The phrase "a subset of genomic" is not correct as it is incomplete.
It can be used when referring to a specific portion or category within the broader field of genomics.
Example: "The study focuses on a subset of genomic data related to rare genetic disorders."
Alternatives: "a portion of genomic" or "a segment of genomic".
Although a linkage map has recently been published (Criscione et al. 2009), it only provides information for a subset of genomic scaffolds and disagrees substantially with the genome assembly map.
Yet, many biological questions can be addressed by describing polymorphisms from a subset of genomic regions, provided that these regions are approximately evenly distributed throughout the genome.
DDM1 also contributes to the maintenance of CHG and CHH methylation in a subset of genomic sequences [39], [49].
For our study, enrichment was obtained by a "data-based strategy" of searching for conserved sequence only within a subset of genomic sequence that had already been collated in stem-cell transcript libraries [SCGAP].
As a proof of concept that DNA methylation in a subset of genomic loci may connect end-stage cardiomyopathy with different etiologies, we set out initially to profile a series of heterogenous cardiomyopathic left ventricles and a single normal control (diseased: samples I, II, III; control: sample A; Table 1) using MeDIP-chip (Method summarised in Figure S1).
For instance, the majority of the reads at the SPAC10F6.15 locus were mapped to the Crick strand whereas the annotated transcript is on the Watson strand (Supplementary information file, Figure S6), indicating that antisense expression might be dominant for at least a subset of genomic regions.
We present direct evidence that, for a subset of loci, genomic DNA from differentiated cortical neurons undergoes methylation changes during the course of maturation and aging.
We further validated association of c-Myc with a subset of the genomic loci identified in our ChIP-chip experiments by employing qChIP-PCR in four independent experiments with c-Myc antibody, carried out using two different ES cells lines (AK7 and R1) (Figure 1B, Figure S2).
However, despite CTCF and Dali thus occupying a subset of shared genomic binding sites, UV-RIP provided no evidence of a direct physical interaction.
A subset of recurrent genomic imbalances suggested involvement of known cancer associated genes in HS pathogenesis, including deletions of the tumor suppressor genes CDKN2A/B, RB1 and PTEN.
It is noteworthy that a subset of the genomic similarities between the SCLC and NSCLC cell lines could be the result of adaptation to culturing conditions.
