
Na jaře se zúčastníme 1. československého kongresu lékařské genetiky, který se bude konat 2.-4. dubna 2025 v Kulturním a kongresovém centru Elektra v lázeňském městě Luhačovice. Tento jedinečný kong...
VíceNavštivte nás na 19. ročníku konference RANK 2025, která se koná 19. a 20. března v hotelu Zlatá Štika v Pardubicích. Konferenci pořádá Česká společnost klinické biochemie při ČLSJEP ve spolupráci s ...
VíceRádi bychom Vás pozvali na 23. Kaprasův den na téma „Klinická genetika“, který se uskuteční ve středu 26. února 2025 v Kongresovém sále Hotelu Olšanka v Praze. Těšíme se na setkání s vámi a na den pln...
VíceEach software has more types of license available. The price of software is influenced by more factors. Once you buy the software, it works permanently, but you can also buy additional technical support for receiving updates and for getting technical assistance. There is a table of product possibilities:
Standalone Program and single user license |
Network Version and single user license |
Site License |
Additional User licenses for Standalone program |
Additional user licenses for Network version |
Annual technical assistance and update subscription for basic license |
Annual technical assistance and update subscription for additional licenses (each) |
GeneMarker® software is a unique genotype analysis software which integrates new technologies enhancing the speed, accuracy and ease of analysis. Biologist-friendly, the software is an excellent alternative to Applied BioSystems Genotyper® and GeneScan® or GeneMapper® software; LiCor's SAGA, MegaBACE® Genetic Profiler and Fragment Profiler, SeqencePilot®, or MRC Holland's Coffalyser.Net software. Compatible with outputs from all major sequencing systems i.e. ABI®PRISM, Beckman-Coulter®, and MegaBACE® platforms the software's Windows® based operation (XP,Vista 7 or 8) simplifies such applications as Amplified Fragment Length Analysis (AFLP®), t-RFLP, SSR (short sequence repeat) and Microsatellite Analysis, any genotyping application. GeneMarker software includes integrated modules for MLPA®, MS-MLPA, LOH, SNapShot®, SNPlex®, SNPWave®, TILLING® (Targeted Induced Local Lesions in Genomes), Microsatellite Instability (MSI), Haplotype Analysis, Trisomy, as well as Cystic Fibrosis Analysis utilizing chemistries from GeneProbe®, MRC Holland, Abbott Diagnostics and others, Fragile X from Asuragen® and custom chemistries. Incorporated tools include Kinship Analysis of Wild Populations; Phylogeny Clustering; Project Comparison; as well as a User Management providing an analysis audit trail and editing.