Comparing strategies for combined testing of rare and common variants in whole sequence and genome-wide genotype data. Malzahn, D., Friedrichs, S., & Bickeb"oller, H. BMC Proceedings, 2016. Paper doi bibtex @article{Malzahn2016Comparing,
abstract = {},
author = {Malzahn, D{\"o}rthe and Friedrichs, Stefanie and Bickeb{\"o}ller, Heike},
year = {2016},
title = {{Comparing strategies for combined testing of rare and common variants in whole sequence and genome-wide genotype data}},
url = {http://dx.doi.org/10.1186/s12919-016-0042-9},
keywords = {gen;phd},
volume = {10},
number = {S7},
issn = {1753-6561},
journal = {{BMC Proceedings}},
doi = {10.1186/s12919-016-0042-9},
howpublished = {refereed}
}
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