CNV Backbone Spike-in Panels

Twist CNV Backbone Spike-in Panel with exome for cytogenetic research
Stronger CNV Detection — Without Changing Your Exome Workflow.

Large copy number variations can be easy to miss when exome sequencing focuses on exonic regions – leading to blind spots, repeat testing, and extra time interpreting unclear data. By spiking in Twist’s CNV Backbone Panels, you give your exome run the evenly spaced genomic coverage it needs to reliably surface clinically relevant CNVs — especially the ones standard exomes struggle with.

Available in 100 kb, 50 kb, and 25 kb resolutions, the CNV Backbone Panels strengthen your detection sensitivity while keeping your workflow identical. Blend it into your existing exome panel, follow your standard Twist enrichment protocol, and immediately get more confident CNV calls backed by consistent probe tiling across intergenic regions.

But... Why These Panels?

1. Fine-Tune CNV Resolution

Choose from 100 kb, 50 kb, or 25 kb probe spacing to match your CNV detection needs. Strategically tiled probes in intergenic regions enhance sensitivity for even small CNVs.

2. Seamless Workflow Integration

Easily spike into your Twist Exome 2.0 panel and follow standard enrichment protocols—no workflow disruption, no extra training required.

3. Evidence-Based Performance

Validated with highly characterized samples, the panels consistently improve CNV calls, including those smaller than 50 kb, boosting confidence in your results.

4. Flexible Panel Sizes

Available in 2-reaction (16 samples) and 12-reaction (96 samples) formats to fit both small-scale research and high-throughput lab workflows.

Download Poster on utilization of these panels with exome for cytogenetic research

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    Why It Matters to You

    Reliable CNV detection isn’t just a technical metric—it directly impacts research outcomes, diagnostic accuracy, and patient care. Standard exome sequencing often misses CNVs due to uneven probe coverage, creating blind spots in your analysis. Twist CNV Backbone Spike-in Panels bridge those gaps, ensuring that even subtle copy number changes are identified, so you can make confident, data-driven decisions.

    For labs and clinicians, this means fewer follow-up tests, reduced time spent troubleshooting ambiguous results, and a smoother workflow. You can trust that your exome sequencing captures the variations that truly matter, whether for rare disease research, clinical diagnostics, or high-throughput screening.

    Moreover, the ability to choose between 25 kb, 50 kb, or 100 kb resolution gives you control over sensitivity and throughput, aligning with your project goals and patient population needs. Evidence-based validation demonstrates improved detection of CNVs—including those smaller than 50 kb—so your results aren’t just comprehensive, they’re actionable.

    By integrating these panels into your existing workflow, you enhance not only the quality of your data but also the efficiency of your lab operations, freeing time and resources for deeper analysis and patient-focused outcomes.

    Select the CNV Resolution You Need

    Select CNV Resolution You Need

    Table 1. Example data of Twist CNV Backbone Spike-in Panels. A highly characterized sample set known to contain CNVs (1) and a baseline set of 12 healthy individuals were sequenced with 2×150 reads on an Illumina NovaSeq 6000. The average number of SNVs, INDELs, and CNVs called and sequencing depth at each probe density was determined for each panel when spiked into Twist Exome 2.0 plus Comprehensive Spike-in. CNV calling was performed with a commercially available software solution (2)
     

    (1) Coriell Institute’s CNVPANEL01 – Human CNV Reference Panel.
    (2) eVai Platform (secondary workflow), enGenome Software. 

    Related Products

    Twist Exome 2.0

    Leading exome solution covering key genetic databases with high uniformity

    Twist Standard Hybridization Reagent Kit

    Reagents for high-efficiency NGS target enrichment (TE).

    Library Preparation Enzymatic Fragmentation Kit 2.0

    Enzymatic DNA fragmentation for efficient library prep.

    Ordering
    Higher Resolution: 

    110756  –  Twist 25kb CNV Backbone Spike-in Panel, 2 Reaction kit

    110757  –  Twist 25kb CNV Backbone Spike-in Panel, 12 Reaction kit

    Intermediate Resolution:

    110758 –  Twist 50kb CNV Backbone Spike-in Panel, 2 Reaction kit

    110759 –  Twist 50kb CNV Backbone Spike-in Panel, 12 Reaction kit

    Lower Resolution: 

    110760 –  Twist 100kb CNV Backbone Spike-in Panel, 2 Reaction kit

    110761 –  Twist 100kb CNV Backbone Spike-in Panel, 12 Reaction kit

    Exome Panels

    104132 –  Twist Exome 2.0, 2 Reactions, Kit

    104134 –  Twist Exome 2.0, 12 Reactions, Kit

    104136 –  Twist Exome 2.0, 96 Reactions, Kit

    105034 –  Twist Exome 2.0 plus Comprehensive Exome Spike-in, 2 Reactions

    105035 –  Twist Exome 2.0 plus Comprehensive Exome Spike-in, 12 Reactions

    105036 –  Twist Exome 2.0 plus Comprehensive Exome Spike-in, 96 Reactions

    *For research use only 

    Chris Wicky

    Clinical Genomics Manager - ANZ
    & Country Manager - NZ

    For guidance on integrating these panels into your operations, Decode Science can provide personalised support and local assistance.
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    A CRE.AI.TIVE application of AI: Engineering a more resilient global food supply

    A CRE.AI.TIVE application of AI: Engineering a more resilient global food supply

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      Phytoform Labs harnessed its AI-powered CRE.AI.TIVE platform to develop climate-resilient crops, with a focus on drought-tolerant tomatoes. By rapidly exploring millions of potential sequence edits, the platform identified 2,000 high-potential candidates for wet-lab validation.

      To overcome the challenge of synthesizing complex, AT-rich sequences with homopolymers, the team partnered with Twist Bioscience. Twist’s high-fidelity oligos ensured accurate transfer of AI-designed sequences to the lab, enabling efficient MPRA screening in tomato protoplasts.

      This AI-guided workflow validated predictions while streamlining experiments—reducing waste, saving resources, and ensuring only the most promising variants progressed to in vivo testing.

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      1. AI-driven design of millions of sequence variants

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      Chris Wicky

      Country Manager - NZ

      As the official distributor in Australia and New Zealand, Decode Science makes accessing genomics solutions straightforward. Our role is to connect your lab with advanced technologies, ensuring you get the right solution for your sequencing projects—delivered locally with support when you need it.

      Site Directed Mutagenesis

      Mutants Synthesized. Mutagenesis Simplified.

      Make Site-Directed Mutagenesis precise, simple, and affordable with Twist’s Mutagenesis by Synthesis. Traditional site-directed mutagenesis can be time consuming and imprecise. Site directed mutagenesis through synthesis eliminates these complexities, providing you with precisely engineered sequences tailored to your exact specifications. From protein engineering to functional genomics, incorporate precision synthesis of mutants into your workflow and focus on achieving your research goals

      Why it matters to you:

      Precision engineering – 

      site-directed mutagenesis, custom DNA

      Flexible design

      protein engineering, functional genomics

      Fast turnaround

      Express Clonal Genes, rapid synthesis

      Cost-effective

      affordable variants, scalable synthesis

      How to Qualify

      Product: Clonal Genes
      Number of mutation per genes: No Limit
      Mutation type: any number of point mutation,
      deletions, and/or insertions*
      Pricing: Discounts on every variant
      (Please kindly contact your Decode Sales Rep for enquiry)

      How it Works

      Terms and Conditions
      * This promo is only available to customers in the Asia Pacific region (excluding China and Japan). Pricing is subjected to changes.
      * To enjoy the special service of site directed mutagenesis, please quote your previous order number or approach Decode Science support.
      * Each mutation is defined as any combination of bases change within a 10 codon spread over the entire gene.
      * Average turnaround time for Express Clonal Genes is 4 -7 business days. This time will vary based on complexity and length of the sequence. Orders placed outside of the US will incur additional delivery turnaround time. Turnaround time for Clonal Genes is subject to change based on customizations and complexity. Additional specification: 50ng – 2 ug.

      Watch Successful Implementations

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      Daina Elliott

      Business Development Manager

      As the authorized distributor of Twist Bioscience in Australia and New Zealand, Decode Science makes integrating Twist’s DNA synthesis solutions seamless. We connect your lab with high-throughput, high-fidelity Twist technology, enabling faster, more reliable genomic workflows—with local support and guidance every step of the way.
      Twist Portfolio
      Twist NGS

      NGS

      Raise confidence in variant detection with superior target enrichment solutions

      Twist Oligo Pools

      Oligo Pools

      Precision, uniformity, and flexibility for results you can trust

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      Synthetic RNA and DNA standards for assay development

      Twist Libraries

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      Twist Antibody

      Antibody

      Robust solutions for Antibody Discovery and Development by Twist Bioscience

      High Throughput Antibody Production

      PRODUCTS

      High Throughput Antibody Production

      Introducing CHO and HEK293 Antibody Production

      Twist Bioscience helps researchers speed up antibody discovery with Express Antibody Production using CHO and HEK293 expression systems. Our high-throughput antibody production platform can generate anywhere from dozens to thousands of antibodies, enabling efficient antibody screening for binding specificity and biophysical properties.

      By leveraging Twist’s end-to-end gene-to-protein workflow, you can eliminate common antibody production bottlenecks—saving valuable time and research costs. Starting with Twist Express Genes ensures faster production times and antibodies built entirely from your custom gene sequences.

      Key Features

      CHO Express Antibodies

      1. From 13 business days*
      2. 1 mL and 8 mL scales available
      3. Average Yields = 640 ug

      HEK293 Express Antibodies

      1. From 10 business days*
      2. 1 mL and 8 mL scales available
      3. Average = Yields 760 ug
      Why Twist for Antibody Production?

      Customization

      Design antibodies with optimal binding affinity, specificity, and reduced immunogenicity.

      Speed & Efficiency

      Rapid, sequence-perfect DNA synthesis accelerates your antibody development timeline.

      Scalable Production

      From small-scale studies to large-scale drug discovery, scale antibody production with ease.

      Cutting-Edge Technology

      Access the latest gene synthesis innovations without high costs.

      Expert Support

      Get 24/7 guidance from antibody design to submission.

      You design it. We build it.
      IgG Workflow - Antibody Production
      What Scientists Have to Say

      Wyatt McDonnell

      CEO & Founding Scientist • Infinnimune

      Using Twist’s solutions saves us hundreds of thousands of dollars annually in labor costs. The cost efficiency of Twist Express Antibodies allows us to test four times as many antibodies each year as we otherwise could.

      Dr. Ahuva Nissim

      Professor in Antibody and Therapeutic Engineering • Queen Mary University of London

      Working with Twist…was a great experience…[Twist’s] support was amazing. We have performed the first validation selections which looks promising…

      Pierre Martineau

      Deputy Director, Cancer Research Institute of Montpellier • Founder and Scientific Advisor, iMAb

      We have performed the first selections using the Fab and scFv libraries. No problem in both cases, we got clones and some look really promising.
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      Know More About...

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        RNA Sequencing

        PRODUCTS

        RNA Sequencing

        RNA Sequencing

        Twist’s RNA sequencing workflows offer a complete NGS solution that produces uniform libraries for RNA sequencing.

        Twist offers targeted and whole transcriptome workflows that reduce time at the bench and integrate with our current set of NGS reagents, including our target enrichment kits. Each workflow delivers high quality libraries ready for sequencing from a wide range of inputs and sample types, including translation research samples.

        RNA Library Prep

        Twist offers two comprehensive RNA sequencing workflows: Targeted RNA Sequencing and Whole Transcriptome Sequencing. The Targeted RNA Sequencing workflow involves creating custom panels to focus on specific RNA transcripts, utilizing streamlined library preparation kits, unique dual indices, molecular identifiers, optimized target enrichment, and a proprietary exon-aware panel design algorithm. This allows for sensitive and efficient sequencing, even with low-quality RNA from FFPE samples.

         

        On the other hand, the Whole Transcriptome Sequencing workflow measures expression levels of various RNA species, including mRNA and lncRNA. It involves preparing libraries from total RNA extracted from both fresh and FFPE samples using Twist RNA Library Prep and Twist rRNA & Globin Depletion kit. This workflow enables RNA Library Preparation in less than 5 hours, providing a comprehensive view of the entire transcriptome. Two charts accompany the descriptions, detailing the targeted and whole transcriptome sequencing workflows.

        RNA Sequencing
        Twist Targeted RNA Sequencing Workflow
        Twist Whole Transcriptome Sequencing Workflow
        More Targets, Fewer Reads
        RNA Exome

        The collaboration of Twist RNA Exome, Twist RNA Library Prep, and Twist Target Enrichment forms a reliable toolkit for transcriptome sequencing, accommodating RNA from diverse sources, including FFPE samples. Notably, the RNA Exome enhances signal strength while requiring fewer sequencing reads, enabling the detection of low-expressing targets crucial for accurate transcriptional profiling. Its exon-aware design approach allows the identification of isoforms and junctions often overlooked in conventional methods, delivering precise and uniform sequencing reads tailored for analyzing protein-coding sequences within the human transcriptome.

         

        Designed exclusively for the human transcriptome, the RNA Exome targets 35.8 Mb bases, 19,708 genes, and 63,215 isoforms using sequences from Gencode and RefSeq. With over a 1.8-fold enrichment compared to whole transcriptome sequencing, it features a target enrichment approach built for RNA, incorporating an exon-aware probe design for protein coding regions, fusions, and isoforms. This design not only ensures precision but also reduces reads per sample, facilitating efficient analysis of multiple samples. The RNA Exome is versatile, compatible with FFPE samples and low RNA input. In practical tests, it demonstrates the capability to detect more targets with fewer reads across a range of RNA inputs, including FFPE and universal human reference RNA, using libraries prepared with the Twist RNA Library Prep.

        RNA Fusion

        The Twist Alliance CeGaT RNA Fusion Panel Kit emerges as a crucial tool in the precise detection of gene fusions, particularly impactful oncogenic driver mutations in various cancer types. Rapid and accurate detection holds significant clinical implications, guiding treatment decisions effectively. This RNA-based enrichment panel stands out by offering an enhanced targeted and sensitive approach, surpassing traditional methods.

         

        Curated in collaboration with CeGaT, a renowned genetic diagnostic and sequencing company in Europe, this panel encompasses 160 fusion genes associated with approximately 30 cancer types. Uniquely, it is designed not only for known gene fusions but also to unveil novel ones. The panel’s efficiency is amplified when used in conjunction with the Twist RNA Library Prep Kit, ensuring an end-to-end workflow with exceptional performance.

         

        With an optimized design featuring 7394 probes and a breakpoint design for 66 genes, the panel excels in covering a diverse array of cancer types. The incorporation of Twist core enrichment technology further maximizes capture efficiency, instilling confidence in RNA gene fusion detection. This panel is particularly well-suited for screening oncology samples, providing critical insights for treatment decisions or uncovering novel fusions for tumor classifications.

         

        *Note: The Twist Alliance CeGaT RNA Fusion Panel – 3 MB holds ISO-13485 certification, reinforcing its reliability in clinical applications.

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          MRD Sequencing

          PRODUCTS

          MRD Sequencing

          MRD Sequencing

          Minimal Residual Disease (MRD), characterized by a small number of lingering malignant cells post-treatment, poses a recurrence risk often undetectable by standard surveillance methods. Twist Bioscience’s MRD Rapid 500 Panel addresses this challenge by utilizing circulating tumor DNA for early detection. Leveraging Twist’s silicon-based DNA synthesis platform, this scalable solution offers rapid turnaround time (as few as 6 business days) with personalized variant profiles from whole-genome or whole-exome sequencing. The MRD panels, featuring 50 to 500 probes, provide comprehensive genomic insights, compatible with Twist’s NGS library preparation and hybrid capture workflow. This facilitates early intervention and enhances personalized medicine approaches in cancer recurrence monitoring.

          Benefits

          Unmatched Scalability and Speed:
          Benefit from unparalleled scalability and efficiency as you capture variants of interest with panels ranging from 50 to 500 probes. Streamline your workflow by ordering up to 150 panels at a time, and experience the rapid shipment of panels within an impressive 6 business days.

          Customized Panel Designs:
          Tailor your panel designs to meet your specific needs using a variant target coordinate BED file. Improve capture performance by strategically filtering probe sequences over repetitive regions, leading to enhanced efficiency and significant cost savings on overall sequencing expenses.

          Panel Information:
          Leverage the advantages of a single plex for 12 tests, ensuring the detection of SNVs and small indels with high precision. Implement quality control through qPCR, and rest assured with ISO-13485 certification, signifying a commitment to reliability. Conveniently receive panels in Matrix Tubes, and benefit from designs supported against hg19 and hg38 reference genomes.

          Lab Workflow:
          Integrate seamlessly into your lab workflow with compatibility with Twist library preparation and hybridization workflows. Follow the recommended hybridization protocol, MRD Standard Hyb 2.0, ensuring not only efficiency but also a streamlined and harmonious laboratory process.

          MRD Rapid 500 Panel Design
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            Long Read Sequencing

            PRODUCTS

            Long Read Sequencing

            Long Read Sequencing

            Combine the precision of Twist target enrichment with the power of long read sequencing to efficiently explore crucial genomic regions at scale. Twist Alliance panels, both pre-designed and customizable, empower researchers to capture target regions in a cost-effective and high-throughput manner, ensuring exceptional performance.

            Exceptional Performance: Elevate your sequencing endeavors with panels specifically crafted for long read sequencing. Probes are optimized for high uniformity and sequencing efficiency, ensuring balanced coverage even across challenging-to-sequence or difficult-to-map genomic regions.

            Long Read Sequencing at Scale: Efficiently scale up your sequencing projects with a protocol optimized for long fragment enrichment. This approach allows you to pack more samples into a single sequencing run, making it possible to study targeted regions across large cohorts.

            Accurate Variant Calling with Targeted HiFi Sequencing from PacBio: Leverage the accuracy of targeted HiFi Sequencing from PacBio for precise variant calling of SNPs, SVs, and indels. Benefit from unambiguous haplotype resolution and long-range phasing, ensuring reliable results. This approach is compatible with Sequel IIe and Revio Systems, providing versatility in sequencing platforms.

            Twist Alliance Dark Genes Panel
            Enables sequencing of genes that are difficult or impossible to fully sequence with short read technology.

            1. Targets 389 genes (20 Mb)
            2. Key targets include GBA, SMN1/2

            Twist Alliance Long-Read PGx Panel
            Focus on important genes in pharmacogenomics that are critical to drug metabolism and patient therapeutic response.

            1. Targets 49 genes (2 Mb)
            2. Key targets include CYP2D6, HLA-A, HLA-B
            Twist Alliance Dark Genes Panel
            Twist Alliance Long-Read PGx Panel
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              Library Preparation

              PRODUCTS

              Library Preparation

              Library Preparation

              Twist Library Preparation Kits offer a streamlined process for constructing high-quality DNA libraries in next-generation sequencing (NGS) applications. Tailored for whole genome sequencing and targeted enrichment, these kits simplify library preparation by combining multiple steps into a single reaction, enhancing efficiency and ensuring consistent results.

              Two configurations are available to cater to different needs: Mechanical Fragmentation, designed for mechanically sheared gDNA, and Enzymatic Fragmentation, ideal for automated, high-throughput library preparation. Both configurations minimize artifacts, accommodate various DNA input types, and optimize sequencing of low-quality samples, with the Enzymatic Fragmentation offering tunable, reproducible fragment sizes while minimizing sequence bias and maximizing coverage depth.

              Library Preparation Workflow

              The Twist Library Preparation Kits provide a comprehensive solution for the entire library preparation workflow, encompassing crucial steps such as end repair, dA-tailing, adapter ligation, and library amplification. Both kits offer versatility in adapter choices, allowing the use of either full-length or universal adapters based on specific application requirements.

              For the Enzymatic Fragmentation Kit, additional functionality includes the incorporation of enzymes for the fragmentation of genomic DNA (gDNA) samples. This feature enhances the kit’s capability for high-throughput library preparation.

              The accompanying chart illustrates a robust library construction process by utilizing Twist Universal Adapters for insert ligation and UDI primer PCR amplification. This approach ensures a streamlined and efficient workflow, producing libraries suitable for a diverse range of applications.

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                Clonal Genes

                PRODUCTS

                Clonal Genes

                Overview

                Twist Bioscience’s advanced platform is designed to meet diverse DNA synthesis needs, with the capability to synthesize hundreds of thousands of genes each month. Utilizing a silicon-based platform for DNA synthesis, Twist delivers highly precise, sequence-perfect clonal genes of various lengths and complexities, all verified through Next-Generation Sequencing (NGS). Now, with the introduction of the Express Genes service, Twist offers even faster turnaround times, synthesising NGS-verified Clonal Genes in as few as 5 days.

                Twist Bioscience’s Express Genes service offers researchers a cost-effective, customizable, and scalable solution for obtaining high-quality clonal genes with efficient turnaround times. This service empowers researchers to accelerate their projects and advance their scientific endeavors with confidence.

                Low Cost – High Quality:

                Priced from 18¢ (AUD) per base pair.

                No hidden sub-cloning or DNA complexity fees.

                Delivery in as fast as 12 business days.

                DNA Your Way:

                Customize 0.3 – 5 kb genes cloned into a plasmid of your choice.

                Choose from Twist Catalog Vectors or provide your own.

                Four preparation scales (50ng – 2µg | 2µg – 10µg | 10µg – 100µg | 100µg – 1mg).

                Options for normalization and endotoxin-free available.

                Scalable Synthesis:

                No order limits, providing flexibility.

                Same turnaround time regardless of order size.

                Express Genes Service

                Introducing Twist Bioscience’s Express Genes service*— synthesising NGS-verified, sequence-perfect Clonal Genes with an unprecedented order-to-ship turnaround time of 5-7 business days. Explore our full Clonal Genes offering below and experience the speed and efficiency of Express Genes for your research needs.

                Genes Table (Clonal and Express Gene)

                *Terms and Conditions: Eligible Express Genes ship in 5-7 business days. This time will vary based on complexity and length of the sequence. Orders placed outside of the US will incur additional delivery turnaround time. Turnaround time for Clonal Genes is subject to change based on customizations and complexity. Average turnaround time for Clonal Genes is 10-15 business days. New vector onboarding for both Express Genes and Clonal Genes will add additional time.

                DATA

                The data presented illustrates the high quality and precision of Twist Bioscience’s Clonal Genes, showcasing a graphical representation of the standard Next-Generation Sequencing (NGS) verification performed on each clonal gene. The featured clonal gene in the figure serves as an example of an error-free clone. The read depth is indicated for the entire plasmid, and no Single Nucleotide Polymorphisms (SNPs) or insertions/deletions (indels) were detected, emphasizing the accuracy and reliability of Twist’s clonal gene synthesis.

                This data emphasizes Twist’s commitment to providing researchers with sequence-perfect clonal genes, ensuring high-quality and error-free results for a wide range of applications in the field of genetic research and synthetic biology.

                Clonal Genes
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                Synbio Genes Portfolio

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                  Gene Fragments

                  PRODUCTS

                  Gene Fragments

                  Overview

                  Twist Bioscience offers Synthetic Gene Fragments as a fast, economical, and efficient solution for building genes in your research. These gene fragments enhance the cloning process by minimizing the need for colony screening, saving valuable time and reducing overall costs associated with cloning and sequencing.

                  By leveraging Twist’s Synthetic Gene Fragments, researchers can think bigger, design on a grander scale, and accelerate their discoveries. With the advantage of an industry-leading error rate, customizable lengths and yields, and the convenience of no order limits, Twist’s Gene Fragments offer a cost-effective and time-efficient solution for diverse research needs. To learn more or place an order, researchers can explore the product sheet or directly proceed with ordering from Twist Bioscience.

                  Fast and Economical:

                  Gene Fragments for assembly and cloning.
                  Compatible with all downstream cloning methods.
                  Priced from 13¢ (AUD) per base pair.
                  Synthesised in as little as 2 business days.

                  Screen Less, Discover More:

                  Industry-leading error rate of 1:7500.
                  Length: 300 bp – 1800 bp.
                  Yield: 100 ng – 1 µg.
                  No order limit.

                  Twist Bioscience’s DNA synthesis technology stands out by outperforming competitors with exceptionally low error rates. In a direct comparison of Gene Fragment products, Twist consistently demonstrated the lowest error rate, as illustrated in the graph comparing Twist and Integrated DNA Technologies, Inc. (IDT). The results reveal that Twist Gene Fragments exhibit greater sequence accuracy compared to eBlocks and gBlocks, boasting an average of 2-fold greater accuracy in sequence fidelity over gBlocks.

                  Moreover, Twist Gene Fragments consistently yield the highest percentage of perfect clones, offering a significant advantage in terms of time and cost savings for researchers. The graph showcasing a direct comparison of the percentage of sequence perfect clones across various gene lengths and sequences for three different gene products highlights Twist’s superiority. The data, derived from a set of 63 sequences with diverse gene lengths, reflects the broad applicability of Twist’s technology in addressing the varied requirements of real-world synthetic biology applications.

                  Gene-Fragments-AverageErrorRate-3
                  perfect-clones-bp-length@2x
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                  SynBio Genes Portfolio

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