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Rapid advancements in genome sequencing technologies have enabled the establishment of new model species with novel morphological and developmental features that enable the generation of chimeric organisms.
This has led to the investigation of the dedifferentiation and genetic reprogramming associated with SE, using advances in gene technology and model species with sequenced genomes.
The development of model species with genetic and bioinformatic tools has advanced the field and holds potential for further characterizing and engineering of methanogenesis.
Understanding molecular mechanisms of toxicity is facilitated by experimental manipulations, such as disruption of function by gene targeting, that are especially challenging in non-standard model species with limited genomic resources.
No single species is more enriched for "interesting" genes than any other species, but the traditional tractability of studying these interesting genes was centered on the model species with excellent molecular, physiological, biochemical, cell biological and genetic toolkits.
To address this challenge, we developed a method for transcriptomic and proteomic comparison and demonstrate its utility for use on a model species with value to physiology and endocrinology but having limited genomic information.
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We expect that these relationships can be used to predict the anticipated exon-intron structure and proteomic complexity in non-model species with large genomes, such as pines, that may remain unsequenced for a while.
A range of high-throughput methods are currently developed for model species such as humans, but their use in non-model species with large genome size, high level of ploidy or redundancy is often a challenge [22].
The significance of epigenetic changes and the study of non-model species with next-generation DNA sequencers is also discussed.
The results of this study have important implications for SNP discovery in non-model species with ancestrally duplicated genomes.
However, in non-model species with poorly characterized genomes, it may not be apparent if relative gene expression is responsible for an interesting phenotype.
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