دورية أكاديمية

Allele balance bias identifies systematic genotyping errors and false disease associations.

التفاصيل البيبلوغرافية
العنوان: Allele balance bias identifies systematic genotyping errors and false disease associations.
المؤلفون: Muyas, F, Bosio, M, Puig, A, Susak, H, Domènech, L, Escaramis, G, Zapata, L, Demidov, G, Estivill, X, Rabionet, R, Ossowski, S
المساهمون: Zapata Ortiz, Luis
بيانات النشر: WILEY
سنة النشر: 2023
المجموعة: The Institute of Cancer Research (ICR): Publications Repository
مصطلحات موضوعية: allele balance, false positive variant calls, genetic variant detection, systematic NGS errors, Alleles, Bias, Databases, Genetic, Disease, Genetic Association Studies, Genome, Human, Genotype, Genotyping Techniques, Humans, Models, Polymorphism, Single Nucleotide
جغرافية الموضوع: United States
الوصف: In recent years, next-generation sequencing (NGS) has become a cornerstone of clinical genetics and diagnostics. Many clinical applications require high precision, especially if rare events such as somatic mutations in cancer or genetic variants causing rare diseases need to be identified. Although random sequencing errors can be modeled statistically and deep sequencing minimizes their impact, systematic errors remain a problem even at high depth of coverage. Understanding their source is crucial to increase precision of clinical NGS applications. In this work, we studied the relation between recurrent biases in allele balance (AB), systematic errors, and false positive variant calls across a large cohort of human samples analyzed by whole exome sequencing (WES). We have modeled the AB distribution for biallelic genotypes in 987 WES samples in order to identify positions recurrently deviating significantly from the expectation, a phenomenon we termed allele balance bias (ABB). Furthermore, we have developed a genotype callability score based on ABB for all positions of the human exome, which detects false positive variant calls that passed state-of-the-art filters. Finally, we demonstrate the use of ABB for detection of false associations proposed by rare variant association studies. Availability: https://github.com/Francesc-Muyas/ABBTest.
نوع الوثيقة: article in journal/newspaper
وصف الملف: Print-Electronic; 126; application/pdf
اللغة: English
تدمد: 1059-7794
1098-1004
العلاقة: Human Mutation, 2019, 40 (1), pp. 115 - 126; https://repository.icr.ac.uk/handle/internal/5875Test
DOI: 10.1002/humu.23674
الإتاحة: https://doi.org/10.1002/humu.23674Test
https://repository.icr.ac.uk/handle/internal/5875Test
حقوق: http://creativecommons.org/licenses/by/4.0Test/
رقم الانضمام: edsbas.A1EFDCF
قاعدة البيانات: BASE
الوصف
تدمد:10597794
10981004
DOI:10.1002/humu.23674