Cite
APA Citation
Humble, E., Thorne, M., Forcada, J., & Hoffman, J. (2016). transcriptomic SNP discovery for custom genotyping arrays: impacts of sequence data, SNP calling method and genotyping technology on the probability of validation success. BMC research notes, 9, 1–12. http://access.bl.uk/ark:/81055/vdc_100080657499.0x000033