Base sequence analysis

From WikiMD's Wellness Encyclopedia

Base sequence analysis is a process used in molecular biology and genetics to determine the order of nucleotides within a DNA or RNA molecule. This sequence of nucleotides forms the genetic code that guides the development and function of living organisms.

Overview[edit | edit source]

The base sequence of a DNA or RNA molecule is the precise order of its nucleotides. Each nucleotide consists of a sugar, a phosphate group, and a nitrogenous base. The four types of nitrogenous bases in DNA are adenine, thymine, guanine, and cytosine, abbreviated as A, T, G, and C, respectively. In RNA, thymine is replaced by uracil (U).

Techniques[edit | edit source]

Several techniques are used in base sequence analysis, including:

  • Sanger sequencing: This method, developed by Frederick Sanger, uses chain-terminating inhibitors to produce DNA fragments of varying lengths. The fragments are then separated by electrophoresis, and the sequence is read from the lengths of the fragments.
  • Third-generation sequencing: This method sequences single molecules of DNA or RNA in real time, allowing for longer read lengths and the detection of modifications to the base sequence.

Applications[edit | edit source]

Base sequence analysis has numerous applications in various fields, including:

  • Genomics: It is used to sequence entire genomes, which can provide insights into the genetic makeup of organisms and help identify genes associated with diseases.
  • Phylogenetics: It is used to compare the base sequences of different species to determine their evolutionary relationships.
  • Forensics: It is used in DNA profiling to identify individuals or determine paternity.
  • Personalized medicine: It is used to identify genetic variations that may affect an individual's response to certain drugs.

See also[edit | edit source]

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Contributors: Prab R. Tumpati, MD