Human mutation rate associated with DNA replication timing. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Multiplex padlock targeted sequencing reveals human hypermutable CpG variations. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Triplet repeat length bias and variation in the human transcriptome. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
A method and server for predicting damaging missense mutations. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Pooled association tests for rare variants in exon-resequencing studies. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Human allelic variation: perspective from protein function, structure, and evolution. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Development and validation of a computational method for assessment of missense variants in hypertrophic cardiomyopathy. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Assigning spectrum-specific P-values to protein identifications by mass spectrometry. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Progressive multifocal leukoencephalopathy (PML) development is associated with mutations in JC virus capsid protein VP1 that change its receptor specificity. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Computational and statistical approaches to analyzing variants identified by exome sequencing. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
