DNASTAR Published References

 

Publications graphic

 

DNASTAR is the worldwide leader in DNA sequence analysis software, and based on citations in peer-reviewed journals, it shows. Every year for the last 27 years, more researchers have cited DNASTAR's software in scientific journals than any other sequence analysis software.


To learn a few of the reasons why, see what our customers are saying:

"I've been using Lasergene for many years now and I love the simplicity of the program. It is easy to use and easy to teach students to use."
Sang-Jin Suh, Auburn University

"Lasergene is a fantastic software. It facilitates our researchers from the organization and analysis of samples, until the consolidation of results."
William Ferreira, Alfredo da Matta's Foundation

"I appreciated your sales staff - very responsive, but not obtrusive. This is very unusual!"
Thomas Besser, Washington State University

"SeqMan Pro is a great application for identifying gene mutations/polymorphisms. It is very reliable and easy to use."
Sevasti Koukouritaki, Medical College of Wisconsin

"Tech support is always helpful; even when the question needs to be researched."
Caprice Rosato, Oregon State University

"I have used the Lasergene package for years, and it is by far the best in the field. I love using SeqBuilder to make my plasmids organized and to plan my new cloning. MegAlign and SeqMan help me to sort out my sequencing outputs."
Mei Wu, University of Washington

"Always great customer service"
Philippe Couroux, Agriculture and Agr-Food Canada

"I particularly like about QSeq the fact that we can import both HTS and prior array data on the same samples to compare differences between the two technologies Secondly, I like how the unmapped reads can easily be assembled in SeqMan NGen to look for non-human ORFs in the sample."
Jay Kolls, LSU Health Sciences Center

"You make good stuff.  Keep it coming."
Mark Maffitt, Epicentre Biotechnologies

"ArrayStar is very simple to use and straightforward. Technical support is excellent!"
Jeeba A Kuriakose, University of Texas-Medical Branch

"I am very happy with SeqBuilder. It integrates nicely the need to construct and map plasmids."
Peter Nielsen, Max-Planck-Institute for Immunobiology

"We have used MegAlign to help identify short conserved motifs in orthologous genes with very low shared sequence similarity, and have gained great insight from these results."
John Allingham, Queen's University

 

To see a sampling of some these publications from 2010-2011, please view our Publications List.

(Based on data from Highwire, Stanford University.)