Sentence examples for genomic shared from inspiring English sources
The pre-publication history for this paper can be accessed here: http://www.biomedcentral.com/1471-2407/12/293/prepub We acknowledge the Pathology Core facility for providing human primary tumor specimens including TMAs and Genomic Shared Resources for gene expression assay at Roswell Park Cancer Institute.
Genetic linkage results in the preservation of homozygous segments in the genome that are produced as the result of genomic sharing, which can then be detected as runs of homozygosity (ROH).
It also allowed us to identify conserved genomic features shared by all A-genome or D-genome species and accessions.
The homologous genomic regions shared between two genomes are represented by a mean of identity values [ 18, 19].
In order to compare our genomic dataset, it was fundamental to identify a common and unique genomic feature shared by all 21 Thermococcales genomes under study.
We may speculate that kinship estimated based on marker data can reflect the true unobserved genomic sharing better then the expectation computed from even a correct pedigree.
We also looked at genomic sharing in pairs of individuals with or without at least one inbred LCA.
We focus on identifying specified pedigree relationship from actual or realized genomic sharing, for example, whether a pair of individuals are related either as second cousins or as cousins once removed, in each case assuming there is uniparental sharing.
Follow-up two-pedigree pSGS analyses further indicated excessive genomic sharing across the pedigrees in all three regions, suggesting that the underlying susceptibility alleles in those regions may be shared in common.
Unlike typical GWAS, in which the effects of single SNPs are calculated independently, GCTA evaluates the relative levels of genomic sharing between individuals, creating a GRM and associating this relatedness to quantitative trait variation or binary trait risk.
After sorting based on the genomic locations of CNVs, genomeCoverageBed was run to define the common genomic regions shared by patients' CNVs, named overlapping regions.
