21-06-2016, 02:01 PM
02-07-2016, 02:06 PM
NEXT-GENERATION DNA SEQUENCING (NGS)
Sequencher empowers the benchtop scientist by bringing the latest peer-reviewed NGS algorithms out of the command line and into an intuitive point and click interface. Whether performing reference-guided alignments, de novo assembly, variant calling, or SNP analyses, Sequencher has the tools you need to get results. Sequencher has integrated the comprehensive Cufflinks suite for in-depth transcript analysis and differential gene expression of your RNA-Seq data. Sequencher can easily generate unique visualizations of your RNA-Seq data with custom plots and charts giving you publication-ready graphics in seconds.
SANGER DNA SEQUENCING
Sequencher's extensive Sanger analysis features are the foundation it was built upon. Customizable from start to finish there is no other program that offers you as much power as Sequencher. With an easy to use interface that has been honed over 25 years, first time users will feel like a pro in minutes. Everything from trimming reads, custom assembly and alignment algorithms, variation tables, summary reports, annotation; the list goes on and on. Come see why Sequencher has been published in tens of thousands of research articles, and peer-reviewed journals. Power with Simplicity.
A comprehensive workbench for advanced DNA, RNA, and protein analyses
The functionalities of CLC Main Workbench are used by tens of thousands of researchers all over the world for DNA, RNA, and protein sequence data analysis, such as gene expression analysis, primer design, molecular cloning, phylogenetic analyses, and sequence data management, amongst a wide variety of other features – all wrapped in an intuitive graphical user-interface.CLC Main Workbench is available on Windows, Mac OS X, and Linux platforms.Your research work will be easy to carry out as the program is graphically based, intuitive, and very user-friendly. You can also easily share your data with colleagues using our database solution, CLC Bioinformatics Database.The program continouosly evolves and frequent updates keep you up to date with the latest scientific developments.You can customize your workbench through our Software Developer Kit which allows you to develop and integrate features of your choice to the workbench.
Sequencher empowers the benchtop scientist by bringing the latest peer-reviewed NGS algorithms out of the command line and into an intuitive point and click interface. Whether performing reference-guided alignments, de novo assembly, variant calling, or SNP analyses, Sequencher has the tools you need to get results. Sequencher has integrated the comprehensive Cufflinks suite for in-depth transcript analysis and differential gene expression of your RNA-Seq data. Sequencher can easily generate unique visualizations of your RNA-Seq data with custom plots and charts giving you publication-ready graphics in seconds.
SANGER DNA SEQUENCING
Sequencher's extensive Sanger analysis features are the foundation it was built upon. Customizable from start to finish there is no other program that offers you as much power as Sequencher. With an easy to use interface that has been honed over 25 years, first time users will feel like a pro in minutes. Everything from trimming reads, custom assembly and alignment algorithms, variation tables, summary reports, annotation; the list goes on and on. Come see why Sequencher has been published in tens of thousands of research articles, and peer-reviewed journals. Power with Simplicity.
A comprehensive workbench for advanced DNA, RNA, and protein analyses
The functionalities of CLC Main Workbench are used by tens of thousands of researchers all over the world for DNA, RNA, and protein sequence data analysis, such as gene expression analysis, primer design, molecular cloning, phylogenetic analyses, and sequence data management, amongst a wide variety of other features – all wrapped in an intuitive graphical user-interface.CLC Main Workbench is available on Windows, Mac OS X, and Linux platforms.Your research work will be easy to carry out as the program is graphically based, intuitive, and very user-friendly. You can also easily share your data with colleagues using our database solution, CLC Bioinformatics Database.The program continouosly evolves and frequent updates keep you up to date with the latest scientific developments.You can customize your workbench through our Software Developer Kit which allows you to develop and integrate features of your choice to the workbench.