#StructuralVariants
📄 Variant Calling in the Dark Genome: Benchmarking SNV Calls in the Flanks of Structural Variants

academic.oup.com/gpb/advance-...
#Genomics #VariantCalling #StructuralVariants #Bioinformatics #LongReadSequencing #HumanGenomics 6/6
Validate User
academic.oup.com
September 11, 2026 at 7:30 AM
To learn more about this useful tool, watch a live demo during the #ERGA #BioGenome Analysis & Applications Seminar last November:
▶️ youtube.com/live/Nve8LGJ...

#Biodiversity #genomics #structuralvariants #science #seminar
@irbio-ub.bsky.social @bsc-cns.bsky.social
PerSVade: personalized structural variant detection in any species of interest
YouTube video by ERGA - European Reference Genome Atlas
youtube.com
February 19, 2025 at 9:02 AM
New NIOO publication: Structural genomic variation and migratory behavior in a wild #songbird, by @HenkvanderJeugd and others.
#biodiversity #structuralvariants #birdmigration
https://doi.org/10.1093/evlett/qrad040
December 3, 2024 at 12:05 AM
Learn from experts in long-read sequencing with our on-demand webinar: "Maximizing Genomic Insights." Explore how advanced sequencing reveals complex genetic regions.

Watch now: https://bit.ly/41ABgF2

#LongReadSequencing #Genomics #StructuralVariants #ResearchInnovation #GenomicsInsights
December 17, 2025 at 8:05 AM
Learn from experts in long-read sequencing with our on-demand webinar: "Maximizing Genomic Insights." Explore how advanced sequencing reveals complex genetic regions.

Watch now: https://bit.ly/41ABgF2

#LongReadSequencing #Genomics #StructuralVariants #ResearchInnovation #GenomicsInsights
October 15, 2025 at 7:05 AM
Learn from our experts in long-read sequencing with our on-demand webinar: "Maximizing Genomic Insights." Explore how our advanced sequencing reveals complex genetic regions.

Watch now: bit.ly/41ABgF2

#LongReadSequencing #Genomics #StructuralVariants #ResearchInnovation #GenomicsInsights
January 6, 2025 at 8:33 AM
🚀 Thrilled to share our new review on how structural variants reshape 3D genome architecture and cause disease! 🧬🔀
Out now in Nature Reviews Genetics: www.nature.com/articles/s41...
#3D-Genome #StructuralVariants #uksh
Structural variants in the 3D genome as drivers of disease - Nature Reviews Genetics
Disruption of the 3D genome caused by structural variation contributes to developmental disorders and cancer. The authors review the causes and molecular and clinical consequences of position effects ...
www.nature.com
July 7, 2025 at 11:12 AM
Joining us at Maxwell in Focus is Bronwen Laugharne, from Oxford Nanopore Technologies - Population-scale structural variant analysis using ONT.

This is a free event, on 9 June 2026, in London

Register at: https://ow.ly/wRLe50YWL5u

#MaxwellInFocus #StructuralVariants
June 3, 2026 at 8:05 AM
🧬 New poster alert!
Discover how Dovetail® LinkPrep™ tech + Dovetail Precise enable 90% recall of somatic structural variants with base-pair precision — detecting deletions, duplications, inversions & translocations in a single assay.
📄 ow.ly/qaWf50XwvG7
#StructuralVariants #CancerGenomics
December 2, 2025 at 11:41 AM
🧬 Let’s talk structural variants!
🚨 TOMORROW, June 3rd — Webinar:
Uncover the Hidden Genome: SV Detection with Dovetail® LinkPrep!
🕙 10AM SGT | 12PM AEST
💡 One assay. Every variant—SVs, SNVs, InDels & CNVs
🔗 Register now: edenrocsciences.zoom...
#StructuralVariants #LinkPrep
June 2, 2025 at 2:00 AM
I'll be at #FoG2026 in London, for @dtgenomics.bsky.social . I look forward to seeing many familiar faces there and hope to meet some new ones. Let me know if you are attending and would like to catch up?
#3DGenomics #Epigenomics #StructuralVariants
January 20, 2026 at 2:30 PM
Join us in beautiful #Heidelberg to discover the most precise method for detecting all Structural Variants in a single reaction. We look forward to seeing you there!
#StructuralVariants #EnhancerHijacking #HiC #LinkPrep #SVs #EMBLCanGen
We’re excited to be part of the EMBL Conference: Cancer Genomics 2025!

💬 Learn how Dovetail® LinkPrep™ tech empowers cancer research through base pair–resolved variant detection, high-resolution 3D genome mapping, and comprehensive genomic profiling.

We look forward to connecting in Heidelberg!
November 11, 2025 at 12:42 PM
This week: representatives from Myriad Genetics & @pacbio.bsky.social demonstrate how their long-read sequencing approach successfully improves prenatal carrier screening: event.on24.com/wcc/r/525686...

#Diagnostics #Genetics #StructuralVariants #PacBio #MyriadGenetics #PrenatalScreening
March 24, 2026 at 5:46 PM
Learn how long-read sequencing assays are being deployed to improve prenatal carrier screening: event.on24.com/wcc/r/525686...

#Diagnostics #Genetics #StructuralVariants #PacBio #MyriadGenetics #PrenatalScreening
March 5, 2026 at 6:21 PM
Attendees will see how their computational workflow leverages PacBio PureTarget long-read sequencing assay to resolve difficult genetic structural variations and improve the accuracy of Myriad’s Foresight® Carrier Screen.

#StructuralVariants #PacBio #MyriadGenetics
January 6, 2026 at 8:24 PM
Pangenomic structural variant patterns reflect evolutionary diversification in Brassica napus. #StructuralVariants #Pangenomes #BrasicaNapusGenome #PlantGenomics #Bioinformatics #GenomeBiology 🧪🧬 🖥️
link.springer.com/article/10.1...
December 5, 2025 at 9:31 AM
The value of structural variants to conservation genomics in the pangenome era. #StructuralVariants #SVs #Bioinformatics #Genomics #ConservationGenomics #Pangenomes #JournalOfHeredity
academic.oup.com/jhered/advan...
December 2, 2025 at 6:05 PM
OctopuSV and TentacleSV: a one-stop toolkit for multi-sample, cross-platform structural variant comparison and analysis. #StructuralVariants #SVs #SVcomparison #SVidentification #Bioinformatics 🧪🧬 🖥️
academic.oup.com/bioinformati...
November 15, 2025 at 8:32 AM
insilicoSV: a flexible grammar-based framework for structural variant simulation and placement. #StructuralVariants #SVs #SVsimulation #SimulatedData #Genomics #Bioinformatics 🧪🧬 🖥️
academic.oup.com/bioinformati...
November 9, 2025 at 8:05 PM
Svirlpool: structural variant detection from long read sequencing by local assembly. #LongRead #Sequencing #LRS #StructuralVariants #SVs @biorxivpreprint.bsky.social
www.biorxiv.org/content/10.1...
November 8, 2025 at 9:31 AM
Complex de novo structural variants are an underestimated cause of rare disorders. #StructuralVariants #DeNovoSVs #RareDiseases #VariantsUnderstimation #Genomics #Bioinformatics @natcomms.nature.com 🧪🧬 🖥️
www.nature.com/articles/s41...
November 4, 2025 at 11:42 PM
Complete genome assemblies of two mouse subspecies reveal structural diversity of telomeres and centromeres. #MouseGenomes #StructuralVariants #TsT #Centromeres #Genomics @natgenet.nature.com
www.nature.com/articles/s41...
October 27, 2025 at 2:49 PM
October 25, 2025 at 7:32 AM
October 21, 2025 at 3:54 PM