Journal of Genome Research and Genetic Therapies (JGRGT) is a double-blind peer review Journal. Articles published by the Journal of Genome Research and Genetic Therapies are made copiously and evermore accessible online immediately upon publication that attributes elevated standard paper in Genome Research and Genetic Therapies. JGRGT is devoted to nourishing a systematic publishing service to the scientific world.

          Gregor Johann Mendel, the father of genetics who performed pea plant experiments, and demonstrated the actions of invisible "factors", now called Genes of an organism. The Genome is intended for an organism's whole set of DNA molecules. Studying the individual genes and their roles in the inheritance will come under Genetics. The Genome Research and Genetic Therapies focuses mainly on the structure, editing, mapping, evolution, and function of entire genomes.

Benefits of working with the Journal of Genome Research and Genetic Therapies:

  • Anyone can access our JGRGT which meant to be free, with no access fee, and unrestricted online open access to all the research outputs such as journal articles, Journal Newsletters and journal books.
  • Online - open access is compatible with double-blinded peer-review and selective submission standards are independent of the transparency of the Journal of Genome Research and Genetic Therapies.
  • In search operations, JGRGT could be easily traceable in order to find the article. To the greatest extent, searching the particulates in the articles or sharing it with social media or other scholars is facilitated.
  • Modes of Availability in our JGRGT, research words need not be constricted to articles only. It could be any type of digital proportion. This includes text, images, raw, audio, video, software, and processed data, which could be part of a digital archive.
  • The article-processing charge of JGRGT that covers a range of publishing amenity we present. This comprises a clause of online gadgets for eminent editors, prominent authors, article production, article hosting, associate to abstract with the notions of time, matter, and space, customer services, and indexing services. The processing charge is payable once your work is accepted by the editors and before the release.

Aim & Scope


1. To determine the function of the protein, used in Drug discovery, and on a large-scale protein engineering as well as protein structure.
2. To determine the biological functions of genes, Transcriptomics and Proteomics are the systematic and comprehensive pathway to study the normal and abnormal state of genes.
3. To characterize mutation associated genes, in cancer, we focus on Epigenomic and Transcript alterations, linking genotype to transcriptional state, finding of genes that underlying transcriptional changes.
4. To compare the basic biological similarities, differences, evolutionary relationships between the organism


Types of Testing: Molecular genetic test, Biochemical genetic test, Diagnostic testing, Clinical predictive test, Pharmacogenomic test, Tumor test, Chromosomal genetic test, Pre-symptomatic and predictive testing, Carrier testing, Prenatal testing, Preimplantation testing and Newborn screening.
List of Techniques: DNA Sequencing, RNA Sequencing, Sequencing Data Analysis, Methylation Sequencing, NGS Library Preparation, Human Genotyping with Arrays, Microarray Data Analysis, Non-Human Genotyping with Arrays, Methylation Array Analysis, Genotyping, Cytogenomics, Gene Expression Analysis, and Epigenetics.
Tools and Products: Automated DNA Extraction Systems, Magnetic Particle Processor, Automated DNA/RNA Purification Sample Preparation Workstations, Sample Management Software, DNA/RNA Purification Workstations, Protein Purification Workstations, Genotyping System/ Genotyping Instrument, Colony Pickers/ Colony Arrayers, Automated Electrophoresis Systems, DNA Microfluidics Chip Kits, Microarray Systems, Microfluidic Chip/ Microchip Electrophoresis Systems, DNA Sequencers/ Genetic Analyzers, Mass Spectrometers, Hybridization Ovens, Microarray Hybridization Chambers, Slide Hybridization Systems, Next Generation Sequencers, ChIP-Seq Kits, NGS Library Preparation and Sample Prep, Bisulfite Sequencing / Methyl-Seq Kits, RNA-Seq Kits, Epigenetics Tools.


  • Alleles and Genes
  • Deoxyribonucleic acid disorders
  • DNA Bio-chip
  • Molecular evolution
  • Genetic Engineering Tools
  • Precision Medicine and Genomics
  • Nucleic acid sequences
  • Molecular Genetics
  • Paleogenetics
  • Ancient Genome Duplications
  • Evolving Translation of Genetic Code
  • Abnormalities in Chromosome
  • RNA centered networks
  • Mutations in Hereditary
  • Human evolutionary genetics
  • Inheritable Diseases
  • Therapy in Genomics and Gene
  • Nuclear Genome
  • Archaeogenetics
  • Prokaryotic and Eukaryotic Genomes
  • Pseudogenes
  • Gene Mutation