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PacBio and International Research Consortium CoLoRS Announce Release of First-Ever HiFi Long-Read Variant Database

PacBio and International Research Consortium CoLoRS Announce Release of First-Ever HiFi Long-Read Variant Database

PacBio和国际研究联盟CoLoRS宣布发布有史以来第一个HiFi长读序列变异数据库

Consortium Delivers Publicly Available Datasets that Enrich Detection of Rare and Novel Genetic Variants for Advances in Human Disease Research

该联盟提供了公开可用的数据集,丰富了检测罕见和新型基因变异体以推进人类疾病研究的进展。

MENLO PARK, Calif., June 10, 2024 /PRNewswire/ -- PacBio (NASDAQ: PACB), a leading developer of high-quality, highly accurate sequencing solutions, in collaboration with the international Consortium for Long-Read Sequencing (CoLoRS), today announced the launch of the first publicly available and free HiFi long-read variant frequency database with global representation. This innovative resource fills a critical void for rare disease researchers, providing access to genetic variants that are not detectable through short-read sequencing methods. By enabling the filtering of common structural variants from long-read sequencing data, this database allows for the identification of rare and novel variants in rare disease cases. The launch of this database better enables researchers to utilize long-read genomic data to advance human health research.

加州门洛帕克,2024年6月10日/美通社/-- PacBio (NASDAQ:PACB)是一家领先的高质量、高精度测序解决方案的开发者,与国际长读序列联盟(CoLoRS)合作,宣布推出首个具有全球代表性的及免费的HiFi长读异类频率数据库。这个创新资源填补了罕见疾病研究者的关键空白,提供了无法通过短读测序方法检测到的基因变异体的访问。通过启用长读序列数据中的常见结构变异体过滤,该数据库允许在罕见病例中识别罕见和新的变异体。推出这个数据库更好地使研究人员利用长读基因组数据推进人类健康研究。

"Joining forces with PacBio has enabled us to leverage their HiFi sequencing capabilities, enhancing the depth and accuracy of the genomic data we can offer to the research community," said Michael Schatz, Bloomberg Distinguished Professor at Johns Hopkins University. "This effort complements existing databases such as gnomAD, as long reads enable much greater sensitivity and precision for complex variants (SVs) and tandem repeats. The CoLoRS database is a tremendous step forward in our collective effort to understand complex genetic variations and their implications in disease."

“加入PacBio使我们能够利用他们的HiFi测序能力,提高我们可以提供给研究社区的基因组数据的深度和准确性,”约翰斯·霍普金斯大学的彭博杰出教授迈克尔·沙兹说。“这一努力补充了gnomAD等现有数据库,长读测序使复杂变异体和串联重复的灵敏度和精确性远高于短读。CoLoRS数据库是我们共同努力理解复杂遗传变异及其在疾病中的影响的重要一步。”

Studies have shown that long-read sequencing finds 15,000 more structural variants (SVs) and 300,000 more small variants than short reads. SVs are crucial as they account for much of the genetic diversity between humans and are associated with disease pathogenesis. The CoLoRS database integrates data from nearly 1,000 long-read genomes, providing detailed insights into human variation and improving the detection of complex variants and tandem repeats. This resource is developed by a global coalition from top clinical and academic institutions, pooling diverse long-read genome data from various research projects.

研究表明,长读测序发现了15,000多个结构变异体(SVs)和300,000个小变异体,比短读多出很多。结构变异体(SVs)是至关重要的,因为它们占人类之间的大部分遗传多样性,并与疾病发病机制有关。CoLoRS数据库整合了近1,000个长读基因组的数据,提供了有关人类变异的详细见解,改善了复杂变异体和串联重复的检测。这个资源由来自顶级临床和学术机构的全球联盟组成,共同整合了来自各种研究项目的不同类型的长读基因组数据。

"We are thrilled to see the launch of the CoLoRS database, a pivotal development in genomics research," said Christian Henry, President, and Chief Executive Officer of PacBio. "This collaboration with the CoLoRS members exemplifies our commitment to supporting the scientific community with tools that enhance the accuracy and utility of genetic research. It also demonstrates the unique capabilities of our HiFi sequencing technology. By making this information accessible to the public, we are empowering researchers around the world to make significant advances in areas such as oncology, rare diseases, and genetic disorders."

“我们非常高兴看到CoLoRS数据库的推出,这是基因组研究的一个关键发展,” PacBio的总裁兼首席执行官克里斯蒂安·亨利说。“与ColoRS成员的合作体现了我们支持科学界用工具提高遗传研究的准确性和实用性的承诺。它还展示了我们的HiFi测序技术的独特能力。通过向公众提供这一信息,我们正在授权全世界的研究人员在肿瘤学、罕见病和遗传性疾病等领域取得重大进展。”

Researchers are invited to access the CoLoRS database and explore its capabilities at www.colorsdb.org. Supported by PacBio's HiFi sequencing technology, this platform provides researchers with new insights into human genomic variation, accelerating advancements in critical areas of medical research.

欢迎访问CoLoRS数据库,了解其功能,请访问www.colorsdb.org。由PacBio的HiFi测序技术支持,该平台为研究人员提供了对人类基因组变异的新洞察,加速了医疗研究的重要领域的进展。www.colorsdb.org。支持PacBio的HiFi测序技术,该平台为研究人员提供了对人类基因组变异的新洞察,加速了医疗研究的重要领域的进展。

About PacBio
PacBio (NASDAQ: PACB) is a premier life science technology company that designs, develops, and manufactures advanced sequencing solutions to help scientists and clinical researchers resolve genetically complex problems. Our products and technologies stem from two highly differentiated core technologies focused on accuracy, quality and completeness which include our HiFi long-read sequencing and our SBB short-read sequencing technologies. Our products address solutions across a broad set of research applications including human germline sequencing, plant and animal sciences, infectious disease and microbiology, oncology, and other emerging applications. For more information, please visit www.pacb.com and follow @PacBio.

关于PacBio
PacBio(纳斯达克:PACB)是一家高端生命科学技术公司,设计、开发和制造先进的测序解决方案,以帮助科学家和临床研究人员解决基因复杂问题。我们的产品和技术源于两个高度差异化的核心技术,专注于精度、质量和完整性,包括我们的HiFi长读序列和我们的SBB短读序列技术。我们的产品涵盖了广泛的研究应用,包括人类生殖系测序、植物和动物科学、传染病和微生物学、肿瘤学和其他新兴应用。欲了解更多信息,请访问www.pacb.com,并关注@PacBio。www.pacb.com并关注@PacBio。

PacBio products are provided for Research Use Only. Not for use in diagnostic procedures.

PacBio产品仅供研究使用。不适用于诊断程序。

Forward-Looking Statements
This press release may contain "forward-looking statements" within the meaning of Section 21E of the Securities Exchange Act of 1934, as amended, and the U.S. Private Securities Litigation Reform Act of 1995. All statements other than statements of historical fact are forward-looking statements, including statements relating to the uses, coverage, advantages, quality or performance of, or benefits or expected benefits of using, PacBio products or technologies; enabling researchers to utilize long-read genomic data to advance human health research; empowering researchers to make significant advances in areas such as oncology, rare diseases, and genetic disorders; and other future events. You should not place undue reliance on forward-looking statements because they are subject to assumptions, risks, and uncertainties and could cause actual outcomes and results to differ materially from currently anticipated results, including, challenges inherent in sequencing a large number of whole human genomes, and the difficulty of generating discoveries across various areas of research; unanticipated increases in costs or expenses; interruptions or delays in the supply of components or materials for, or manufacturing of, PacBio products and products under development; potential product performance and quality issues; third-party claims alleging infringement of patents and proprietary rights or seeking to invalidate PacBio's patents or proprietary rights; and other risks associated with international operations. Additional factors that could materially affect actual results can be found in PacBio's most recent filings with the Securities and Exchange Commission, including PacBio's most recent reports on Forms 8-K, 10-K, and 10-Q, and include those listed under the caption "Risk Factors." These forward-looking statements are based on current expectations and speak only as of the date hereof; except as required by law, PacBio disclaims any obligation to revise or update these forward-looking statements to reflect events or circumstances in the future, even if new information becomes available.

前瞻性声明
本新闻稿可能包含《证券交易法》修正案第21E条和1995年美国私人证券诉讼改革法案中的“前瞻性声明”。除历史事实陈述外,所有陈述均属于前瞻性声明,包括与使用PacBio产品或技术,覆盖范围、优势、质量或性能,或使用PacBio产品或技术的预期或预期的好处;使研究人员利用长读基因组数据推进人类健康研究;使全球研究人员能够在肿瘤学、罕见病和遗传性疾病等领域取得重大进展;以及其他未来事件。您不应该过度依赖前瞻性声明,因为它们受到假设、风险和不确定性的影响,可能导致当前预期的结果和结果与实际结果不符,包括关于使用各种研究领域的大量整个人类基因组的技术的挑战,以及在各种研究项目中涉及的难以发现的问题;成本或费用的意外增加;为PacBio产品和正在开发中的产品供应元件或材料的中断或延迟;潜在的产品性能和质量问题;第三方声称侵犯专利和专有权或试图使PacBio的专利或专有权无效的权利和其他与国际业务有关的风险。这些前瞻性声明基于当前预期,仅截至此日期;除法律要求外,PacBio不承担修订或更新这些前瞻性声明以反映未来事件或情况的任何义务,即使有新信息可用也是如此。

Contacts
Investors:
Todd Friedman
ir@pacificbiosciences.com

联系方式
投资者:
Todd Friedman
ir@pacificbiosciences.com

SOURCE Pacific Biosciences of California, Inc.

资讯来源:pacific biosciences of california

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