What should be the key requirement to perform any molecular genetic experiment in which DNA is involved? Your answer will be ‘DNA’, Right? Let me tell you that you are […]
How to Improve Your PCR or qPCR Results? [Skills assessment] Read More »
Do you know a typical NGS machine can generate around 1.8 to 6TB of sequencing data in a single run? PCR duplication is a serious problem in so many crucial
Emulsion PCR: Principle, Process, Advantages, Applications and Limitations Read More »
“False positive and false negative results in PCR are two critical problems. In this article, learn about these two common PCR errors, how it occurs, and how to overcome them.”
PCR Troubleshooting 104: Understanding False Positive and False Negative PCR Results Read More »
“Primer dimers are unintended short amplification products formed in the PCR by unhealthy PCR practices. This article covers common causes for primer dimer formation and troubleshooting.” In the previous article
PCR Troubleshooting 103: How to Address Primer-Dimers Read More »
“Detergents play a crucial role in any DNA extraction scheme and thus have pivotal importance. This article focuses on the role and types of detergents used in DNA extraction.” Do
What is the role of Detergents in DNA extraction? Read More »
“Whole genome and whole exome sequencing are two NGS platforms that can investigate the entire genome and coding sequences, respectively. Learn about the common and technical differences between WGS and
Differences Between Whole Genome vs Whole Exome Sequencing Read More »
