BIONANO GENOMICS DL-,0001 Forum: Community User: Shruikan

Hab nochmal 1500 Aktien geholt konnte nicht sitzenlassen das der mehr hat wie ich, sagt er einfach, „ Vorsicht, ich könnte auch noch mehr kaufen“ Würde ja jetzt gern das kaufrennen weiter machen, aber hab nicht des Geld rumfliegen was der Millionär hat 😞

Guten Abend Gang. Unser Mädel macht heute nur eine Verschnaufpause, oder Per?😁

these updates are significant improvements in variant detection, as well as workflow simplifications and other benefits designed to support clinical research in inherited genetic diseases and cancer. All new Saphyr system installations will include these versions. New OGM capabilities include the means to detect more clinically-relevant variants such as absence of heterozygosity (AOH) and allelic imbalance, the first two classes of variations that are typically considered as sequence rather than structural variants. The updates will also enable users to visualize chromosomal AOH across the genome similarly to single nucleotide polymorphism (SNP) microarrays. In addition, OGM users will have the ability to detect uniparental isodisomy UPD, regions identical by decent (IBD), triploidy and improved characterization of mosaic SVs through variant allele fraction (VAF) plots. Also as part of this release, the family of EnFocus™ targeted analysis panels now includes one for Fragile X, a repeast expansion disorder. EnFocus Fragile X is an analytical routine that automates the process of sizing the Fragile X repeat with high accuracy, precision and sensitivity, thereby reducing the time to results for researchers. Bionano has streamlined the analytical workflow tied to OGM through this software release. The new workflow enables all SVs detected by Solve and analyzed with Access to be named and classified using standard terminology according to the 2020 International System for Human Cytogenomic Nomenclature (ISCN). This new classification is expected to simplify the reporting and interpretation of research findings, making it easier to compare information across other databases. “These ongoing improvements in the performance of our software for detecting SVs, as well as the tools for interpreting and reporting calls, continue to impress me,” said Erik Holmlin, PhD, CEO of Bionano Genomics. “We believe this update is significant because of the AOH and allelic imbalance functionality we are introducing. With our acquisition of BioDiscovery now complete, we can begin work to integrate our variant detection technology with NxClinical’s visualization, interpretation and reporting capabilities to offer a potentially outstanding window through which researchers can obtain the data to drive their science.”

BIONANO GENOMICS ANNOUNCES MAJOR UPDATES TO ITS SOLVE™ AND ACCESS™ DATA SOLUTIONS ADDING SIGNIFICANT NEW VARIANT DETECTION, ANALYSIS AND REPORTING CAPABILITIES FOR OPTICAL GENOME MAPPING ON THE SAPHYR® SYSTEM

Gute Nachrichten 👍🏻

Normal müsste die H1 candle in rot heute mit einer grünen gegengesteuert werden sprich 6,20 $ also Ziel heute . Beobachten ;)

5,82 liegt ne line ;)

Widerstand aufgebaut hoch gehts ;)

Da hat wohl wieder wem die Trendumkehr nicht gepasst

Ja Per …. To the Moon

Bin heiß 😎

Habt ihr Bock ? :) Luft und Lust ist nach oben genug ;)

Moinsen ihr Raketenzwerge :)

Moin! Darf gerne nochmal sinken. 2022 wäre dann aber nachhaltiger Anstieg ziemlich nett 😃

Morgen Gang, Bis zu den Earnings könnte es noch steigen aber dann bin ich wieder vorsichtig 🙄🙄