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Transcriptomic SNP discovery for custom genotyping arrays: impacts of sequence data, SNP calling method and genotyping technology on the probability of validation success

Crossref DOI link: https://doi.org/10.1186/s13104-016-2209-x

Published Online: 2016-08-26

Published Print: 2016-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Humble, Emily http://orcid.org/0000-0001-6841-1269
Thorne, Michael A. S.

Forcada, Jaume

Hoffman, Joseph I.
Funding

Funding for this research was provided by:

Deutsche Forschungsgemeinschaft (HO 5122/3-1)

Marie Curie FP7 Reintegration Grant (PCIG-GA-2011-303618)
License Information

Text and Data Mining valid from 2016-08-26

Version of Record valid from 2016-08-26
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Article History

Received: 31 March 2016

Accepted: 6 August 2016

First Online: 26 August 2016

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