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. You can open your DNA sequence files by clikcing on the DNA sample name. You can sort each column by clicking the header. In seconds, the program will generate a quality report which will open in your browser window. 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. Mac Sequence View With This program, you simply drag and drop your. ApE wiki for question, answers, feature requests, bug reports, etc.Sequencher is the industry standard software for DNA sequence analysis.ApE plasmid editor homepage & downloads.The current version, v2.0.46, doesn't have this issue, says bug report - JM 9/2013 Links to the ApE homepage Use with caution! - Damian Ekiert 12:19, 22 February 2013 (EST). See bug report here ('Misalignment of sequences with indels (sometimes)'). This should be corrected in the yet-to-be-released version 2.0.46. This can make it very easy to miss small deletions when checking your sequencing data against the expected sequence. In some cases where the sequences differ by a single base-pair indel, the alignment output by ApE is incorrect and the mismatching residues are not highlighted in red as expected. There is a serious bug affecting the alignment function in recent versions of ApE (I have encountered it in 2.0.39 - 2.0.45 at least, may affect all 2.0.X versions?) released over the last ~12 months, including the current release (2.0.45). The author is very responsive and integrated a BankIt export option, I suggested, within a few days. BLAST selected sequence at NCBI or wormbase.shows translation, Tm, %GC, ORF of selected DNA.restriction sites and region markup in sequence and in a simple cartoon.for primers, probes, or restriction sites pre-existing expandable feature tables which can be used for automatic annotation.export graphic files of sequence diagrams.exports BankIt feature table for sequence submission to NCBI GenBank.saves data in a modified Genbank file format (DNA Strider-compatible).imports DNA Strider, Fasta, Genbank, EMBL and ABI sequence traces.

Dna sequence viewer for mac