TY  - RPRT
TI  - Identification and prioritisation of causal variants in human genetic disorders from exome or whole genome sequencing data
AU  - Paramasivam, N.
AU  - Granzow, M.
AU  - Evers, C.
AU  - Hinderhofer, K.
AU  - Wiemann, S.
AU  - Bartram, C. R.
AU  - Eils, R.
AU  - Schlesner, M.
PY  - 2017
DO  - 10.1101/209882
UR  - https://www.biorxiv.org/content/10.1101/209882v1
ID  - 10.1101/209882
ER  -