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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和國際研究聯盟CoLoRS宣佈發佈有史以來第一個HiFi長讀序列變異數據庫

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

該聯盟提供了公開可用的數據集,豐富了檢測罕見和新型基因變異體以推進人類疾病研究的進展。

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.

加州門洛帕克,2024年6月10日/美通社/-- PacBio (NASDAQ:PACB)是一家領先的高質量、高精度測序解決方案的開發者,與國際長讀序列聯盟(CoLoRS)合作,宣佈推出首個具有全球代表性的及免費的HiFi長讀異類頻率數據庫。這個創新資源填補了罕見疾病研究者的關鍵空白,提供了無法通過短讀測序方法檢測到的基因變異體的訪問。通過啓用長讀序列數據中的常見結構變異體過濾,該數據庫允許在罕見病例中識別罕見和新的變異體。推出這個數據庫更好地使研究人員利用長讀基因組數據推進人類健康研究。

"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使我們能夠利用他們的HiFi測序能力,提高我們可以提供給研究社區的基因組數據的深度和準確性,”約翰斯·霍普金斯大學的彭博傑出教授邁克爾·沙茲說。“這一努力補充了gnomAD等現有數據庫,長讀測序使複雜變異體和串聯重複的靈敏度和精確性遠高於短讀。CoLoRS數據庫是我們共同努力理解複雜遺傳變異及其在疾病中的影響的重要一步。”

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,長讀測序發現了15,000多個結構變異體(SVs)和300,000個小變異體,比短讀多出很多。結構變異體(SVs)是至關重要的,因爲它們占人類之間的大部分遺傳多樣性,並與疾病發病機制有關。CoLoRS數據庫整合了近1,000個長讀基因組的數據,提供了有關人類變異的詳細見解,改善了複雜變異體和串聯重複的檢測。這個資源由來自頂級臨床和學術機構的全球聯盟組成,共同整合了來自各種研究項目的不同類型的長讀基因組數據。

"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."

“我們非常高興看到CoLoRS數據庫的推出,這是基因組研究的一個關鍵發展,” PacBio的總裁兼首席執行官克里斯蒂安·亨利說。“與ColoRS成員的合作體現了我們支持科學界用工具提高遺傳研究的準確性和實用性的承諾。它還展示了我們的HiFi測序技術的獨特能力。通過向公衆提供這一信息,我們正在授權全世界的研究人員在腫瘤學、罕見病和遺傳性疾病等領域取得重大進展。”

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.

歡迎訪問CoLoRS數據庫,了解其功能,請訪問www.colorsdb.org。由PacBio的HiFi測序技術支持,該平台爲研究人員提供了對人類基因組變異的新洞察,加速了醫療研究的重要領域的進展。www.colorsdb.org。支持PacBio的HiFi測序技術,該平台爲研究人員提供了對人類基因組變異的新洞察,加速了醫療研究的重要領域的進展。

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.

關於PacBio
PacBio(納斯達克:PACB)是一家高端生命科學技術公司,設計、開發和製造先進的測序解決方案,以幫助科學家和臨床研究人員解決基因複雜問題。我們的產品和技術源於兩個高度差異化的核心技術,專注於精度、質量和完整性,包括我們的HiFi長讀序列和我們的SBB短讀序列技術。我們的產品涵蓋了廣泛的研究應用,包括人類生殖系測序、植物和動物科學、傳染病和微生物學、腫瘤學和其他新興應用。欲了解更多信息,請訪問www.pacb.com,並關注@PacBio。www.pacb.com並關注@PacBio。

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

PacBio產品僅供研究使用。不適用於診斷程序。

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.

前瞻性聲明
本新聞稿可能包含《證券交易法》修正案第21E條和1995年美國私人證券訴訟改革法案中的“前瞻性聲明”。除歷史事實陳述外,所有陳述均屬於前瞻性聲明,包括與使用PacBio產品或技術,覆蓋範圍、優勢、質量或性能,或使用PacBio產品或技術的預期或預期的好處;使研究人員利用長讀基因組數據推進人類健康研究;使全球研究人員能夠在腫瘤學、罕見病和遺傳性疾病等領域取得重大進展;以及其他未來事件。您不應該過度依賴前瞻性聲明,因爲它們受到假設、風險和不確定性的影響,可能導致當前預期的結果和結果與實際結果不符,包括關於使用各種研究領域的大量整個人類基因組的技術的挑戰,以及在各種研究項目中涉及的難以發現的問題;成本或費用的意外增加;爲PacBio產品和正在開發中的產品供應元件或材料的中斷或延遲;潛在的產品性能和質量問題;第三方聲稱侵犯專利和專有權或試圖使PacBio的專利或專有權無效的權利和其他與國際業務有關的風險。這些前瞻性聲明基於當前預期,僅截至此日期;除法律要求外,PacBio不承擔修訂或更新這些前瞻性聲明以反映未來事件或情況的任何義務,即使有新信息可用也是如此。

Contacts
Investors:
Todd Friedman
ir@pacificbiosciences.com

聯繫方式
投資者:
Todd Friedman
ir@pacificbiosciences.com

SOURCE Pacific Biosciences of California, Inc.

資訊來源:pacific biosciences of california

譯文內容由第三人軟體翻譯。


以上內容僅用作資訊或教育之目的,不構成與富途相關的任何投資建議。富途竭力但無法保證上述全部內容的真實性、準確性和原創性。
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