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Polymerase Chain Reaction
Author(s) -
Gaurav Solanki
Publication year - 2012
Publication title -
international journal of pharmacological research
Language(s) - English
Resource type - Journals
ISSN - 2277-3312
DOI - 10.7439/ijpr.v2i3.514
Subject(s) - polymerase chain reaction , computational biology , applications of pcr , hot start pcr , in silico pcr , biology , inverse polymerase chain reaction , dna sequencing , multiple displacement amplification , polymerase chain reaction optimization , primer dimer , dna , multiplex polymerase chain reaction , genetics , computer science , gene , dna extraction

The polymerase chain reaction (PCR) is a technique in molecular biology to amplify a single or a few copies of a piece of DNA across several orders of magnitude, generating thousands to millions of copies of a particular DNA sequence. PCR is now a common and often indispensable technique used in medical and biological research labs for a variety of applications. There are three major steps involved in the PCR technique: denaturation, annealing and extension. PCR is useful in the investigation and diagnosis of a growing number of diseases. PCR is also used in forensics laboratories. PCR can identify genes that have been implicated in the development of cancer. The present paper is an attempt to review basics of PCR in relation to its methods, application and use.

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