Sentence examples for most common genomic from inspiring English sources
The most common genomic imbalances were a gain of 14q, a loss of 16q, and a loss of 22q.
The most common genomic aberrations in this malignancy are the transcription factor fusion of TMPRSS2 ETS, and mutations in TP53, AR, RB1 and PTEN/PIK3CA.
In addition to the clinical advances in transcriptional subtyping, recent reports have characterized the most common genomic and epigenomic alterations that are likely to drive certain breast cancers.
The investigated banana varieties (Dwarf Cavendish, Prata, Maçã, Ouro and Platano) have certified botanical origin and belong to the Musaceae family, the most common genomic group cultivated in Madeira Island Portugall).
For climate adaptation, the most common genomic pattern is conditional neutrality, as proven by weak across-environment correlations, frequent SNP × environment interactions, and the topology of some developmental and physiological pathways potentially involved in local adaptation.
ETS-related gene (ERG) oncogenic activation is the most common genomic alteration in prostate cancer (CaP) although it occurs less frequently in African American (AA) versus Caucasian (CA) patients, and the potential role of ERG as a prognostic marker has not been confirmed.
The SNP rs1006737 in the gene CACNA1C is the most replicated and most studied common genomic variant associated with bipolar disorder to date.
Transposable elements are by far the most common genetic elements causing genomic variations in plants [ 17].
The reciprocal translocation t(12 21)(p13 q22), the most common structural genomic alteration in B-cell precursor acute lymphoblastic leukaemia in children, results in a chimeric transcription factor TEL-AML1 (ETEL-AML11).
The frequency of the causative deletion for 22q11DS in the general population is 1 in 3000 live births, making it one of the most common constitutional genomic alterations found in humans [ 7]. 22q11DS is suspected in individuals with characteristic clinical findings and is confirmed in most cases by detection of a sub-microscopic deletion using FISH.
These mice bear a ∼1 kb genomic deletion in the endogenous murine Cln3 gene that is analogous to the most common ∼1 kb genomic deletion in juvenile NCL patients.
