Impact of variant-level batch effects on identification of genetic risk factors in large sequencing studies

Genetic studies have shifted to sequencing-based rare variants discovery after decades of success in identifying common disease variants by Genome-Wide Association Studies using Single Nucleotide Polymorphism chips. Sequencing-based studies require large sample sizes for statistical power and theref...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:PLoS One
Egile Nagusiak: Wickland, Daniel P., Ren, Yingxue, Sinnwell, Jason P., Reddy, Joseph S., Pottier, Cyril, Sarangi, Vivekananda, Carrasquillo, Minerva M., Ross, Owen A., Younkin, Steven G., Ertekin-Taner, Nilüfer, Rademakers, Rosa, Hudson, Matthew E., Mainzer, Liudmila Sergeevna, Biernacka, Joanna M., Asmann, Yan W.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Public Library of Science 2021
Gaiak:
Research Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC8051815/
https://ncbi.nlm.nih.gov/pubmed/33861770
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0249305
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