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SnapGene Viewer is described as 'Is revolutionary software that allows molecular biologists to create, browse, and share richly annotated DNA sequence files up to 1 Gb in length' and is a DNA Editor in the sport & health category. There are more than 25 alternatives to SnapGene Viewer for a variety of platforms, including Windows, Mac, Linux, Web-based and SaaS apps. The best SnapGene Viewer alternative is VectorBee, which is free. Other great apps like SnapGene Viewer are Benchling, BioEdit, Chromas and UGENE.
DrugPatentWatch provides deep knowledge on pharmaceutical drugs - patents, suppliers, generics, formulation, and more.
Ridom TraceEdit is a cross-platform graphical DNA trace viewer and editor. TraceEdit displays the chromatogram files from Applied Biosystems automated sequencers and files in the Staden SCF format.

Scientific software for the molecular biologist. Performs virtual DNA cloning, analyses DNA for restriction enzymes, homing enzymes and primer sites, dam and dcm methylation sites, finds and translates open reading frames. Calculates annealing temperatures for PCR.




GENtle is a software for DNA and amino acid editing, database management, plasmid maps, restriction and ligation, alignments, sequencer data import, calculators, gel image display, PCR, and much more.




The Snthesis Bio platform automatically integrates and harmonizes all your research data. Source agnostic. Search everything.


Use SimVector to draw plasmid maps, perform restriction analysis and mapping. The plasmid drawing software also simulates cloning experiments such as gateway cloning, ta cloning and restriction cloning



VectorFriends combines various types of cloning simulations, sequence analysis and data management into one application.

HistoAtlas is a comprehensive resource mapping the morphological landscape of cancer across 21 TCGA cancer types. By extracting quantitative histological features from over 6,000 diagnostic whole-slide images, HistoAtlas reveals how tissue architecture relates to patient...




QIAGEN CLC Main Workbench is ideal for DNA, RNA, & protein sequence data analysis with a wide variety of features, no advanced computer skills required! The workbench is available for Windows, Mac OS X, and Linux platforms.

Complete bioinformatics toolkit for a wide range of genomics analysis needs, including transcriptomics, variant calling, epigenomics, metagenomics, comparative genomics and many more.