Benjamin Michael Neale, Ph.D.
This page shows the publications co-authored by Benjamin Neale and Heng Li.
A synthetic-diploid benchmark for accurate variant-calling evaluation. Nat Methods. 2018 08; 15(8):595-597.
Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects. Nat Commun. 2018 10 02; 9(1):4038.
Extremely low-coverage sequencing and imputation increases power for genome-wide association studies. Nat Genet. 2012 May 20; 44(6):631-5.
The connection strength for co-authors is the sum of the scores for each of their shared publications.
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