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Published Papers

Name User Opinion
1 The Johns-Hopkins School of Medicine Professor Bert Vogelstein, world-renowned genetist in colon cancer, the most cited author in the world, and the member of US Academy of Sciences.
John Hopkins Oncology Center
Howard Hughes Medical Inst.
1650 Orleans Street, Room 589
Phone: 410-955-8878
Fax: 410-955-8886
Email: vogelbe@welch.jhu.edu

 
"I have examined its design and feel that is both innovative and powerful, and represents a substantial advance over other algorithms that are currently available for this purpose. I believe it could substantially enhance the accuracy and efficiency of our mutation analysis."

 
2 Celera Genomics Dr. Mark D. Adams,
Vice President of Celera Genomics Inc.

45 W. Gude Dr.
Rockville, MD 20850
Phone: 240-453-3700
Fax: 240-453-3755
Email: Mark.Adames@celera.com


"I am writing in support ´ to develop software for detection and basecalling of heterozygous positions in DNA sequence files. This problem is one of the last remaining hard problems of basecalling in the world." " Your efforts to deconvolute these two signals, guided by template sequence from human genome, for example, offer the opportunity to recover this data and take better advantage of it for detecting and typing indel polymorphisms."
 
3 The Dana Farber Cancer Institute William R. Sellers, MD
Paez Guillermo, M.D.
Dana Farber Cancer Institute
44 Binney Street
Dana 720C
Boston, MA 02115
USA
office phone: (617) 632-5261
fax: (617) 632-5417
e-mail: william_sellers@dfci.harvard.edu
"The software really works for our research so we bought the software." said Dr. Guillermo, "It is the best software available and it is easy to use."
 
4 National Cancer Institute, NIH, Advanced Technology Dr. Victor Llaca
High-Throughput Genome Analysis Center, NCI Advanced Technology Center
"We liked the software. It detects mutations with great confidence when it is blue color. The mutations with red color are frequently wrong."

 
5 SAIC-Frederick Dr. Shirley Tsang
915 Tollhouse Road, Suite 211
Frederick, MD 21702
Ph. 301-846-6213
Fax: 301-846-6100
Email: shirleytsang@ncifcrf.gov
"The software comes at the right time and right price to solve our needs."

 
6 Ingenium Pharmaceuticals
 
Dr. Thomas Peters
Scientist Genomics
Fraunhoferstraße 13
82152 Martinsried - Germany
phone: +49 (0)89 8565-2323
fax: +49 (0)89 8565-2351
thomas.peters@ingenium-ag.com
http://www.ingenium-ag.com
"This Version works excellent. So far the mutation report has detected all of our heterozygous mutations. Overall we realized that Mutation Surveyor is completely equivalent to the Polyphred software that we usually deploy for mutation detection. However, Mutation Surveyor is much more comfortable for our analysis because the software can easily be handled and it works on windows (not on Linux like Polyphred)."

 
7 MedGen, The Netherlands
 
Jacob Hofman-Bang, Ph.D.
Molekylær biolog Statens Serum Institut
"Having tried the software, I like it enough to enquire the price for 1, 3, 5, 7, and 10 users. I am in the academic world."

 
8 Professor Henrik Dahl
A/Prof. Henrik Dahl
Head of Gene Identification and Expression

The Murdoch Childrens Research Institute
Royal Children's Hospital
Flemington Road, Parkville
Melbourne, Vic. 3052
AUSTRALIA

Phone: +61-3-8341 6253
Mobile: 0409 223 326
FAX: +61-3-9348 1391
Email: dahl@cryptic.rch.unimelb.edu.au
http://murdoch.rch.unimelb.edu.au
"We are very, very impressed by it. It certainly is much better than any of the other programs that we use. It is partly because it is so easy to compare two sequence reactions and because it appears excellent in calling heterozygous mutations."