Erratum to: Hum Genet (2014) 133:1199–1215 DOI 10.1007/s00439-014-1476-7, Hum Genet (2014) 133:1331–1341 DOI 10.1007/s00439-014-1479-4, Hum Genet (2015) 134:3–11 DOI 10.1007/s00439-014-1482-9
The following three articles are part of the special issue on “Computational Molecular Medicine”, but have accidently already been published in previous issues. Furthermore, the special topic title “Computational Molecular Medicine” was missed to include in those articles.
Missing heritability of common diseases and treatments outside the protein-coding exome
Wolfgang Sadee · Katherine Hartmann · Michał Seweryn · Maciej Pietrzak · Samuel K. Handelman · Grzegorz A. Rempala
10.1007/s00439-014-1476-7 (Volume 133, Issue 10)
Using familial information for variant filtering in high-throughput sequencing studies
Melanie Bahlo · Rick Tankard · Vesna Lukic · Karen L. Oliver · Katherine R. Smith
10.1007/s00439-014-1479-4 (Volume 133, Issue 11)
Using drug response data to identify molecular effectors, and molecular “omic” data to identify candidate drugs in cancer
William C. Reinhold · Sudhir Varma · Vinodh N. Rajapakse · Augustin Luna · Fabricio Garmus Sousa · Kurt W. Kohn · Yves G. Pommier
10.1007/s00439-014-1482-9 (Volume 134, Issue 1)
Footnotes
The online version of the original articles can be found under doi:10.1007/s00439-014-1476-7, 10.1007/s00439-014-1479-4 and 10.1007/s00439-014-1482-9.