Improving SNP discovery by base alignment quality. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Inference of human population history from individual whole-genome sequences. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
pIRS: Profile-based Illumina pair-end reads simulator. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Exploring single-sample SNP and INDEL calling with whole-genome de novo assembly. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Extremely low-coverage sequencing and imputation increases power for genome-wide association studies. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
A direct characterization of human mutation based on microsatellites. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
A high-coverage genome sequence from an archaic Denisovan individual. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
SOAPindel: efficient identification of indels from short paired reads. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
The date of interbreeding between Neandertals and modern humans. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
