PT  - JOURNAL ARTICLE
AU  - Asif Javed
AU  - Saloni Agrawal
AU  - Pauline C. Ng
TI  - Phen-Gen: Combining Phenotype and Genotype to Analyze Rare Disorders
AID  - 10.1101/015727
DP  - 2015 Jan 01
TA  - bioRxiv
PG  - 015727
4099  - http://biorxiv.org/content/early/2015/02/26/015727.short
4100  - http://biorxiv.org/content/early/2015/02/26/015727.full
AB  - We introduce Phen-Gen, a method which combines patient’s disease symptoms and sequencing data with prior domain knowledge to identify the causative gene(s) for rare disorders. Simulations reveal that the causal variant is ranked first in 88% cases when it is coding; which is 52% advantage over a genotype-only approach and outperforms existing methods by 13-58%. If disease etiology is unknown, the causal variant is assigned top-rank in 71% of simulations.