The Journal Genomics & Gene Study is one of the most interdisciplinary fields of science that study of the full genetic complement of an organism (genome). It employs recombinant DNA, DNA sequencing methods, and bioinformatics to sequence, assembles, and analyse the structure and function of genomes.
Genetic engineering is the process by which scientists modify the genome of an organism. Creation of genetically modified organisms requires recombinant DNA. Recombinant DNA is a combination of DNA from different organisms or different locations in a given genome that would not normally be found in nature. In most cases, use of recombinant DNA means that you have added an extra gene to an organism to alter a trait or add a new trait. Some uses of genetic engineering include improving the nutritional quality of food, creating pest-resistant crops, and creating infection-resistant livestock.
The journal defines genomics as "diagnosis, prognosis, prevention and/or treatment of disease and disorders of the mind and body, using approaches informed or enabled by knowledge of the genome and the molecules it encodes." Relevant and high-impact papers that encompass studies of individuals, families, or populations are considered for publication. Emphasis will include coupling detailed phenotype and genome sequencing information, both enabled by new technologies and informatics, to delineate the underlying aetiology of the disease. Clinical recommendations and/or guidelines of how that data should be used in the clinical management of those patients in the study, and others, are also encouraged.
Genomics including genome projects, genome sequencing, and genomic technologies and novel strategies. Simple reports of single-mitochondrial, chloroplast and bacterial strain variant genomes are no longer suitable.
Functional genomics including transcriptional profiling, mRNA analysis, microRNA analysis, and analysis of noncoding and other RNAs using established and newly-emerging technologies (such as digital gene expression). Manuscripts analysing existing sequence data only are no longer suitable unless adding new sequence data or introducing a new algorithm for analysis. The algorithm must be made publicly available through a web page or as code.
Evolutionary and comparative genomics, including phylogenomics
Genomic technology and methodology development, with a focus on new and exciting applications with potential for significant impact in the field and emerging technologies
Computational biology, bioinformatics and biostatistics, including integrative methods, network biology, and the development of novel tools and techniques
Modern genetics on a genomic scale, including complex gene studies, population genomics, association studies, structural variation, and gene-environment interactions
Epigenomics, including DNA methylation, histone modification, chromatin structure, imprinting, and chromatin remodeling
Genomic regulatory analysis, including DNA elements, locus control regions, insulators, enhancers, silencers, and mechanisms of gene regulation
Genomic approaches to understanding the mechanism of disease pathogenesis and its relationship to genetic factors, including meta-genomic and the mode and tempo of gene and genome sequence evolution.
Medical Genomics, Personal Genomics, and other applications to human health
Application of Genomic techniques in model organisms that may be of interest to a wide audience.
RNA-seq experiments without three or more biological replicates will not be accepted for differential expression-based articles.
The journal is committed to providing an efficient publishing service to the community. An expert Editorial Advisory Board, independent editors and a streamlined peer-review system enable rapid and fair decision making through to publication. The final manuscripts will also be enhanced by the editorial process making them attractive and accessible to the broad readership of the journal.
Submit manuscript at https://www.imedpub.com/submissions/genomics-gene-study.html or send as an e-mail attachment to the Editorial Office at firstname.lastname@example.org
Fast Editorial Execution and Review Process (FEE-Review Process):
Journal of Genomics & Gene Study is participating in the Fast Editorial Execution and Review Process (FEE-Review Process) with an additional prepayment of $99 apart from the regular article processing fee. Fast Editorial Execution and Review Process is a special service for the article that enables it to get a faster response in the pre-review stage from the handling editor as well as a review from the reviewer. An author can get a faster response of pre-review maximum in 3 days since submission, and a review process by the reviewer maximum in 5 days, followed by revision/publication in 2 days. If the article gets notified for revision by the handling editor, then it will take another 5 days for external review by the previous reviewer or alternative reviewer.
Acceptance of manuscripts is driven entirely by handling editorial team considerations and independent peer-review, ensuring the highest standards are maintained no matter the route to regular peer-reviewed publication or a fast editorial review process. The handling editor and the article contributor are responsible for adhering to scientific standards. The article FEE-Review process of $99 will not be refunded even if the article is rejected or withdrawn for publication.
The corresponding author or institution/organization is responsible for making the manuscript FEE-Review Process payment. The additional FEE-Review Process payment covers the fast review processing and quick editorial decisions, and regular article publication covers the preparation in various formats for online publication, securing full-text inclusion in a number of permanent archives like HTML, XML, and PDF, and feeding to different indexing agencies.
Author(s): Asmaa Al-Fadil Hassan Khalifa
Inflammatory Bowel Disease (IBD) comprising Ulcerative Colitis (UC) and Crohn’s Disease (CD) is debilitating chronic immune disorder of the intestinal mucosa, multigenic in nature, resulting fro ... Read More
Author(s): Nigora Mavlyanova
Introduction: Fetal loss syndrome is a multifactorial disease characterized by a universal integrated response of the female body to any ill health in the pregnant woman, the fetus and the environment ... Read More
Author(s): Sarah Sabir
Statement of the Problem: Cousin Marriage is very common in part of world and there have been proven association with the degree of consanguineous marriages and prevalence of autosomal recessive genet ... Read More
Author(s): Sonali Bhattacharjee
DNA double-strand breaks are one of the most lethal lesions to a cell that can be repaired by one of the two cellular pathways; non-homologous end joining or homologous recombination. Homologous recom ... Read More