Bionano Announces Robust Presence at Upcoming Cytogenetics Conferences ESHG and ACC With 39 Scientific Presentations and Posters Highlighting the Utility of the Optical Genome Mapping Workflow
Bionano Announces Robust Presence at Upcoming Cytogenetics Conferences ESHG and ACC With 39 Scientific Presentations and Posters Highlighting the Utility of the Optical Genome Mapping Workflow
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A record 31 scientific presentations and posters at the 2024 European Society for Human Genetics (ESHG) Annual Conference and 8 scientific presentations and posters at the 2024 American Cytogenomics Conference (ACC) will highlight the application of optical genome mapping (OGM) in genetic disorder, rare disease, and cancer research applications
- Bionano will host a sponsored session at ESHG featuring an overview of the Company's OGM workflow delivered by Bionano's chief medical officer, Dr. Alka Chaubey, a presentation from Dr. Laura Batlle Masó at Vall d'Hebron Institute of Research (Spain) on OGM's potential utility in resolving hereditary angioedema (HAE) cases, a presentation from Dr. Bart van der Sanden at Radboud UMC (Netherlands) on how OGM may be useful for the detection of structural variants (SVs) relevant to rare disease, and a presentation from Marlene Ek at Karolinska Institute (Sweden) highlighting OGM's ability to unveil more cytogenomic insights into multiple myeloma samples than traditional cytogenetic methods
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At ACC, a sponsored session will feature Dr. Mike Gallagher, market development manager at Bionano, highlighting OGM's ability to enhance detection of pathogenic variants and to advance genetic disease research. Dr. Gallagher will also introduce the latest innovations in the OGM workflow, including the Stratys system and VIA software
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2024 年創紀錄的 31 場科學演講和海報 歐洲人類遺傳學會(ESHG)年會 以及8場科學演講和海報 2024 美國細胞基因組學會議 (ACC) 將重點介紹光學基因組映射(OGM)在遺傳疾病、罕見疾病和癌症研究應用中的應用
- Bionano將在ESHG主持一次贊助會議,由Bionano的首席醫學官Alka Chaubey博士概述公司的OGM工作流程,博士在演講中將概述公司的OGM工作流程 勞拉·巴特爾·馬索在 瓦爾·希伯倫研究所(西班牙)關於OGM在解決遺傳性血管性水腫(HAE)病例方面的潛在效用,博士的演講 巴特·範德桑登在 Radboud UMC(荷蘭)介紹了 OGM 如何可用於檢測與罕見疾病相關的結構變異(SV),以及來自 瑪琳·埃克在 卡羅林斯卡研究所(瑞典)強調了與傳統的細胞遺傳學方法相比,OGM有能力對多個骨髓瘤樣本提供更多的細胞基因組見解
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在ACC上,Bionano的市場開發經理邁克·加拉格爾博士將主持一場贊助會議,重點介紹 OGM 增強病原變異檢測和推進遺傳病研究的能力。加拉格爾博士還將介紹OGM工作流程的最新創新,包括Stratys系統和VIA軟件
SAN DIEGO, May 30, 2024 (GLOBE NEWSWIRE) -- Bionano Genomics, Inc. (Nasdaq: BNGO) today announced the Company's robust participation at two upcoming cytogenetics conferences, the 2024 European Society for Human Genetics (ESHG) Annual Conference and the 2024 American Cytogenomics Conference (ACC), with a record 39 scientific presentations and posters across the two conferences that highlight the utility of the Company's OGM workflow for applications in genetic disease, cancer, and rare disease research and discussing the latest advances to the Company's suite of products, including the high throughput Stratys system and VIA software.
聖地亞哥,2024年5月30日(GLOBE NEWSWIRE)——Bionano Genomics, Inc.(納斯達克股票代碼:BNGO)今天宣佈,該公司將積極參與即將舉行的兩次細胞遺傳學會議,即2024年歐洲人類遺傳學學會(ESHG)年會和2024年美國細胞基因組學會議(ACC),在這兩個會議上發表了創紀錄的39場科學演講和海報,重點介紹了公司OGM工作流程的效用用於遺傳病、癌症和罕見病研究的應用,並討論公司套件的最新進展產品,包括高吞吐量 Stratys 系統和 VIA 軟件。
ESHG brings together industry and academic professionals annually to discuss new technologies and advances in the field of human genetics. ESHG sessions will take place June 1-4, 2024 virtually and in Berlin, Germany.
ESHG 每年彙集行業和學術界專業人士,討論人類遺傳學領域的新技術和進步。ESHG 會議將於 2024 年 6 月 1 日至 4 日在德國柏林虛擬舉行。
ACC is a biennial conference focused on new technologies and advances in the field of cytogenetics. ACC will be held June 2-5, 2024 in Norfolk, Virginia.
ACC是兩年一次的會議,重點關注細胞遺傳學領域的新技術和進展。ACC 將於 2024 年 6 月 2-5 日在弗吉尼亞州的諾福克舉行。
Bionano will host a sponsored session at ESHG featuring an overview of the Company's OGM workflow delivered by Bionano's chief medical officer, Dr. Alka Chaubey, a presentation from Dr. Laura Batlle Masó at Vall d'Hebron Institute of Research (Spain) on OGM's potential utility in resolving hereditary angioedema (HAE) cases, a presentation from Dr. Bart van der Sanden at Radboud UMC (Netherlands) covering how OGM may be useful for the detection of SVs relevant to rare disease, and a presentation from Marlene Ek at Karolinska Institute (Sweden) highlighting OGM's ability to unveil more cytogenomic insights into multiple myeloma samples than traditional cytogenetic methods.
Bionano將在ESHG舉辦贊助會議,由Bionano的首席醫學官Alka Chaubey博士概述公司的OGM工作流程,西班牙瓦爾·希伯倫研究所的勞拉·巴特爾·馬索博士關於OGM在解決遺傳性血管性水腫(HAE)病例方面的潛在效用的演講,由UMBoud的巴特·範德桑登博士發表的演講 C(荷蘭)介紹了OGM如何可用於檢測與罕見疾病相關的SV,以及卡羅林斯卡研究所(瑞典)Marlene Ek的演講,重點介紹了OGM的演講與傳統的細胞遺傳學方法相比,能夠對多個骨髓瘤樣本提供更多的細胞基因組學見解。
At ACC, a sponsored session will feature Dr. Mike Gallagher, market development manager at Bionano, highlighting OGM's ability to enhance detection of pathogenic variants and to advance genetic disease research. Dr. Gallagher will also introduce the latest innovations in the OGM workflow, including the Stratys system and VIA software.
在ACC上,Bionano的市場開發經理邁克·加拉格爾博士將主講一場贊助的會議,重點介紹OGM增強致病變異檢測和推進遺傳病研究的能力。加拉格爾博士還將介紹OGM工作流程的最新創新,包括Stratys系統和VIA軟件。
Erik Holmlin, PhD, president and chief executive officer of Bionano, stated, "We are excited to see the progress that the global OGM community is making, which is highlighted by the growth in the number of scientific posters and presentations on OGM from the last time the ESHG and ACC conferences were held. We believe this expansion demonstrates the increased customer adoption of OGM, with routine and repeated utilization for innovative research into genetic disorders, cancer and rare disease."
Bionano總裁兼首席執行官埃裏克·霍爾姆林博士表示:“我們很高興看到全球OGM社區正在取得的進展,自上次舉行ESHG和ACC會議以來,有關OGM的科學海報和演講數量的增加突顯了這一點。我們認爲,此次擴張表明客戶越來越多地採用OGM,OGM可以常規和重複地用於遺傳疾病、癌症和罕見疾病的創新研究。”
ESHG scientific presentations and poster sessions:
ESHG 科學演講和海報發佈會:
Scientific presentations and poster sessions on OGM at ESHG take place in the exhibition halls unless otherwise noted.
除非另有說明,否則ESHG關於OGM的科學演講和海報發佈會在展廳舉行。
Abstract/ Poster Number | Title | Authors | Presented |
P14.015.A | Deciphering a complex short size RERE rearrangement: importance of combined approaches for duplication interpretation | Fauqueux J. | June 2, 2024 10:15-11:15 AM CEST |
P01.065.A | A Canadian lab's experience using optical genome mapping to clinically genotype hematological neoplasms | Hamadeh Z. | June 2, 2024 10:15-11:15 AM CEST |
P03.025.A | Characterization of a complex rearrangement between three chromosomes in a fetus with skeletal anomalies by optical genome mapping | Heinrich U. | June 2, 2024 10:15-11:15 AM CEST |
P16.077.A | Accurate identification of pathogenic structural variants guided by multi-platform comparison | Moeinzadeh M. | June 2, 2024 10:15-11:15 CEST |
P01.163.B | Deciphering the molecular complexity of the IKZF1 plus profile using optical genome mapping | Lühmann J. | June 2, 2024 16:45-17:45 PM CEST |
P12.023.B | SORD and SORD2P inversion: long read sequencing identifies a novel genetic mechanism underlying inherited neuropathy | Manini A. | June 2, 2024 16:45-17:45 PM CEST |
P04.029.B | Optical genome mapping facilitates rapid characterization of structural variants in families with developmental eye anomalies | Merepa S. | June 2, 2024 16:45-17:45 PM CEST |
P01.007.C | Large genomic rearrangement: tandem duplication and triplication in BRCA1 gene causative for hereditary breast and ovarian cancer | Aldrige Allister B. | June 3, 2024 10:15-11:15 AM CEST |
P15.102.C | Establishing ultra-rapid genome sequencing in neonatal and pediatric intensive care units in Germany – project Baby Lion | Auber B. | June 3, 2024 10:15-11:15 AM CEST |
P14.029.C | Optical genome mapping of a patient with ring chromosome 3 shows the importance of choosing the proper reference genome for the analysis | Burssed B. | June 3, 2024 10:15-11:15 AM CEST |
P14.025.C | Positive predictive value of balanced structural variants reported through short-read genome sequencing: do we need orthogonal confirmation? | Chatron N. | June 3, 2024 10:15-11:15 AM CEST |
P14.013.C | Optical genome mapping identifies hidden structural variants in 58 undiagnosed rare disease patient-parent trios | Hoischen A. | June 3, 2024 10:15-11:15 AM CEST |
P01.160.C | Deciphering copy number variations within the complex genomic region of the PMS2 gene using optical genome mapping | Maier J. | June 3, 2024 10:15-11:15 AM CEST |
P12.032.C | The WWOX gene variants detection in patient with cerebellar ataxia using optical genome mapping | Rutkowska K. | June 3, 2024 10:15-11:15 AM CEST |
P01.051.C | Enhanced cytogenomic analysis of complex karyotype in myelodysplastic syndrome using optical genome mapping | Valkama A. | June 3, 2024 10:15-11:15 AM CEST |
P21.065.D | Advancing genetic diagnostics: optical genome mapping's efficacy in identifying structural variants for autosomal recessive diseases | Beyza Ogutlu O. | June 3, 2024 16:45-17:45 PM CEST |
P15.079.D | Benefits of the analysis of a complex chromosomal rearrangement in the implementation of long read approaches | Chambon P. | June 3, 2024 16:45-17:45 PM CEST |
P04.011.D | A combined approach of innovative DNA- and RNA-technologies reveals hidden LINE-1/ERV insertion in IQCB1 as causative variant for Senior Løken syndrome | de Bruijn S. | June 3, 2024 16:45-17:45 PM CEST |
P01.056.D | Exome sequencing identified rare recurrent copy number variants and hereditary breast cancer susceptibility | Mantere T. | June 3, 2024 16:45-17:45 PM CEST |
P15.091.D | A multimodal approach to molecular diagnosis in NF1 highlights the need for bespoke analysis in undiagnosed patients | McAleese-Park E. | June 3, 2024 16:45-17:45 PM CEST |
P10.021.D | Optical genome mapping finally unveils the genetic cause of aniridia and intellectual disability in a 17-year-old after seven years of diagnostic odyssey | Telman W. | June 3, 2024 16:45-17:45 PM CEST |
E-poster | Optical genome mapping for comprehensive genomic rearrangement analysis | Flunkert J. | Online |
E-poster | Optical genome mapping: lighting the way in complex clinical cases | Monge Lobo I. | Online |
E-poster | Refining genotype-phenotype correlation in complex chromosomal rearrangements using optical genome mapping – case report | Vallova V. | Online |
E-poster | Unraveling the mysteries of balanced rearrangements: optical genome mapping spotlights BCL11B misregulation in a familial translocation | Alcalá San Martín A. | Online |
E-poster | Optical genome mapping (OGM) allows the characterization of a complex chromosome rearrangement associated with recurrent pregnancy loss | Trost D. | Online |
E-poster | Focus on deletions and duplications identified by optical genome mapping technique in a cohort of 100 patients: comparison with MCA | Doco-Fenzy M. | Online |
Room | Title | Presenter | Presented |
Poster presentation | Optical genome mapping identifies hidden structural variants in previously undiagnosed rare disease cases in Solve-RD | van der Sanden B. | June 1, 2024 19:00-19:15 PM CEST, Room A8 |
Poster presentation | Multiomics and deep phenotyping in MECP2 Duplication syndrome: insight into disease severity, expression variability, and nucleic acid therapeutics | Pehlivan D. | June 1, 2024 19:45-20:00 PM CEST, Room A8 |
Poster presentation | Next generation cytogenetics by optical genome mapping | Kanagal-Shamanna R. | June 3, 2024 08:30-10:00 AM CEST, Room A2 |
Sponsored session | Insights into constitutional disorders and beyond: scaling to new heights with optical genome mapping | Chaubey A., Batlle Masó L., van der Sanden B., Ek M. | June 3, 2024 14:00-15:30 PM CEST Room New York 3 (Level 1) |
摘要/ 海報 數字 | 標題 | 作者 | 已提交 |
P14.015.A | 破譯複雜的短尺寸 RERE 重排:採用組合方法進行重複解釋的重要性 | Fauqueux J. | 2024 年 6 月 2 日 美國中部標準時間上午 10:15-11:15 |
P01.065.A | 加拿大實驗室使用光學基因組映射對血液腫瘤進行臨床基因分型的經驗 | 哈馬德 Z. | 2024 年 6 月 2 日 美國中部標準時間上午 10:15-11:15 |
P03.025.A | 通過光學基因組映射表徵骨骼異常胎兒中三條染色體之間的複雜重排 | 海因裏希·U. | 2024 年 6 月 2 日 美國中部標準時間上午 10:15-11:15 |
P16.077.A | 通過多平台比較精確識別致病結構變異 | Moeinzadeh M. | 2024 年 6 月 2 日 歐洲中部標準時間 10:15-11:15 |
P01.163.B | 使用光學基因組映射解密 IKZF1 plus 配置文件的分子複雜性 | 盧曼 J. | 2024 年 6 月 2 日 歐洲中部標準時間下午 16:45-17:45 |
P12.023.B | SORD 和 SORD2P 反轉:長讀測序確定了遺傳性神經病背後的新遺傳機制 | 馬尼尼 A. | 2024 年 6 月 2 日 歐洲中部標準時間下午 16:45-17:45 |
P04.029.B | 光學基因組圖譜有助於快速表徵眼發育異常家族的結構變異 | 梅雷帕 S. | 2024 年 6 月 2 日 歐洲中部標準時間下午 16:45-17:45 |
P01.007.C | 大型基因組重排:導致遺傳性乳腺癌和卵巢癌的 BRCA1 基因的串聯複製和三重複制 | Aldrige Allister B. | 2024年6月3日 美國中部標準時間上午 10:15-11:15 |
P15.102.C | 在德國的新生兒和兒科重症監護室建立超快速基因組測序——項目 Baby Lion | 奧伯 B. | 2024年6月3日 美國中部標準時間上午 10:15-11:15 |
P14.029.C | 對3號環狀染色體患者的光學基因組圖譜顯示了選擇合適的參考基因組進行分析的重要性 | 已發放助金 B. | 2024年6月3日 美國中部標準時間上午 10:15-11:15 |
P14.025.C | 通過短讀基因組測序報告的平衡結構變異的積極預測價值:我們需要正交確認嗎? | 查特龍 N. | 2024年6月3日 美國中部標準時間上午 10:15-11:15 |
P14.013.C | 光學基因組映射可識別58例未確診的罕見病患者家長三人組中隱藏的結構變異 | Hoischen A. | 2024年6月3日 美國中部標準時間上午 10:15-11:15 |
P01.160.C | 使用光學基因組映射解密 PMS2 基因複雜基因組區域內的拷貝數變化 | 邁爾 J. | 2024年6月3日 美國中部標準時間上午 10:15-11:15 |
P12.032.C | 使用光學基因組映射檢測小腦共濟失調患者的WWOX基因變異 | 魯特科夫斯卡 K. | 2024年6月3日 美國中部標準時間上午 10:15-11:15 |
P01.051.C | 使用光學基因組映射增強骨髓增生異常綜合徵複雜核型的細胞基因組分析 | 瓦爾卡瑪 A. | 2024年6月3日 美國中部標準時間上午 10:15-11:15 |
P21.065.D | 推進遺傳診斷:光學基因組映射在識別常染色體隱性遺傳疾病結構變異方面的功效 | Beyza Ogutlu O. | 2024年6月3日 歐洲中部標準時間下午 16:45-17:45 |
P15.079.D | 分析複雜染色體重排對實施長讀方法的好處 | Chambon P. | 2024年6月3日 歐洲中部標準時間下午 16:45-17:45 |
P04.011.D | 創新 DNA 和 RNA 技術的組合方法顯示,IQCB1 中隱藏的 LINE-1/ERV 插入是 Senior Löken 綜合徵的病原變體 | de Brujn S. | 2024年6月3日 歐洲中部標準時間下午 16:45-17:45 |
P01.056.D | 外顯子組測序發現了罕見的復發拷貝數變異和遺傳性乳腺癌易感性 | 曼特雷 T. | 2024年6月3日 歐洲中部標準時間下午 16:45-17:45 |
P15.091.D | 1型神經纖維瘤病分子診斷的多模態方法凸顯了對未確診患者進行定製分析的需求 | 麥卡利斯公園 E. | 2024年6月3日 歐洲中部標準時間下午 16:45-17:45 |
P10.021.D | 經過七年的診斷之旅,光學基因組測繪終於揭示了一名17歲孩子的Aniridia和智力障礙的遺傳原因 | 特爾曼 W. | 2024年6月3日 歐洲中部標準時間下午 16:45-17:45 |
電子海報 | 用於全面基因組重排分析的光學基因組映射 | Flunkert J. | 在線 |
電子海報 | 光學基因組映射:爲複雜的臨床病例點亮道路 | Monge Lobo I. | 在線 |
電子海報 | 使用光學基因組映射改善複雜染色體重排中的基因型表型相關性——病例報告 | Vallova V. | 在線 |
電子海報 | 揭開平衡重排的奧秘:光學基因組映射聚焦家族異位中的 BCL11B 失調 | 阿爾卡拉聖馬丁 A. | 在線 |
電子海報 | 光學基因組映射(OGM)允許表徵與複發性流產相關的複雜染色體重排 | 特羅斯特 D. | 在線 |
電子海報 | 重點研究通過光學基因組映射技術在100名患者隊列中識別的缺失和重複:與MCA的比較 | Doco-Fenzy M. | 在線 |
房間 | 標題 | 演示者 | 已提交 |
海報演示 | 光學基因組映射可識別Solve-RD中先前未診斷的罕見疾病病例中隱藏的結構變異 | 範德桑登 B. | 2024年6月1日 美國中部標準時間下午 19:00-19:15, A8 房間 |
海報演示 | MECP2 重複綜合徵的多組學和深度表型分析:深入了解疾病嚴重程度、表達變異性和核酸療法 | Pehlivan D. | 2024年6月1日 美國中部標準時間下午 19:45-20:00, A8 房間 |
海報演示 | 通過光學基因組映射實現下一代細胞遺傳學 | Kanagal-Shamanna R. | 2024年6月3日 美國中部標準時間上午 08:30-10:00, A2 房間 |
贊助會議 | 對體質障礙及其他問題的見解:通過光學基因組映射擴展到新的高度 | Chaubey A.、Batlle Masoé L.、van der Sanden B.、Ek M. | 2024年6月3日 美國中部標準時間下午 14:00-15:30 紐約 3 號房(第 1 層) |
ACC scientific presentations and poster sessions:
ACC 科學演講和海報發佈會:
Scientific presentations and poster sessions on OGM at ACC take place in the exhibition hall.
ACC關於OGM的科學演講和海報發佈會在展廳舉行。
Poster/Presentation | Title | Presenter | Presented |
Exhibitor theater session | Revolutionizing cytogenomics with optical genome mapping: high-resolution structural variant detection with an elevated sample-to-answer workflow | Gallagher M. | June 3, 2024 12:15-12:35 PM EST |
Poster presentation | Enhanced detection of primary oncogenic drivers in pediatric T-lymphoblastic leukemia (T-ALL) by optical genome mapping (OGM) | Raca G. | June 3, 2024 2:00-2:15 PM EST |
Poster presentation | Utility of optical genome mapping as an additional tool to standard cytogenetic workup in hematological malignancies | Toruner G. | June 3, 2024 2:15-2:30 PM EST |
Poster presentation | A curated research catalogue of structural variation from 809 postnatal cases detected by optical genome mapping | Pang A. | June 3, 2024 4:00-4:15 PM EST |
Poster presentation | A search for genetic determinants in neural tube defects using optical genome mapping | Sahajpal N. | June 3, 2024 4:15-4:30 PM EST |
Poster presentation | Cross-comparison of optical genome mapping and chromosomal microarray data using VIA software | Yu J. | June 3, 2024 4:30-4:45 PM EST |
Poster hall | Efficient hematological malignancy analysis and reporting workflow using optical genome mapping | Clifford B. | |
Poster hall | Isotachophoresis (ITP) for high-throughput isolation of UHMW gDNA suitable for optical genome mapping (OGM) | Yadav M. |
海報/演示文稿 | 標題 | 演示者 | 已提交 |
參展商劇院會議 | 通過光學基因組映射徹底改變細胞基因組學:通過更高的樣本到答案的工作流程進行高分辨率結構變異檢測 | 加拉格爾 M. | 2024年6月3日 美國東部時間下午 12:15-12:35 |
海報演示 | 通過光學基因組映射 (OGM) 增強對兒科 T 淋巴細胞白血病 (T-ALL) 主要致癌驅動因素的檢測 | 拉卡 G. | 2024年6月3日 美國東部標準時間下午 2:00-2:15 |
海報演示 | 光學基因組映射作爲血液系統惡性腫瘤標準細胞遺傳學檢查的附加工具的實用性 | Toruner G. | 2024年6月3日 美國東部時間下午 2:15-2:30 |
海報演示 | 通過光學基因組映射檢測到的809例產後病例的結構變異精選研究目錄 | Pang A. | 2024年6月3日 美國東部標準時間下午 4:00-4:15 |
海報演示 | 使用光學基因組映射搜索神經管缺陷中的遺傳決定因素 | Sahajpal N. | 2024年6月3日 美國東部時間下午 4:15-4:30 |
海報演示 | 使用 VIA 軟件交叉比較光學基因組映射和染色體微陣列數據 | Yu J. | 2024年6月3日 美國東部時間下午 4:30-4:45 |
海報大廳 | 使用光學基因組映射進行高效的血液學惡性腫瘤分析和報告工作流程 | 克利福德 B. | |
海報大廳 | 等位電泳 (ITP) 用於高通量分離適用於光學基因組映射 (OGM) 的 UHMW gDNA | 亞達夫 M. |
More details on Bionano's presence at the ESHG conference can be found here, and virtual posters will be shown here; more details on Bionano's presence at the ACC conference can be found here.
About Bionano
關於 Bionano
Bionano is a provider of genome analysis solutions that can enable researchers and clinicians to reveal answers to challenging questions in biology and medicine. The Company's mission is to transform the way the world sees the genome through OGM solutions, diagnostic services and software. The Company offers OGM solutions for applications across basic, translational and clinical research. The Company also offers an industry-leading, platform-agnostic genome analysis software solution and nucleic acid extraction and purification solutions using proprietary isotachophoresis (ITP) technology. Through its Lineagen, Inc. d/b/a Bionano Laboratories business, the Company also offers OGM-based diagnostic testing services. For more information, visit www.bionano.com, www.bionanolaboratories.com or www.purigenbio.com.
Bionano是基因組分析解決方案的提供商,該解決方案可以使研究人員和臨床醫生揭示生物學和醫學中具有挑戰性的問題的答案。該公司的使命是通過OGM解決方案、診斷服務和軟件改變世界看待基因組的方式。該公司爲基礎研究、轉化研究和臨床研究的應用提供OGM解決方案。該公司還提供行業領先的、與平台無關的基因組分析軟件解決方案以及使用專有的等位電泳(ITP)技術的核酸提取和純化解決方案。通過其Lineagen, Inc. d/b/a Bionano Laboratories業務,該公司還提供基於OGM的診斷測試服務。欲了解更多信息,請訪問 www.bionano.com, www.bionanolaboratories.com 要麼 www.purigenbio.com。
Unless specifically noted otherwise, Bionano's OGM products are for research use only and not for use in diagnostic procedures.
除非另有特別說明,否則Bionano的OGM產品僅用於研究用途,不用於診斷程序。
Forward-Looking Statements of Bionano
Bionano 的前瞻性陳述
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Words such as "ability," "believe," "may," "potential," "will," and similar expressions (as well as other words or expressions referencing future events, conditions or circumstances) convey uncertainty of future events or outcomes and are intended to identify these forward-looking statements. Forward-looking statements include statements regarding our intentions, beliefs, projections, outlook, analyses or current expectations concerning, among other things, OGM's utility for genetic disorder, rare disease, and cancer research applications; OGM's ability and utility for resolving HAE cases; the ability and utility of OGM to detect SVs relevant to rare disease; the ability of OGM to unveil more cytogenomic insights into multiple myeloma samples than traditional cytogenetic methods; OGM's ability to enhance detection of pathogenic variants and to advance genetic disease research; the utility of the latest innovations in OGM workflows, including the Stratys system and VIA software; the utility of OGM for research in the areas reported in the presentations given and the posters made available at the ESHG Annual Conference 2024 and AAC 2024; the growth and adoption of OGM for use in genetic disorder, rare disease, and cancer research applications; the ability and utility of our OGM solutions to drive market adoption of OGM; and any other statements not of historical fact. Each of these forward-looking statements involves risks and uncertainties. Actual results or developments may differ materially from those projected or implied in these forward-looking statements. Factors that may cause such a difference include the risks and uncertainties associated with: global and macroeconomic events, such as the impact of the global pandemics, bank failures, interest rate changes, supply disruptions, and the ongoing conflicts in the Ukraine and Russia and between Israel and Hamas, and related sanctions, on our business and the global economy; general market conditions; changes in the competitive landscape and the introduction of competitive technologies or improvements to existing technologies; the failure of OGM's utility for genetic disorder, rare disease, and cancer research applications; the failure of OGM to resolve HAE cases; the failure of OGM to detect SVs relevant to rare disease; the failure of OGM to unveil more cytogenomic insights into multiple myeloma samples than traditional cytogenetic methods; the failure of OGM to enhance detection of pathogenic variants and to advance genetic disease research; the failure of our latest innovations in OGM workflows, including the Stratys system and VIA software; the failure of OGM for research in the areas reported in the presentations given and the posters made available at the ESHG Annual Conference 2024 and AAC 2024; the growth and adoption of OGM for use in genetic disorder, rare disease, and cancer research applications; the ability and utility of our OGM solutions to drive market adoption of OGM; the ability of our OGM solutions to offer the anticipated benefits for and contributions to the areas reported in the presentations given and posters made available at the ESHG Annual Conference 2024 and AAC 2024; future study results contradicting the results reported in the presentations given and posters made available at the ESHG Annual Conference 2024 and AAC 2024; changes in our strategic and commercial plans; our ability to obtain sufficient financing to fund our strategic plans and commercialization efforts; the ability of medical and research institutions to obtain funding to support adoption or continued use of our technologies; our ability to obtain sufficient financing to fund our strategic plans and commercialization efforts and to continue as a "going concern"; and the risks and uncertainties associated with our business and financial condition in general, including the risks and uncertainties described in our filings with the Securities and Exchange Commission, including, without limitation, our Annual Report on Form 10-K for the year ended December 31, 2023 and in other filings subsequently made by us with the Securities and Exchange Commission. All forward-looking statements contained in this press release speak only as of the date on which they were made and are based on management's assumptions and estimates as of such date. We do not undertake any obligation to publicly update any forward-looking statements, whether as a result of the receipt of new information, the occurrence of future events or otherwise.
本新聞稿包含1995年《私人證券訴訟改革法》所指的前瞻性陳述。諸如 “能力”、“相信”、“可能”、“潛力”、“意願” 之類的詞語和類似表達(以及其他提及未來事件、條件或情況的詞語或表達)傳達了未來事件或結果的不確定性,旨在識別這些前瞻性陳述。前瞻性陳述包括有關我們的意圖、信念、預測、展望、分析或當前預期的陳述,除其他外,OGM在遺傳疾病、罕見病和癌症研究應用方面的效用;OGM在解決HAE病例方面的能力和效用;OGM檢測與罕見病相關的SV的能力和效用;OGM能夠比傳統的細胞遺傳學方法對多個骨髓瘤樣本提供更多細胞基因組見解;M 增強對致病變異的檢測和進步的能力遺傳病研究;OGM工作流程最新創新的實用性,包括Stratys系統和VIA軟件;OGM在2024年ESHG年會和AAC 2024年年會上發表的演講和海報中報告的領域中的研究效用;OGM在遺傳疾病、罕見疾病和癌症研究應用中的發展和採用;我們的OGM解決方案推動OGM市場採用的能力和效用;以及任何其他與歷史事實無關的陳述。這些前瞻性陳述都涉及風險和不確定性。實際業績或發展可能與這些前瞻性陳述中的預測或暗示存在重大差異。可能導致這種差異的因素包括與以下相關的風險和不確定性:全球和宏觀經濟事件,例如全球疫情、銀行倒閉、利率變化、供應中斷、烏克蘭和俄羅斯以及以色列和哈馬斯之間的持續衝突以及相關制裁對我們的業務和全球經濟的影響;總體市場狀況;競爭格局的變化以及競爭技術的引入或現有技術的改進;OGM的失敗對遺傳學的效用疾病、罕見病和癌症研究應用;OGM 未能解決 HAE 病例;OGM 未能檢測出與罕見疾病相關的簡易病毒;OGM 未能比傳統的細胞遺傳學方法對多個骨髓瘤樣本提供更多的細胞基因組見解;OGM 未能加強對致病變異的檢測和推進遺傳病研究;我們在OGM工作流程方面的最新創新失敗,包括Stratys 系統和VIA軟件;OGM未能在演示文稿中報告的領域進行研究以及在2024年ESHG年會和AAC 2024年年會上發佈的海報;OGM在遺傳疾病、罕見疾病和癌症研究應用中的發展和採用;我們的OGM解決方案推動OGM市場採用的能力和效用;我們的OGM解決方案爲2024年ESHG年會和AAC 2024年未來年會上的演講和海報中報告的領域提供預期收益和貢獻的能力;研究結果與所給演示文稿中報告的結果相矛盾在2024年ESHG年會和AAC 2024年會上發佈的海報;我們戰略和商業計劃的變化;我們獲得足夠資金以資助我們的戰略計劃和商業化工作的能力;醫療和研究機構獲得資金以支持採用或繼續使用我們的技術的能力;我們獲得足夠資金來資助我們的戰略計劃和商業化工作並繼續作爲 “持續企業” 的能力;以及與我們的業務和財務相關的風險和不確定性條件總體而言,包括我們在向美國證券交易委員會提交的文件中描述的風險和不確定性,包括但不限於我們截至2023年12月31日止年度的10-K表年度報告以及我們隨後向美國證券交易委員會提交的其他文件中描述的風險和不確定性。本新聞稿中包含的所有前瞻性陳述僅代表截至發表之日,並基於管理層截至該日的假設和估計。我們不承擔任何義務公開更新任何前瞻性陳述,無論是收到新信息、未來事件發生還是其他原因。
CONTACTS
聯繫人
Company Contact:
Erik Holmlin, CEO
Bionano Genomics, Inc.
+1 (858) 888-7610
eholmlin@bionano.com
公司聯繫人:
埃裏克·霍爾姆林,首席執行官
Bionano Genomics, Inc.
+1 (858) 888-7610
eholmlin@bionano.com
Investor Relations:
David Holmes
Gilmartin Group
+1 (858) 888-7625
IR@bionano.com
投資者關係:
大衛霍姆斯
吉爾馬丁集團
+1 (858) 888-7625
IR@bionano.com
Source: Bionano Genomics
來源:Bionano Genomics