Sentence examples for variants and phenotypes from inspiring English sources
Ultimately, differences in expected lifespan among individual genotypes will be resolved by the joint processes of gene identification, characterization of molecular mechanisms, and associations between specific variants and phenotypes.
5 Known genetic causes of infertility include chromosomal aberrations, single gene variants, and phenotypes with multifactorial inheritance.
In summary, the SwissVar portal provides a unique environment and search facility to investigate the relationship between human variants and phenotypes, with a particular focus on human proteome.
We should not anticipate one-to-one relationships between allelic variants and phenotypes, be they traditional behavioral measures or neurobiological endophenotypes (Flint & Munafò 2007).
The results from all these new data are tantalizing - on the one hand we now have extensive, reliable information on the associations between particular genetic variants and phenotypes.
17, 31 In the 1990s, this type of research became very popular and many studies analyzing the relationship between genetic variants and phenotypes were published, although their main findings were often difficult to replicate.
Several recent sequencing studies provide additional evidence for this relationship between predicted functional variants and phenotype [30], [33], [34], [39].
Considering complex relationship between variants and phenotype, simultaneous variable selection using the whole chromosome would be the most appropriate approach.
They argue that searching for QTNs holds little value in that such research focuses on patterns (e.g. genomic signatures of selection or statistical associations between sequence variants and phenotype) rather than the evolutionary process itself.
DECIPHER (DatabasE of genomiC varIants and Phenotype in Humans Using Ensembl Resources) is an international community of academic departments of clinical genetics and rare disease genomics that together have deposited genomic variants and phenome data from more than 14,450 cases for which consent has been given for public display [ 7].
The association between this variant and phenotype is population-specific, that is, it appears in AAs, but not in EAs.
