Error-tolerant EST database searches by tandem mass spectrometry and multiTag software. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Medical sequencing at the extremes of human body mass. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Most rare missense alleles are deleterious in humans: implications for complex disease and association studies. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Toxicity of influenza A virus matrix protein 2 for mammalian cells is associated with its intrinsic proton-channeling activity. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Sequence similarity-driven proteomics in organisms with unknown genomes by LC-MS/MS and automated de novo sequencing. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Widely distributed noncoding purifying selection in the human genome. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Analysis of sequence conservation at nucleotide resolution. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Large-scale identification and evolution indexing of tyrosine phosphorylation sites from murine brain. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Common single-nucleotide polymorphisms act in concert to affect plasma levels of high-density lipoprotein cholesterol. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
