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        • Personalised Cancer Therapy
        • Revolutionising human-like-protein production
        • The Microbiome Of Cancer
        • All about biomarker discovery
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        • Plant Breeder
        • DNA marker discovery
        • Marker-assisted selection
        • GRAS-Di®
        • Microbiome and metagenomics
        • Animal Breeder
        • DNA Marker discovery
        • Pathogen screening
        • Parentage testing
        • Genomic selection
        • Marker-assisted selection
        • Webshop - GenFarmEval
        • Favorite Content
        • Microarrays Accelerate Blue Biotechnology
        • How To Do NGS 50% Faster
        • NGS Portfolio

        • GenFarmEval.com

          Visit our Webshop for Farmers

          learn more

    • Consumer Genomics
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        • Genotyping
        • Epigenome Profiling
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        • Shotgun Sequencing
        • Whole Genome Sequencing
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        • Favorite Content
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        • The End of Gene Doping
        • Home Genomics Testing
        • IVDR Compliance
    • Food & Environment
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        • Food Testing
        • Food Authenticity
        • Meat Traceability
        • Pathogen Traceability
        • Cannabis and Hemp Testing
        • Environmental Testing
        • Non-targeted detection of organisms / species
        • Targeted detection of organisms / species
        • eDNA Tracker
        • Favorite Content
        • Determine the Source of Meat
        • Pine Nuts – Why Testing For Edibility Matters
    • Diagnostic Kit Producer
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        • Large Scale Oligos
        • Special Requests in Tubes
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        • The Future of RNA Applications
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        • TubeSeq Service Sanger
        • INVIEW Microbiome NGS
        • NGS Services
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        • Mix2Seq NightXpress
        • Express Genes
        • Express GeneStrands
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        • Eurofins Genomics Goes Green
        • GENEius – Codon Usage Optimisation
        • 5 tips to speed up your qPCR
        • Why salt-free oligos are the unsung hero of molecular biology
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FAQs Sanger Sequencing


contig

A contig is the result of the assembly process, consisting of contiguous DNA sequences/ sequencing reads and not interrupted by unknown regions.

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