Francioli, Laurent C <br/><br/>
A framework for the detection of de novo mutations in family-based sequencing data.  [electronic resource] 

 -  European journal of human genetics : EJHG  02 2017 
 - 227-233 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1476-5438 
<br/><br/><label>Standard No.: </label>10.1038/ejhg.2016.147  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Child<br/>Chromosomes, Human, X--genetics<br/>Exome<br/>Female<br/>Genome-Wide Association Study--methods<br/>Genotype<br/>Germ-Line Mutation<br/>Humans<br/>Male<br/>Models, Genetic<br/>Pedigree<br/>Polymorphism, Single Nucleotide<br/>Sequence Analysis, DNA--methods<br/>Software