DNA sequencing
DNA sequencing is the method of sequencing the base pairs of a DNA (As, Ts, Cs, and Gs). Sequencing a whole organism’s DNA is a huge task. It needs breaking the DNA into several smaller items, sequencing the items, and collection of these sequences into one long "consensus."
These bases give the information on genotype and also the phenotype. Nucleotides aren't the sole determinants of phenotypes but are essential to their information. Every individual and organism feature a specific ester base sequence. DNA sequencing additionally underpins pharmacogenomics. This can be a comparatively new field that is leading to an individualized medication. Over a hundred and forty medication approved by the FDA currently by pharmacogenomic data in their labelling.
- DNA extraction
- DNA polymerase
- Epigenetics
- Recombinant DNA
- Restriction enzymes
- Sanger sequencing
Related Conference of DNA sequencing
DNA sequencing Conference Speakers
Recommended Sessions
- Advances in Molecular Diagnostics
- Biosimilar Monoclonal Antibodies
- Cellular and Molecular Biology
- Clinical Chemistry
- Clinical Diagnostics & Research
- DNA sequencing
- Immunogenicity Testing
- Infectious Diseases
- Integrative Molecular Medicine
- Metagenomics
- Molecular Biomarkers and Diagnosis
- Molecular Diagnostics
- Molecular Evolution
- Molecular Genetics and Genomics
- Molecular Medicine
- Molecular Oncology
- Molecular Pathology
- Next-Generation Sequencing
- Pharmacogenomics
- Point-of-Care Diagnostics
- Prenatal Molecular Diagnostics
- Stem Cell & Regeneration
- Translational and Molecular Medicine