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Paper Details

Omics-informed CNV calls reduce false-positive rates and improve power for CNV-trait associations.
HGG Adv
2
2022
CNV, CNVs, Copy-number variations, OQS, PennCNV, pCNV, pCNVs
Author NameAffiliation
Andrew P MorrisInstitute of Genomics, University of Tartu
Andrew P MorrisThe University of Manchester
Andrew P MorrisInstitute of Genomics, University of Tartu
Andrew P MorrisThe University of Manchester
Murielle BochudCenter for Primary Care and Public Health (Unisante), University of Lausanne
Murielle BochudCenter for Primary Care and Public Health (Unisante), University of Lausanne
Cisca WijmengaUniversity of Groningen, University Medical Center Groningen
Lude FrankeUniversity of Groningen, University Medical Center Groningen
Lude FrankeOncode Institute
Hedi PetersonInstitute of Computer Science, University of Tartu
Jaak ViloInstitute of Computer Science, University of Tartu
Reedik MägiInstitute of Genomics, University of Tartu
Zolt??n KutalikUniversity of Lausanne
Zolt??n Kutalik
Zolt??n KutalikCenter for Primary Care and Public Health (Unisante), University of Lausanne
Zolt??n KutalikUniversity of Lausanne
Zolt??n Kutalik
Zolt??n KutalikCenter for Primary Care and Public Health (Unisante), University of Lausanne
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