Patch, Ann-Marie <br/><br/>
Germline and somatic variant identification using BGISEQ-500 and HiSeq X Ten whole genome sequencing.  [electronic resource] 

 -  PloS one  2018 
 - e0190264 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1932-6203 
<br/><br/><label>Standard No.: </label>10.1371/journal.pone.0190264  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Genome, Human<br/>Germ Cells<br/>High-Throughput Nucleotide Sequencing--methods<br/>Humans<br/>INDEL Mutation<br/>Polymorphism, Single Nucleotide