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Press Alt+1 for screen-reader mode, Alt+0 to cancelAccessibility Screen-Reader Guide, Feedback, and Issue Reporting Menu * Products * Sequencing systems * Revio long-read system * Vega benchtop system * Onso short-read system * Sequel long-read systems * Technologies * HiFi long-read sequencing * SBB short-read sequencing * Kinnex * PureTarget * Nanobind DNA extraction * Consumables * Sample prep * Application kits * Library prep + barcoding * HiFi sequencing * Onso sequencing * Sequencing methods * Whole genome sequencing * Human * Plant + animal * Microbiology + infectious disease * Variant detection * Targeted sequencing * RNA sequencing * Single-cell RNA sequencing * Epigenetics * Microbiome + metagenomics * Software + bioinformatics * SMRT Link * Computational tools * Onso software * Compatible partner software * Purchase * Ask a question * Request pricing * PacBio Capital * Customer hub * Global distributors * Compatible products * Certified service providers * Focus areas * Human genomics * Genetic testing * Clinical research * Rare disease * Repeat expansions * Pop Gen * HiFi Solves * Human research * Neurogenomics * Immunogenomics * Microbial genomics * Public health + surveillance * HiFiViral COVID-19 surveillance * Infectious disease research * Microbial sequencing methods * Plant + animal microbes * Plant + animal genomics * Agrigenomics * Biodiversity * Plant + animal biology * Plant + animal hub * Cancer genomics * Liquid biopsy * Biopharma * Gene therapy * Gene editing * Biologics R&D * Engage * Connect * Become a sequencing service provider * Find certified service providers * Find distributors * Apply for grants * Access datasets * Learn * Blog * Webinars * Case studies * Free resources * Scientific publications * Posters * Literature * Educational videos * Sequencing 101 * HiFi Difference * Events * Past events * Support * Documentation * Technical support * Support FAQs * Training * HiFi software downloads * Onso software downloads * Protocols * Multiplexing * Company * About us * Leadership * Board of Directors * Scientific Advisory Board * Careers * FAQs * Benefits * Culture * Equal employment opportunity * News * Press releases * Events * Investors * Sustainability * Legal * Privacy * Terms * Additional Product-Specific Terms and Conditions * Products * Software * Other * Warranty * Images * Privacy policy * Contact * 日本語 * 全ゲノムシーケンス * ターゲットシーケンス * ISO-SEQによるRNAシーケンス * エピジェネティクス * メタゲノミクス * 中文 * Customer hub Skip to content Home * Products * Sequencing systems * Revio long-read system * Vega benchtop system * Onso short-read system * Sequel long-read systems * Technologies * HiFi long-read sequencing * SBB short-read sequencing * Kinnex * PureTarget * Nanobind DNA extraction * Consumables * Sample prep * Application kits * Library prep + barcoding * HiFi sequencing * Onso sequencing * Sequencing methods * Whole genome sequencing * Targeted sequencing * RNA sequencing * Epigenetics * Microbiome + metagenomics * Software + bioinformatics * SMRT Link * Computational tools * Onso software * Compatible partner software * Purchase * Ask a question * Request pricing * PacBio Capital financing * Customer hub * Global distributors * Compatible products * Certified service providers * Focus areas * Human genomics * Genetic testing * Clinical research * Rare disease * Repeat expansions * Population genomics * HiFi Solves * Human research * Neurogenomics * Immunogenomics * Microbial genomics * Public health + surveillance * Infectious disease research * Microbial sequencing methods * Plant + animal microbes * Plant + animal genomics * Agrigenomics * Biodiversity * Plant + animal biology * Plant + animal hub * Cancer genomics * Liquid biopsy * Biopharma * Gene therapy * Gene editing * Biologics R&D * Engage * Connect * Become a sequencing service provider * Find certified service providers * Find distributors * Apply for grants * Access datasets * Learn * Blog * Webinars * Case studies * Resources * Scientific publications * Posters * Literature * Educational videos * Sequencing 101 * HiFi Difference * Events * Past events ALS CASE STUDY See how the University of Washington used HiFi sequencing to uncover a key finding about ALS and the human genome. View case study * Support SUPPORT We have assembled an experienced team of technical support scientists, engineers, and bioformaticians to assist you with all of your support needs. Email us Monday–Friday 7 AM – 5 PM PST 1.877.920.PACB (7222) Visit customer hub * Documentation * Technical support * Support FAQs * Training * HiFi software downloads * Onso software downloads * Protocols * Multiplexing * Certifications * Company * About us * Leadership * Board of Directors * Scientific Advisory Board * Careers * Press releases * Media resources * News * Events * Investors * Legal * Privacy policy * Sustainability * Contact * * Toggle * English * -------------------------------------------------------------------------------- * 日本語 * 中文 * Visit customer hub * Home * Products * Focus areas * Engage * Support * Company * Contact * 日本語 * 中文 * Customer hub * Contact * * Toggle * English * -------------------------------------------------------------------------------- * 日本語 * 中文 SEQUENCING 101 Follow along to learn more about our technology, reveal the impacts of long-read sequencing, and uncover tips on how to get started. Featured article SEQUENCING 101: LONG-READ SEQUENCING Long-read sequencing technologies are quickly becoming the new gold standard in genomics research, and HiFi sequencing is at the forefront. This article provides an introductory look at what long-read sequencing is, and explores topics the advantages, applications of using long-read sequencing in your research. Read more What are genomic variants and why do they matter? The genetic blueprint of every living organism, from humans to microbes, is written in DNA. This blueprint is shaped by a remarkable phenomenon: genetic variation. These variations, or differences… Learn more Sequencing 101: Comparing long-read sequencing technologies In the rapidly advancing field of genomics, choosing the right long-read sequencing technology is key to meeting your experimental goals smoothly and successfully. To make an informed decision,… Learn more Sequencing 101: Metagenome-assembled genomes Microorganisms form the foundations of life on Earth. They shaped our planet long before we were here, and continue to shape our environments and our lives. Understanding microbial… Learn more Sequencing 101: Structural variation Over the last 50 years, many monumental achievements in genetics and biology have unfolded before our eyes. From the invention of DNA sequencing technologies to the completion of the human… Learn more Sequencing 101: Tandem repeats In the field of genetics, the concept of tandem repeats has been both scientifically fascinating, experimentally challenging, and motivating for technology development. As DNA sequencing technologies and analysis tools have… Learn more Sequencing 101: SBB sequencing Since the inception of next generation sequencing (NGS) more than a decade ago, short-read sequencing accuracy has seen only marginal improvement. Having achieved a level of precision thought to be… Learn more Sequencing 101: The SMRT Cell in PacBio long-read sequencing If you have ever clicked around the PacBio website or attended a workshop or webinar discussing PacBio long-read sequencing technology, then you have probably seen or heard about SMRT (Single… Learn more Sequencing 101: Sequencing coverage This article explores sequencing coverage fundamentals. Uncover key concepts and discover how highly accurate long-read sequencing provides a comprehensive view of the genome, at any coverage level. What is sequencing… Learn more Sequencing 101: How does whole genome sequencing help us understand rare diseases? Updated on March 2, 2023 Rare diseases are defined as diseases that affect a small number of people — fewer than 1 in 2,000 in the European Union and… Learn more 123>> TALK WITH AN EXPERT If you have a question, need to check the status of an order, or are interested in purchasing an instrument, we're here to help. Home Our revolutionary sequencing technologies combine the completeness of long reads with the accuracy of short reads to provide the most comprehensive view of genomes, transcriptomes, and epigenomes. * Connect with us * Linkedin icon New Window * * PRODUCTS * * Technologies * Sequencing systems * Sequencing methods * Consumables * Compatible products * Software + bioinformatics * Purchase * Documentation FOCUS AREAS * * Human genomics * Plant + animal * Infectious disease * Microbial genomics * Cancer research * Biopharma ENGAGE * * Blog * Webinars * Events * Case studies * Sequencing 101 * Access datasets * Resources * Become a service provider * Find a service provider * Find a distributor COMPANY * * About us * Contact us * Leadership * Press releases * Investors * Sustainability * Careers * Support * Customer hub © 2024 PacBio. All rights reserved. Research use only. Not for use in diagnostic procedures. 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