V březnu se zúčastníme celoslovenské genetické konference, která se koná 16. - 17. 3. 2022 v hotelu Turiec ve slovenském Martině. Konferenci pořádá Slovenská společnost lékařské genetiky a je již trad...
VíceNavštivte nás na Genetické konferenci pořádané Genetickou společností Gregora Mendela. Tento rok proběhne v termínu 5. - 7. 10. společně s konferencí Genetické dny, jež se konají ve dvouletých interva...
VícePřijďte se na nás podívat na Celostátní sjezd Společnosti lékařské genetiky a genomiky ČLS JEP a 55. výroční cytogenetickou konferenci, jež se koná ve Wellness Hotelu Step 15. a 16. září. Rádi se s Vá...
VíceEach software has more types of license available. 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) |
NextGENe is the perfect analytical partner for the analysis of desktop sequencing data produced by the ION PGM™, Roche Junior, Illumina MiSeq as well as high throughput systems as the Ion Torrent Proton, Roche FLX, Applied BioSystems SOLiD™ and Illumina® platforms. NextGENe software runs on a Windows® Operating System, which provides a biologist-friendly point & click interface, and does not require scripting or other bioinformatics support, often required when using programs such as CLC Bio, LaserGene, DNASTAR, MAQ,SOAP,Top Hat, BWA and Bowtie.
NextGENe software employs unique platform specific technologies in one free-standing multi -application package. NextGENe software contains analysis modules for SNP/INDEL & Structural Variant Analysis (resequencing & Amplicon analysis), Copy Number Variation (CNV), Prediction and Rare Disease Discovery; Whole Genome Alignment; Transcriptome; Alternate Splicing of Exons & Transcript Expression levels; RNA Seq; ChIP-Seq, Serial Analysis of Gene Expression (SAGE) analysis; Digital Gene Expression (DGE), Exome Assembly & Variant Discovery; miRNA Analysis & Quantification; Metagenomics; de novo assembly, CNV and Exome Capture.
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