
This research provides the first method for associating the personal genome with diseases with regard to genome-sequencing studies.
Herein we present a method for associating the personal genome with diseases based on the relative closeness between the personal genome and diseases.
However, by discounting the widely accepted scientific method for associating cause and effect (while taking into account the uncertainties of dose assessment and measurement of impacts), the authors leave us with only with their assertion that the data in this volume "document the true scale of the consequences of the Chernobyl catastrophe".
DNA barcoding and other DNA sequence-based techniques for investigating and estimating biodiversity require explicit methods for associating individual sequences with taxa, as it is at the taxon level that biodiversity is assessed.
Method: We present novel methods for associating pathway model reactions with relevant publications.
A new method for constructing associated multiwavelets from multi-scaling functions is presented which is simple for computation, need not solve a set of nonlinear equations in unknown matrices or correspondingly factorize a polynomial matrix into a special form, and is not restrained by the multiplicity of multiwavelets.
Methods: We present two novel methods for identifying associated pathways.
Specific gaps in available test methods for mechanisms associated with breast cancer include progesterone receptor binding (Brisken 2013) and transcriptional activation (Faivre et al. 2008; Kougioumtzi et al. 2014), Her2 activation (Stern 2008), ERβ activity (Pearce and Jordan 2004), and DNA repair mechanisms (Barnes and Camplejohn 1996).
Thus, our proposed method, a novel strategy for associating two data categories, is capable of integrating information from different sources to identify reliable candidate regulatory SNP-containing motifs introduced by genetic variation and mutation.
