Sessions are saved and you may open saved Sessions at any time.
Sequencher Connections Completely Rewritten - You can now open more than one Connections Session of the same type at a time.Click on a bar or spot to see the underlying data highlighted. Viewing Cuffdiff Differential Expression Data and Plots - View the results of your RNA-Seq Differential Expression analysis as Volcano, Scatter, or Bar charts.Viewing Interim Cufflinks Data and Plots - Explore your interim Cufflinks genes.fpkm_tracking and isoforms.fpkm_tracking files using the new Bar Chart with links to the underlying data.Cuffdiff Advanced Options - Sequencher gives you access to all of Cuffdiff's command line options through its innovative GUI.Cuffdiff - Cuffdiff performs the analyses and statistical tests to find significant changes in expression, splicing, and promotor usage.Cuffmerge - You can merge Cufflinks assemblies using Cuffmerge prior to performing Differential Expression analysis.Cufflinks Advanced Options - Sequencher gives you access to all of the Cufflinks command line options through its innovative GUI.Cufflinks - You can now assemble RNA-Seq reads into transcripts from SAM or BAM files using Cufflinks.Cufflinks, Cuffmerge, and Cuffdiff Added to External Data Browser - We have extended the External Data Browser so that you can manage and annotate your RNA-Seq runs.New RNA-Seq Tools Installer - We have created a single downloadable installer to add all the components you need to perform RNA-Seq analysis.
RNA-Seq Differential Expression with Cufflinks Suite - You can now perform Differential Expression in Sequencher using Cufflinks.Pricing for Sequencer must be obtained by requesting a quote, which you can do here. It has many new capabilities that can reduce the time required to identify and validate heterozygotes and SNPs in your sequences. Sequencher capabilities include heterozygote and SNP detection and analysis, cDNA to Genomic DNA large gap alignment, comparative sequencing, support for confidence scores, ORF translation, GenBank feature import, and restriction enzyme mapping. Life Science researchers use Sequencher for many diverse DNA sequence analysis applications including de novo gene sequencing, mutation detection, forensic human identification, systematics, and more. First released almost 15 years ago, Sequencher is currently used for sequence analysis tasks in every major genomic and pharmaceutical company as well as numerous academic and government labs in over 40 countries around the world. It works with all automated sequencers and is widely known for its lightning-fast contig assembly, short learning curve, user-friendly editing tools, and superb technical support.
SEQUENCHER DNA SOFTWARE
Sequencher from Gene Codes Corporation helps you go from DNA sequence data to results easier and FASTER than ever! Almost 20 years of daily use by biologists in labs around the world have refined Sequencher's tools and interface.Sequencher is the industry standard software for DNA sequence analysis. Specialized tools for Forensic mtDNA profilingįor more information check out the Features page.Īre you frustrated that most bioinformatics software programs are hard to learn? Imagine DNA software that is so easy to learn and fast to use that you save hours a week, giving you more time in The Lab.What could you do with all that extra time?
Powerful Reference Sequence and the Variance Table find SNPs quickly and easily.Įxtensive data import & export capabilities, including customizable GenBank Feature handling Multiple, configurable DNA assembly algorithmsįull support of sequence data confidence values Sequencher is the biologists choice for DNA sequence Assembly and analysis software.
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