![]() To facilitate Sanger sequence analysis, many tools have been developed over the years, even as smartphone apps. 7 It is also routinely performed in general molecular methods in genetic engineering to generate. Sanger sequencing is used in primer walking, mass sequencing of error-prone PCR mutant libraries for protein engineering, 2, 3 in vitro reverse-transcriptase fidelity assays, 4 – 6 and prediction of host deaminases RNA editing sites. Although the capillary-based Sanger method is dated, it is still the gold standard given its superior accuracy and reliability over the second- and third-generation sequencing technologies ( i.e., next-generation sequencing, single-molecule real-time sequencing, etc.). The Sanger method, first developed by Frederick Sanger, 1 is widely used to generate accurate reads from homogenous samples economically. FASTQ sequencing reads de novo with automated trimming and scanning of the assembled sequences for single nucleotide polymorphisms and insertions or deletions without installation of software, allowing it to be accessed from anywhere with Internet access and with minimal dependency on other software and web tools. To facilitate such online accessible sequence assembly and analysis, we created Yet Another Quick Assembly, Analysis and Trimming Tool web server for the automated assembly of multiple. Through web servers with expanded automation and functionalities, even smartphones/phablets can be used to perform complex analysis previously limited to desktops, especially if they can upload files from cloud storage. With increased data output worldwide, there is also a need for automated quality checks and trimming prior to large assemblies, along with automated detection of mutations. Even with the ubiquity of Sanger sequencing, automated assembly software are predominantly stand-alone software packages for desktop/laptop use with very few online equivalents, thus geospatially constraining sequence analysis and assembly.
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