Ianthe van Belzen Profile
Ianthe van Belzen

@IanthevanBelzen

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PhD student ~ Bioinformatics ~ Structural variant detection in pediatric cancer

Joined June 2009
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@IanthevanBelzen
Ianthe van Belzen
28 days
RT @emblebi: Osteosarcoma, an aggressive bone cancer, most commonly affects children and young adults. New research solves the mystery of…
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@IanthevanBelzen
Ianthe van Belzen
4 months
Our latest work on complex genomic rearrangements in pediatric cancer is available online! Many thanks @JayneHehirKwa @PatrickKemmeren @prinsesmaximac @KiKa8118
@CellGenomics
Cell Genomics
4 months
Complex structural variation is prevalent and highly pathogenic in pediatric solid tumors
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@IanthevanBelzen
Ianthe van Belzen
1 year
Happy to report our latest work on complex SVs in pediatric cancer is available as preprint! @JayneHehirKwa @PatrickKemmeren @prinsesmaximac
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@IanthevanBelzen
Ianthe van Belzen
2 years
@NS_online @ProRail @NS_online Reisplanner geeft aan dat sommige treinen rond 05:00 nog wel rijden en andere geannuleerd zijn. Als ik het bericht lees staat er "geen verkeer mogelijk" dus wordt de rest ook geannuleerd en raden jullie aan ander vervoer te nemen naar Schiphol?
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@IanthevanBelzen
Ianthe van Belzen
2 years
RT @svpino: 11 ways ChatGPT saves me hours of work every day, and why you'll never outcompete those who use AI effectively. A list for tho…
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@IanthevanBelzen
Ianthe van Belzen
2 years
In summary, we identified subgroups of 1q gain tumors with typical activated biological processes, indicating that integration of expression data is likely needed for further risk stratification of 1q gain Wilms tumors. (3/3)
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@IanthevanBelzen
Ianthe van Belzen
2 years
In summary, we identified subgroups of 1q gain tumors with typical activated biological processes, indicating that integration of expression data is likely needed for further risk stratification of 1q gain Wilms tumors. (3/3) @JayneHehirKwa @PatrickKemmeren @prinsesmaximac
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@IanthevanBelzen
Ianthe van Belzen
3 years
Interesting work! Imho understanding genetic variation is key to interpret the variants we find in disease e.g. cancer genomics
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@IanthevanBelzen
Ianthe van Belzen
3 years
RT @sedlazeck: Out today @GenomeBiology, we #Review the state of SV and summarized the efforts for #SEQC2. Also great catalog of resources…
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@IanthevanBelzen
Ianthe van Belzen
3 years
RT @camerongenomics: This is your regular reminder that the Hartwig cohort is an absolutely amazing resource and if you're doing any SV wor…
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@IanthevanBelzen
Ianthe van Belzen
3 years
RT @camerongenomics: StructuralVariantAnnotation finally has a publication associated with it. Ever wanted to compare SV call sets across m…
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@IanthevanBelzen
Ianthe van Belzen
3 years
@JayneHehirKwa Congratulations to @JayneHehirKwa @PatrickKemmeren and others involved. Great work! "Improved Gene Fusion Detection in Childhood Cancer Diagnostics Using RNA Sequencing"
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@IanthevanBelzen
Ianthe van Belzen
3 years
@HelloPhD Nice podcast and resource! I usually rely on my google scholar alerts, but going to try this 'academic twitter' thing - sounds promising for connecting to other scientists :)
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@IanthevanBelzen
Ianthe van Belzen
3 years
Our preprint is out! Fusion-sq is a method to detect and interpret gene fusions in pediatric cancer by resolving underlying structural variants and gene expression changes #genefusions #structuralvariants
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@IanthevanBelzen
Ianthe van Belzen
4 years
RT @BioSB_nl: Save the date! The #BioSB2021 conference is planned on 15-16 June 2021. Key dates, topics and call for abstracts will follow…
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