Business terms in the field Flashcards

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OEM or “OEM’ing”

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OEM stands for Original Equipment Manufacturer. It is a term used in the manufacturing industry to describe companies that produce components or products that are sold to other companies to be integrated into their own products.

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Q

What are some products/companies that Twist has OEM’s with?

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Illumina: Twist and Illumina co-developed the Twist Bioscience for Illumina Exome 2.0 Plus panel, designed for use on Illumina sequencers. Twist manufactures this panel, which incorporates an updated set of protein-coding content, disease-associated, and non-coding variants relevant to research applications.
TWIST BIOSCIENCE INVESTORS

GenapSys: In partnership with GenapSys, Twist provides a comprehensive range of target enrichment and library preparation tools for NGS. This collaboration enables GenapSys customers to access optimized assays, including cancer test panels and whole human exome sequencing.
TWIST BIOSCIENCE INVESTORS

Berry Genomics: Twist collaborates with Berry Genomics to offer NGS target enrichment and library preparation tools in China. This partnership combines Berry Genomics’ sequencing expertise with Twist’s manufacturing capabilities to deliver assays for cancer diagnosis and genetic disease research.
PRESS RELEASE SERVICES

Watchmaker Genomics: Twist and Watchmaker Genomics have partnered to enhance high-throughput NGS applications. Their collaboration focuses on oncology, tumor profiling, inherited disease detection, liquid biopsy assays, and minimal residual disease monitoring.

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Q

NGS

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Next-Generation Sequencing (NGS)
Definition: A high-throughput method used to sequence DNA and RNA, enabling rapid and comprehensive genomic analysis. Key technologies include Illumina, PacBio, and Oxford Nanopore.

Why it’s important: Understanding NGS is foundational to your role. You’ll be discussing various sequencing platforms and their applications.

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4
Q

Target Enrichment

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  1. Target Enrichment
    Definition: A method used to selectively capture and sequence specific regions of the genome, such as exons, genes, or cancer-related mutations.

Why it’s important: Twist offers high-quality target enrichment products for a variety of applications. Familiarize yourself with these offerings.

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5
Q

Custom panels

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Custom Panels
Definition: Panels that are specifically designed to target particular genes, mutations, or pathways based on a customer’s unique needs, often used in clinical or research settings.

Why it’s important: Custom panels are a big selling point for Twist’s customers, allowing them to tailor their sequencing efforts to specific targets.

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6
Q

Bioinformatics

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  1. Bioinformatics
    Definition: The use of software and algorithms to interpret and analyze the large data sets generated by NGS.

Why it’s important: Understanding bioinformatics solutions or partnerships related to Twist’s products (e.g., data analysis pipelines) can help you support customers using NGS data.

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7
Q

Gene Editing

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Gene Editing
Definition: A molecular biology method used to alter the DNA of an organism. CRISPR-Cas9 is one of the most popular gene-editing tools.

Why it’s important: Twist offers products related to gene editing, and being familiar with this area helps position Twist’s products in research related to gene modification.

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8
Q

Library Prep

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Library Preparation
Definition: The process of preparing DNA or RNA samples for sequencing by adding specific adapters and preparing the sequenceable fragments.

Why it’s important: Twist provides high-quality library preparation products. You’ll need to explain their benefits to customers.

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9
Q

OEM

A
  1. OEM (Original Equipment Manufacturer)
    Definition: A company that manufactures products or components that are used in another company’s final product.

Why it’s important: Twist collaborates with OEM partners to provide sequencing solutions. Familiarize yourself with these partnerships to better support customers using these solutions.

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10
Q

TAT

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Turnaround Time (TAT)
Definition: The amount of time it takes to complete a service or product from start to finish.

Why it’s important: Customers often prioritize TAT, especially in clinical and diagnostics applications. Understanding this can help you set realistic expectations.

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11
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Accuracy and Precision

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Accuracy and Precision
Definition: Accuracy refers to how close a measurement is to the true value, and precision refers to how consistent results are across repetitions.

Why it’s important: NGS customers care deeply about the accuracy and precision of their sequencing results. You’ll need to discuss how Twist’s products deliver high-quality data.

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Q

Regulatory Compliance

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Regulatory Compliance (e.g., CLIA, FDA)
Definition: Regulations that govern medical devices, diagnostic tests, and laboratory processes in certain markets (e.g., CLIA for laboratories, FDA for devices).

Why it’s important: Many customers in the clinical space will require compliance with these standards. Twist’s products may need to meet these requirements, and you’ll need to explain this.

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13
Q

BED files

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BED files are a standard file format used to describe genomic regions. They are typically used to represent data related to targeted sequencing, genomic intervals, or regions of interest in a genome, such as exons, genes, or specific mutations. The name “BED” comes from the term “Browser Extensible Data,” and these files are often used in genome browsers like UCSC Genome Browser to visualize specific regions of a genome.
In summary, BED files are a vital part of NGS data analysis and are used to define and manage regions of interest in genomic studies, such as targeted sequencing, variant analysis, and visualization.

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14
Q

WGS

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Whole Genome Sequencing (WGS)
What it is: Sequencing of the entire genome, including all coding and non-coding regions.

Why it’s important: Scientists may ask about Twist’s ability to support WGS applications for comprehensive genetic analysis.

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15
Q

WES

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Whole Exome Sequencing (WES)
What it is: A technique that sequences only the protein-coding regions of the genome (the exome).

Why it’s important: WES is widely used in disease research and genetic diagnostics. Twist offers exome capture kits, and scientists may ask how Twist’s products compare to others in this area.

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16
Q

Reads and Read Length

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Reads and Read Length
What it is: A “read” is a sequence of DNA fragments generated during NGS. Read length refers to the number of bases sequenced per read.

Why it’s important: Scientists might ask about the quality of Twist’s sequencing products and whether they can support long-read sequencing or short-read applications.

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Q

Library Prep

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What it is: The process of converting DNA or RNA samples into a format suitable for sequencing by adding adapters and primers.

Why it’s important: Library preparation is crucial for sequencing accuracy. Scientists will want to know if Twist offers high-quality, efficient library prep kits for specific types of samples (e.g., FFPE, cfDNA).

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Q

PCR and qPCR

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What it is: PCR is used to amplify specific DNA sequences, and quantitative PCR (qPCR) quantifies DNA in real time.

Why it’s important: Many NGS applications require PCR to enrich target regions. Researchers may ask about the compatibility of Twist products with PCR-based enrichment methods.

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Q

Variant Calling

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Variant Calling
What it is: The process of identifying variations (e.g., SNPs, indels) in the sequenced data compared to a reference genome.

Why it’s important: Scientists will want to ensure that Twist’s products can be used in accurate variant detection, especially in clinical or diagnostic settings.

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Q

Depth of Coverage

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Coverage
What it is: The number of times a specific genomic region is sequenced, affecting the accuracy of variant detection.

Why it’s important: Customers will ask about the coverage uniformity and how Twist’s products ensure high-depth coverage for sensitive applications like rare variant discovery.

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Q

High Throughput Seq

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High Throughput Sequencing (HTS)
What it is: The ability to sequence large amounts of DNA in parallel, providing massive amounts of data in a short period.

Why it’s important: You’ll be selling products that enable HTS. Scientists might inquire about how Twist’s technology supports scalability for large-scale projects.

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Q

Methylation Seq

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Methylation Sequencing
What it is: A sequencing technique that identifies DNA methylation patterns, which play a role in gene expression regulation.

Why it’s important: Twist offers products for targeted methylation sequencing. Scientists working on epigenetics might ask about the accuracy and coverage for methylation profiling.

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Q

RNA Seq

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RNA-Seq
What it is: A sequencing method used to examine the transcriptome, identifying and quantifying RNA molecules in a sample.

Why it’s important: Scientists involved in gene expression or transcriptomics may inquire about Twist’s offerings for RNA-Seq, including library prep kits and target enrichment.

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Q

WTS

A

. Whole Transcriptome Sequencing (WTS)
What it is: Sequencing of all RNA molecules in a sample, which includes mRNA and non-coding RNAs.

Why it’s important: Similar to RNA-Seq, WTS is used for comprehensive transcript analysis. Researchers may ask if Twist can provide solutions for this broad application.

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Mutational landscape
What it is: The complete set of mutations found in a particular cancer, disease, or genome. Why it’s important: Researchers, especially in oncology, will want to know how Twist’s products can be used to analyze mutational landscapes and identify biomarkers.
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Multi-omics
Multi-Omics What it is: Integrating different types of biological data, such as genomics, transcriptomics, proteomics, and metabolomics. Why it’s important: Scientists might be working on multi-omics projects and will ask how Twist’s products can integrate with other technologies to analyze complex data sets.
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Liquid Biopsy
What it is: A non-invasive method of detecting cancer-related mutations and other biomarkers from blood or other bodily fluids. Why it’s important: Twist has products that support liquid biopsy applications. Customers may ask about Twist's capability for cfDNA or ctDNA sequencing.
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Automation and high throughput Seq
Automation and High-Throughput Systems What it is: The use of automated systems to speed up sequencing processes and increase throughput. Why it’s important: Customers using NGS platforms in large-scale labs will be interested in whether Twist’s products can integrate into automated workflows.
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Automation in NGS
Key Components of Automation in NGS: Sample Preparation Automation: Involves automating the extraction of DNA/RNA, library preparation, and quality control processes. Example: Automated liquid handling systems for preparing NGS libraries. High-Throughput Sequencing Platforms: Many sequencing platforms, such as Illumina and PacBio, are already automated to handle large volumes of sequencing runs with minimal manual intervention. Data Analysis and Interpretation: Software platforms and pipelines can automate the analysis of sequencing data, including quality control, alignment, variant calling, and annotation. Example: Using bioinformatics pipelines that automatically process sequencing data and produce reports. Liquid Handling Systems: Automated liquid handlers can perform precise pipetting tasks for library preparation or sample pooling, increasing consistency and throughput. Next-Generation Data Storage and Management: Automation in managing large datasets from sequencing by storing, indexing, and accessing genomic data more efficiently.
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Names of automation devices and the companies that sell them
1. Thermo Fisher Scientific Automation Products: KingFisher™ Flex System: An automated liquid handling system used for nucleic acid extraction and sample preparation. Ion Chef™ System: For automated library preparation and template preparation for Ion Torrent sequencing platforms. MagMAX™ Kits: Integrated with automated systems for DNA, RNA, and protein extraction. Why it’s relevant: Thermo Fisher provides a comprehensive range of automation solutions, from sample extraction to library prep and sequencing. 2. Illumina Automation Products: Illumina Automation Solutions: These include integration with liquid handling robots for library preparation, DNA extraction, and other sample prep tasks. Illumina® NeoPrep™ System: A streamlined system for automated NGS library preparation, compatible with various Illumina sequencers. NextSeq™ and NovaSeq™ Systems: These sequencing platforms are highly automated and designed for high-throughput sequencing. Why it’s relevant: Illumina is one of the largest NGS platform providers and offers solutions that integrate with automation systems for large-scale sequencing projects. 3. Beckman Coulter Life Sciences Automation Products: Biomek™ Series: Automated liquid handling systems, including the Biomek i7 and i5, which are used for NGS sample preparation and other laboratory processes. Genomic DNA Extraction Automation: Automation of DNA extraction for various applications, including NGS. DNA & RNA Sample Prep Solutions: Customizable protocols for high-throughput sample preparation. Why it’s relevant: Beckman Coulter’s Biomek systems are widely used in labs for automating sample handling, including NGS workflows. 4. Hamilton Company Automation Products: Microlab™ STAR: Liquid handling robots designed for high-throughput applications, including NGS library prep. Verso™ Workstation: Automated systems for extracting and preparing samples, especially in genomics. Customizable Workstations: Hamilton offers flexible automation systems that can be tailored to specific NGS workflows. Why it’s relevant: Hamilton is well-known for its liquid handling automation solutions, which integrate with NGS platforms for precise and reproducible sample prep. 5. Agilent Technologies Automation Products: Bravo™ Automated Liquid Handling Platform: High-throughput, flexible liquid handling systems ideal for NGS library preparation and sample processing. SureSelect™ Target Enrichment: Agilent offers automated solutions for target enrichment (e.g., hybrid capture), which are often used in NGS for focused sequencing applications. Why it’s relevant: Agilent provides integrated systems for both the preparation and enrichment phases of NGS workflows. 6. QIAGEN Automation Products: QIAGEN® GeneReader™ Platform: A fully integrated, automated NGS solution designed for high-throughput sequencing and clinical applications. QIACube™ and QIAgility™: Liquid handling systems that automate sample preparation for genomic analysis, including NGS workflows. Why it’s relevant: QIAGEN is a major player in molecular biology with automated solutions tailored to genomic sample preparation and sequencing workflows. 7. Eppendorf Automation Products: epMotion™ 5070: A liquid handling robot used for automating tasks like NGS library preparation, PCR setup, and other genomic workflows. epT.I.P.S.®: High-quality tips for accurate pipetting, which can be used with automation systems for precise sample preparation. Why it’s relevant: Eppendorf’s products are widely used in research labs to automate repetitive and time-consuming tasks, such as NGS sample prep. 8. Labcorp Drug Development Automation Products: Automated Genomic Services: Labcorp offers comprehensive genomic services, including NGS sample prep automation for clinical trials. Why it’s relevant: Labcorp provides tailored automation solutions for clinical applications, particularly for high-throughput NGS testing in drug development and diagnostics. 9. PerkinElmer Automation Products: Sciclone™ ALH 3000 and 4000: Automated liquid handling systems used for NGS workflows, including nucleic acid extraction and library prep. Chemagic™ Systems: Integrated automation platforms designed for genomic analysis, including automated DNA/RNA extraction for NGS. Why it’s relevant: PerkinElmer specializes in automated systems for molecular biology workflows, including NGS applications. 10. Becton Dickinson (BD) Automation Products: BD FACSAria™ Fusion Cell Sorter: While primarily for cell sorting, it’s often integrated into NGS workflows that involve single-cell analysis or sorting of specific cell populations. Why it’s relevant: BD’s automation systems are particularly useful for integrating NGS with single-cell genomics and other advanced sequencing applications. 11. Roboz (part of Hain Lifescience) Automation Products: Roboz offers various liquid handling and automation systems that integrate with NGS workflows for libraries, PCR reactions, and sample extraction. Why it’s relevant: Roboz’s automation solutions can be applied to streamline preparation for clinical NGS and microbiological studies.
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When would a customer bring up automation?
Scaling Up: When they need to process a large volume of samples (e.g., for clinical diagnostic labs or large research projects). Consistency: When aiming to reduce human error and ensure reproducible results across multiple samples or sequencing runs. Time Efficiency: To accelerate sample processing times and reduce bottlenecks in workflows, especially in high-throughput environments. Integration with Existing Systems: Customers may inquire about how Twist Bioscience’s NGS products can be integrated into their current automated systems for library prep, sequencing, and data analysis. Clinical or Commercial Use: For labs that need to meet high standards of reproducibility, compliance, and turnaround times, automation is critical.
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