TY - JOUR
T1 - I am hiQ—a novel pair of accuracy indices for imputed genotypes
AU - Rosenberger, Albert
AU - Tozzi, Viola
AU - Bickeböller, Heike
AU - Hung, Rayjean J.
AU - Christiani, David C.
AU - Caporaso, Neil E.
AU - Liu, Geoffrey
AU - Le Marchand, Loic
AU - Albanes, Demetrios
AU - Aldrich, Melinda C.
AU - Tardon, Adonina
AU - Fernández-Tardón, Guillermo
AU - Rennert, Gad
AU - Field, John K.
AU - Davies, Mike
AU - Liloglou, Triantafillos
AU - Kiemeney, Lambertus A.
AU - Lazarus, Philip
AU - Haugen, Aage
AU - Zienolddiny, Shanbeh
AU - Lam, Stephen
AU - Schabath, Matthew B.
AU - Andrew, Angeline S.
AU - Duell, Eric J.
AU - Arnold, Susanne M.
AU - Brunnström, Hans
AU - Melander, Olle
AU - Goodman, Gary E.
AU - Chen, Chu
AU - Doherty, Jennifer A.
AU - Teare, Marion Dawn
AU - Cox, Angela
AU - Woll, Penella J.
AU - Risch, Angela
AU - Muley, Thomas R.
AU - Johansson, Mikael
AU - Brennan, Paul
AU - Landi, Maria Teresa
AU - Shete, Sanjay S.
AU - Amos, Christopher I.
AU - The INTEGRAL-ILCCO Consortium
A2 - Bojesen, Stig E.
N1 - Publisher Copyright:
© 2022, The Author(s).
PY - 2022/12
Y1 - 2022/12
N2 - Background: Imputation of untyped markers is a standard tool in genome-wide association studies to close the gap between directly genotyped and other known DNA variants. However, high accuracy with which genotypes are imputed is fundamental. Several accuracy measures have been proposed and some are implemented in imputation software, unfortunately diversely across platforms. In the present paper, we introduce Iam hiQ, an independent pair of accuracy measures that can be applied to dosage files, the output of all imputation software. Iam (imputation accuracy measure) quantifies the average amount of individual-specific versus population-specific genotype information in a linear manner. hiQ (heterogeneity in quantities of dosages) addresses the inter-individual heterogeneity between dosages of a marker across the sample at hand. Results: Applying both measures to a large case–control sample of the International Lung Cancer Consortium (ILCCO), comprising 27,065 individuals, we found meaningful thresholds for Iam and hiQ suitable to classify markers of poor accuracy. We demonstrate how Manhattan-like plots and moving averages of Iam and hiQ can be useful to identify regions enriched with less accurate imputed markers, whereas these regions would by missed when applying the accuracy measure info (implemented in IMPUTE2). Conclusion: We recommend using Iam hiQ additional to other accuracy scores for variant filtering before stepping into the analysis of imputed GWAS data.
AB - Background: Imputation of untyped markers is a standard tool in genome-wide association studies to close the gap between directly genotyped and other known DNA variants. However, high accuracy with which genotypes are imputed is fundamental. Several accuracy measures have been proposed and some are implemented in imputation software, unfortunately diversely across platforms. In the present paper, we introduce Iam hiQ, an independent pair of accuracy measures that can be applied to dosage files, the output of all imputation software. Iam (imputation accuracy measure) quantifies the average amount of individual-specific versus population-specific genotype information in a linear manner. hiQ (heterogeneity in quantities of dosages) addresses the inter-individual heterogeneity between dosages of a marker across the sample at hand. Results: Applying both measures to a large case–control sample of the International Lung Cancer Consortium (ILCCO), comprising 27,065 individuals, we found meaningful thresholds for Iam and hiQ suitable to classify markers of poor accuracy. We demonstrate how Manhattan-like plots and moving averages of Iam and hiQ can be useful to identify regions enriched with less accurate imputed markers, whereas these regions would by missed when applying the accuracy measure info (implemented in IMPUTE2). Conclusion: We recommend using Iam hiQ additional to other accuracy scores for variant filtering before stepping into the analysis of imputed GWAS data.
KW - Accuracy measures
KW - Genotype imputation
KW - GWAS
KW - High-throughput genotyping
UR - http://www.scopus.com/inward/record.url?scp=85123801091&partnerID=8YFLogxK
U2 - 10.1186/s12859-022-04568-3
DO - 10.1186/s12859-022-04568-3
M3 - Journal article
C2 - 35073846
AN - SCOPUS:85123801091
SN - 1471-2105
VL - 23
JO - BMC Bioinformatics
JF - BMC Bioinformatics
IS - 1
M1 - 50
ER -