Your English writing platform
Discover LudwigExact(1)
This strategy provides a comprehensive description of satellite sequence variation and organization, revealing in addition both embedded transposable element insertion sites and adjacent non-satellite sequences that are often missing from current genome assemblies.
Similar(59)
Comparative genomics has provided valuable insights into the nature of gene sequence variation and chromosomal organization of closely related bacterial species.
Given this pattern, it is likely that the phenotypic differences are most attributable to changes in protein structure rather than in copy number variation and genomic organization.
All of these findings help to propose a useful and integrative conceptual non-linear model to discuss and quantify the structural variation and nonlinear organization of the human genome.
This level of genomic resolution requires both long- and short-range sequence information capable of capturing sequence variation and spatial organization within a single satellite array, between satellites occupying distinct chromosomal domains, and within a given population [ 13- 17].
In terms of copy number variation and gene organization, this is one of the most polymorphic regions of the human genome, and perhaps the single most polymorphic region of this type.
This is one of the most polymorphic regions of the human genome in terms of copy number variation and gene organization, and perhaps the single most polymorphic region of this type.
These variations in composition and organization in turn cause variations in mechanical properties of cortical bone.
Virtual erosion of myocytes revealed an extensive 3-D collagen network with qualitatively similar transmural variation in density and organization for WKY (Fig. 2 C ) and Wistar (Fig. 2 D ) rat hearts.
The functional identification and annotation of centromeres depends on the availability of two comprehensive and complementary sequence datasets: (i) a reference sequence database that describes all centromeric sequence variation and its underlying organization, and (ii) a functional sequence database that highlights the genomic features associated with centromere identity and function.
Microsatellite or simple sequence repeat (SSR) markers have been widely applied in quantifying the level of genetic variation and its spatial organization, describing the demography and history of populations, and analysing the gene flow and parentage in plants and animals (e.g. Arens et al. 2007; Smulders et al. 2008; Primmer 2009; Allan and Max 2010).
Write better and faster with AI suggestions while staying true to your unique style.
Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com