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Gene fault linked to severe Covid risk in young people: Study

Gene fault linked to severe Covid risk in young people: Study
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Alexander hoischenRadboud university medical centre

Bionano Genomics Hosts Day 1 of 2022 Symposium with Six Presentations Highlighting the Superior Performance of OGM in Variant Detection for Constitutional Genetic Diseases

Bionano Genomics Hosts Day 1 of 2022 Symposium with Six Presentations Highlighting the Superior Performance of OGM in Variant Detection for Constitutional Genetic Diseases
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United statesJuniper pointMiriam bornhorstMichael sullivanChaim jalasAlexander hoischenLaila el khattabiShirley heggartyErik holmlinCatherinea brownsteinAmy conradNikhil sahajpalAlka chaubeyExchange commissionAugusta universityCompany contact

Bionano Genomics Hosts Day 1 of 2022 Symposium with Six Presentations Highlighting the Superior Performance of OGM in Variant Detection for Constitutional Genetic Diseases

11.01.2022 - SAN DIEGO, Jan. 10, 2022 (GLOBE NEWSWIRE) - Bionano Genomics, Inc. (BNGO), pioneer of optical genome mapping (OGM) solutions on the Saphyr system and provider of NxClinical, the leading software solutions for visualization, interpretation and . Seite 1

Shirley heggartyNikhil sahajpalAlexander hoischenAugusta university

Bionano Genomics Announces the Final Speaker Lineup for 2022 Symposium

Bionano Genomics Announces the Final Speaker Lineup for 2022 Symposium
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New yorkUnited statesFrance generalUnited kingdomRegion flamandeSan diegoSan antonioColumbia universityUniversity of rochester medical centerComunidad autonoma de catalunaNew jerseyBence dvorakChaim jalasAdrian dubucSelena garcShirley heggarty

Optical genome mapping could change the existing workflow within cytogenetic laboratories

Optical genome mapping could change the existing workflow within cytogenetic laboratories Dutch-French research shows that Optical Genome Mapping (OGM) detects abnormalities in chromosomes and DNA very quickly, effectively and accurately. Sometimes even better than all existing techniques together, as they describe in two proof-of-concept studies published in the American Journal of Human Genetics. This new technique could radically change the existing workflow within cytogenetic laboratories. Human hereditary material is stored in 46 chromosomes (23 pairs). Although those chromosomes are quite stable, changes in number or structure can still occur. A well-known example is Down syndrome, which is caused by an extra chromosome 21 (trisomy 21). An extra chromosome makes a big difference and is quite easy to visualize. But all kinds of other, smaller changes can occur as well in chromosomes.

United statesFrance generalMarian stevens kroefEl khattabiAlexander hoischenEmily hendersonRadboud university medical center radboudumcClinical laboratory geneticistOptical genome mappingAmerican journalCopy number variantGenome mappingRadboud university medical centerGenomics technologiesHuman geneticsNext generation cytogenetic