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 »
“Learn about one and two-color microarrays and how and when they are used in expression studies. Explore the advantages, limitations and applications of one and two-color microarrays in this article.”
One-Color vs Two-Color Microarray- How to Choose the Right One? Read More »
