QUICK LINKS
SUPPORT
©1994- PREMIER Biosoft. All rights reserved.
Home >> Products >> MLPA Designer >> Citations & Reviews
Title/Description |
Author and Details |
Year |
| Improving Mutation Screening in Familial Hematuric Nephropathies through Next Generation Sequencing | Morinière, V., Dahan, K., Hilbert, P., Lison, M., Lebbah, S., Topa, A., Bole-Feysot, Christine., Pruvost, Solenn., Nitschke, Patrick., Plaisier, Emmanuelle., Knebelmann, Bertrand., Macher, Marie-Alice., Noel, Laure-Hélène., Gubler, Marie-Claire., Antignac, Corinne., Heidet, Laurence. (2014) J Am Soc Nephrol, 25(12), 2740–2751. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4243343/ |
2014 |
Germ-line deletion in DICER1 revealed by a novel MLPA assay using synthetic oligonucleotides |
Sabbaghian, N., Srivastava, A., Hamel, N., Plourde, F., Gajtko-Metera, M., Niedziela, M., Foulkes, W.D. (2014). Eur J Hum Genet, 22(4), 564-7. |
2014 |
Gain of 1q is associated with inferior event-free and overall survival in patients with favorable histology Wilms tumor: A report from the Children's Oncology Group |
Gratias, E. J., Jennings, L. J., Anderson, J. R., Dome, J. S., Grundy, P., & Perlman, E. J. (2013). Cancer, 119(21), 3887-3894. |
2013 |
A 5.8 kb deletion removing the entire MNX1 gene in a Norwegian family with Currarino syndrome |
Holm, I., Monclair, T., Lundar, T., Stadheim, B., Prescott, T. E., & Eiklid, K. L. (2013). Gene, 518(2), 457-460. |
2013 |
Identification of recurrent type-2 NF1 microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorder |
Vogt, J., Mussotter, T., Bengesser, K., Claes, K., Högel, J., Chuzhanova, N., ... & Kehrer‐Sawatzki, H. (2012). Human mutation, 33(11), 1599-1609.
|
2012 |
BeeDoctor, a Versatile MLPA-Based Diagnostic Tool for Screening Bee Viruses |
De Smet, L., Ravoet, J., de Miranda, J. R., Wenseleers, T., Mueller, M. Y., Moritz, R. F., & De Graaf, D. C. (2012). PloS one, 7(10), e47953. http://www.plosone.org/article/info%3Adoi%2F10. |
2012 |
Two New Rapid SNP-Typing Methods for Classifying Mycobacterium tuberculosis Complex into the Main Phylogenetic Lineages |
Stucki, D., Malla, B., Hostettler, S., Huna, T., Feldmann, J., Yeboah-Manu, D., ... & Gagneux, S. (2012). PLoS One, 7(7), e41253. |
2012 |
Four unrelated patients with lubs X-linked mental retardation syndrome and different Xq28 duplications |
Bartsch, O., Gebauer, K., Lechno, S., Van Esch, H., Froyen, G., Bonin, M., ... & Haaf, T. (2010). American Journal of Medical Genetics Part A, 152(2), 305-312. http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.33198/full |
2010 |
MLPA® Designer automates the design of highly specific synthetic oligos for MLPA assays. MLPA® (Multiplex Ligation dependent Probe Amplification) is a simple, high throughput multiplex PCR technique introduced by MRC-Holland that allows detection of abnormal copy numbers of up to 50 different genomic DNA or RNA sequences. This easy to perform technique requires the use of a thermocycler and capillary electrophoresis equipment. MLPA® Designer strictly adheres to the guidelines laid by MRC-Holland for designing of MLPA® oligos.
You can organize data of multiple experiments by creating separate projects for each of them. This functionality helps you to maintain a local database for sequence information and search results. There is no limitation to the number of projects that you can create using the program.