TY  - RPRT
TI  - Matching whole genomes to rare genetic disorders: Identification of potential causative variants using phenotype-weighted knowledge in the CAGI SickKids5 clinical genomes challenge
AU  - Pal, L. R.
AU  - Kundu, K.
AU  - Yin, Y.
AU  - Moult, J.
PY  - 2019
DO  - 10.1101/707687
UR  - https://www.biorxiv.org/content/10.1101/707687v1
ID  - 10.1101/707687
ER  -