Showing results 1 to 5 of 5
Title | Author(s) | Issue Date | |
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Assessment of aligner and SNP caller for next generation sequencing and a fast and accurate SNP detection method Proceeding/Conference:ISMB/ECCB 2013 Joint Conference | 2013 | ||
Deviation from baseline mutation burden provides powerful and robust rare-variants association test for complex diseases Journal:Nucleic Acids Research | 2022 | ||
2010 | |||
GWASdb: A database for human genetic variants identified by genome-wide association studies Journal:Nucleic Acids Research | 2012 | ||
2015 |