Comparison among three variant callers and assessment of the accuracy of imputation from SNP array data to whole-genome sequence level in chicken

BACKGROUND: The technical progress in the last decade has made it possible to sequence millions of DNA reads in a relatively short time frame. Several variant callers based on different algorithms have emerged and have made it possible to extract single nucleotide polymorphisms (SNPs) out of the who...

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Pubblicato in:BMC Genomics
Autori principali: Ni, Guiyan, Strom, Tim M., Pausch, Hubert, Reimer, Christian, Preisinger, Rudolf, Simianer, Henner, Erbe, Malena
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2015
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Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4618161/
https://ncbi.nlm.nih.gov/pubmed/26486989
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-015-2059-2
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