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seqman pro 8.1.1  (DNASTAR)


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    Structured Review

    DNASTAR seqman pro 8.1.1
    Workflow followed for the individual assembly of different library/collections and for the assembly of different combinations of library/collections (e.g. assembly of libraries generated from the same tissue). Sections A and B show separate processes for both Sanger and 454 reads assembly. Different assemblies were performed using <t>SeqMan</t> Pro 8.1.1 except when assembling together all the reads generated, which was performed using a two-step assembly process (Newbler 2.6 followed by CAP3) to overcome problems when handling such large amount of data. QC Assembly stands for a quality control step carried out before the actual assembly, where all the reads matching any prokaryotic sequence were removed. QC Blast stands for a quality control step carried out for each assembly consisting of comparing the unigenes generated with themselves using BLAST to guarantee optimal assembly results.
    Seqman Pro 8.1.1, supplied by DNASTAR, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pro+lasergene+v8%2E0/seqman+software/pmc03576661-143-24-27
    Average 90 stars, based on 1 article reviews
    seqman pro 8.1.1 - by Bioz Stars, 2026-10
    90/100 stars

    Images

    1) Product Images from "De Novo Assembly and Functional Annotation of the Olive ( Olea europaea ) Transcriptome"

    Article Title: De Novo Assembly and Functional Annotation of the Olive ( Olea europaea ) Transcriptome

    Journal: DNA Research: An International Journal for Rapid Publication of Reports on Genes and Genomes

    doi: 10.1093/dnares/dss036

    Workflow followed for the individual assembly of different library/collections and for the assembly of different combinations of library/collections (e.g. assembly of libraries generated from the same tissue). Sections A and B show separate processes for both Sanger and 454 reads assembly. Different assemblies were performed using SeqMan Pro 8.1.1 except when assembling together all the reads generated, which was performed using a two-step assembly process (Newbler 2.6 followed by CAP3) to overcome problems when handling such large amount of data. QC Assembly stands for a quality control step carried out before the actual assembly, where all the reads matching any prokaryotic sequence were removed. QC Blast stands for a quality control step carried out for each assembly consisting of comparing the unigenes generated with themselves using BLAST to guarantee optimal assembly results.
    Figure Legend Snippet: Workflow followed for the individual assembly of different library/collections and for the assembly of different combinations of library/collections (e.g. assembly of libraries generated from the same tissue). Sections A and B show separate processes for both Sanger and 454 reads assembly. Different assemblies were performed using SeqMan Pro 8.1.1 except when assembling together all the reads generated, which was performed using a two-step assembly process (Newbler 2.6 followed by CAP3) to overcome problems when handling such large amount of data. QC Assembly stands for a quality control step carried out before the actual assembly, where all the reads matching any prokaryotic sequence were removed. QC Blast stands for a quality control step carried out for each assembly consisting of comparing the unigenes generated with themselves using BLAST to guarantee optimal assembly results.

    Techniques Used: Generated, Control, Sequencing

    Related Articles

    Sequencing:

    Article Title: Metabolic resistance to organophosphate insecticides in natural populations of the whitefly Bemisia tabaci (Hemiptera: Aleyrodidae) in Egypt and molecular identification of mitotypes
    Article Snippet: The whitefly Bemisia tabaci (Gennadius) (Hemiptera: Aleyrodidae) cryptic species has become an important pest of cotton and vegetable crops in Egypt.. In this study, resistance to three organophosphate insecticides (OPs), chlorpyrifos-methyl, profenofos and pirimiphosmethyl, and detoxification enzymatic activities of acetylcholinesterase, carboxylesterase, and monooxygenase were evaluated to establish baseline resistance levels for B. tabaci infesting cotton in seven Egyptian governorates, compared to a susceptible laboratory reference B. tabaci colony.. Resistance toOPs ranged from low-to-moderate or low-to-high, while detoxification enzymatic activities were predominantly governorate-dependent.



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