Wellcome Trust Sanger Institute
18 papers found
Whole-genome view of the consequences of a population bottleneck using 2926 genome sequences from Finland and United Kingdom
Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps
A global reference for human genetic variation
An integrated map of structural variation in 2,504 human genomes.
Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformations.
Estimating Genome-Wide Significance for Whole-Genome Sequencing Studies: Genome-Wide Significance for Rare Variants
An atlas of genetic influences on human blood metabolites.
An integrated map of genetic variation from 1,092 human genomes
Multiple de novo copy number variations in two subjects with developmental problems and multiple congenital anomalies
Mapping copy number variation by population scale genome sequencing
A map of human genome variation from population-scale sequencing
Origins and functional impact of copy number variation in the human genome
Deep short-read sequencing of chromosome 17 from the mouse strains A/J and CAST/Ei identifies significant germline variation and candidate genes that regulate liver triglyceride levels
Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry
Characterisation of conserved non-coding sequences in vertebrate genomes using bioinformatics, statistics and functional studies
Striking nucleotide frequency pattern at the borders of highly conserved vertebrate non-coding sequences
Highly Conserved Non-Coding Sequences Are Associated with Vertebrate Development
Increases in Human T Helper 2 Cytokine Responses toSchistosoma mansoniWorm and Worm‐Tegument Antigens Are Induced by Treatment with Praziquantel
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