Literature DB >> 21734406

Evaluating the influence of quality control decisions and software algorithms on SNP calling for the affymetrix 6.0 SNP array platform.

Mariza de Andrade1, Elizabeth J Atkinson, William R Bamlet, Martha E Matsumoto, Sooraj Maharjan, Susan L Slager, Celine M Vachon, Julie M Cunningham, Sharon L R Kardia.   

Abstract

OBJECTIVE: Our goal was to evaluate the influence of quality control (QC) decisions using two genotype calling algorithms, CRLMM and Birdseed, designed for the Affymetrix SNP Array 6.0.
METHODS: Various QC options were tried using the two algorithms and comparisons were made on subject and call rate and on association results using two data sets.
RESULTS: For Birdseed, we recommend using the contrast QC instead of QC call rate for sample QC. For CRLMM, we recommend using the signal-to-noise rate ≥4 for sample QC and a posterior probability of 90% for genotype accuracy. For both algorithms, we recommend calling the genotype separately for each plate, and dropping SNPs with a lower call rate (<95%) before evaluating samples with lower call rates. To investigate whether the genotype calls from the two algorithms impacted the genome-wide association results, we performed association analysis using data from the GENOA cohort; we observed that the number of significant SNPs were similar using either CRLMM or Birdseed.
CONCLUSIONS: Using our suggested workflow both algorithms performed similarly; however, fewer samples were removed and CRLMM took half the time to run our 854 study samples (4.2 h) compared to Birdseed (8.4 h).
Copyright © 2011 S. Karger AG, Basel.

Mesh:

Year:  2011        PMID: 21734406      PMCID: PMC3136375          DOI: 10.1159/000328843

Source DB:  PubMed          Journal:  Hum Hered        ISSN: 0001-5652            Impact factor:   0.444


  11 in total

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Authors: 
Journal:  Hypertension       Date:  2002-01       Impact factor: 10.190

2.  Spoiling the whole bunch: quality control aimed at preserving the integrity of high-throughput genotyping.

Authors:  Anna Pluzhnikov; Jennifer E Below; Anuar Konkashbaev; Anna Tikhomirov; Emily Kistner-Griffin; Cheryl A Roe; Dan L Nicolae; Nancy J Cox
Journal:  Am J Hum Genet       Date:  2010-07-09       Impact factor: 11.025

3.  A genotype calling algorithm for affymetrix SNP arrays.

Authors:  Nusrat Rabbee; Terence P Speed
Journal:  Bioinformatics       Date:  2005-11-02       Impact factor: 6.937

4.  Exploration, normalization, and genotype calls of high-density oligonucleotide SNP array data.

Authors:  Benilton Carvalho; Henrik Bengtsson; Terence P Speed; Rafael A Irizarry
Journal:  Biostatistics       Date:  2006-12-22       Impact factor: 5.899

Review 5.  Biostatistical aspects of genome-wide association studies.

Authors:  Andreas Ziegler; Inke R König; John R Thompson
Journal:  Biom J       Date:  2008-02       Impact factor: 2.207

6.  PLINK: a tool set for whole-genome association and population-based linkage analyses.

Authors:  Shaun Purcell; Benjamin Neale; Kathe Todd-Brown; Lori Thomas; Manuel A R Ferreira; David Bender; Julian Maller; Pamela Sklar; Paul I W de Bakker; Mark J Daly; Pak C Sham
Journal:  Am J Hum Genet       Date:  2007-07-25       Impact factor: 11.025

7.  Quality control procedures for genome-wide association studies.

Authors:  Stephen Turner; Loren L Armstrong; Yuki Bradford; Christopher S Carlson; Dana C Crawford; Andrew T Crenshaw; Mariza de Andrade; Kimberly F Doheny; Jonathan L Haines; Geoffrey Hayes; Gail Jarvik; Lan Jiang; Iftikhar J Kullo; Rongling Li; Hua Ling; Teri A Manolio; Martha Matsumoto; Catherine A McCarty; Andrew N McDavid; Daniel B Mirel; Justin E Paschall; Elizabeth W Pugh; Luke V Rasmussen; Russell A Wilke; Rebecca L Zuvich; Marylyn D Ritchie
Journal:  Curr Protoc Hum Genet       Date:  2011-01

8.  Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL.

Authors:  Susan L Slager; Kari G Rabe; Sara J Achenbach; Celine M Vachon; Lynn R Goldin; Sara S Strom; Mark C Lanasa; Logan G Spector; Laura Z Rassenti; Jose F Leis; Nicola J Camp; Martha Glenn; Neil E Kay; Julie M Cunningham; Curtis A Hanson; Gerald E Marti; J Brice Weinberg; Vicki A Morrison; Brian K Link; Timothy G Call; Neil E Caporaso; James R Cerhan
Journal:  Blood       Date:  2010-12-03       Impact factor: 22.113

Review 9.  Genotype imputation.

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Journal:  Annu Rev Genomics Hum Genet       Date:  2009       Impact factor: 8.929

10.  Validation and extension of an empirical Bayes method for SNP calling on Affymetrix microarrays.

Authors:  Shin Lin; Benilton Carvalho; David J Cutler; Dan E Arking; Aravinda Chakravarti; Rafael A Irizarry
Journal:  Genome Biol       Date:  2008-04-03       Impact factor: 13.583

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  4 in total

1.  Rare autosomal copy number variations in early-onset familial Alzheimer's disease.

Authors:  B V Hooli; Z M Kovacs-Vajna; K Mullin; M A Blumenthal; M Mattheisen; C Zhang; C Lange; G Mohapatra; L Bertram; R E Tanzi
Journal:  Mol Psychiatry       Date:  2013-06-11       Impact factor: 15.992

2.  Comprehensive Analysis of Genome Rearrangements in Eight Human Malignant Tumor Tissues.

Authors:  Stefanie Marczok; Birgit Bortz; Chong Wang; Heike Pospisil
Journal:  PLoS One       Date:  2016-07-08       Impact factor: 3.240

Review 3.  Use of single nucleotide polymorphism array technology to improve the identification of chromosomal lesions in leukemia.

Authors:  Ilaria Iacobucci; Annalisa Lonetti; Cristina Papayannidis; Giovanni Martinelli
Journal:  Curr Cancer Drug Targets       Date:  2013-09       Impact factor: 3.428

4.  Family-based association analyses of imputed genotypes reveal genome-wide significant association of Alzheimer's disease with OSBPL6, PTPRG, and PDCL3.

Authors:  C Herold; B V Hooli; K Mullin; T Liu; J T Roehr; M Mattheisen; A R Parrado; L Bertram; C Lange; R E Tanzi
Journal:  Mol Psychiatry       Date:  2016-02-02       Impact factor: 15.992

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