MBV: a method to solve sample mislabeling and detect technical bias in large combined genotype and sequencing assay datasets

MOTIVATION: Large genomic datasets combining genotype and sequence data, such as for expression quantitative trait loci (eQTL) detection, require perfect matching between both data types. RESULTS: We described here MBV (Match BAM to VCF); a method to quickly solve sample mislabeling and detect cross...

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Bibliografiset tiedot
Julkaisussa:Bioinformatics
Päätekijät: Fort, Alexandre, Panousis, Nikolaos I, Garieri, Marco, Antonarakis, Stylianos E, Lappalainen, Tuuli, Dermitzakis, Emmanouil T, Delaneau, Olivier
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Oxford University Press 2017
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Applications Notes
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6044394/
https://ncbi.nlm.nih.gov/pubmed/28186259
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btx074
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