Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
A Bayesian deconvolution strategy for immunoprecipitation-based DNA methylome analysis. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Mapping short DNA sequencing reads and calling variants using mapping quality scores. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Accurate whole human genome sequencing using reversible terminator chemistry. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
The diploid genome sequence of an Asian individual. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
EnsemblCompara GeneTrees: Complete, duplication-aware phylogenetic trees in vertebrates. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Omics-based profiling of carcinoma of the breast and matched regional lymph node metastasis. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Haplotype frequencies in a sub-region of chromosome 19q13.3, related to risk and prognosis of cancer, differ dramatically between ethnic groups. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Fast and accurate short read alignment with Burrows-Wheeler transform. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Detecting SNPs and estimating allele frequencies in clonal bacterial populations by sequencing pooled DNA. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
