Lista de obras -

An Incomplete Understanding of Human Genetic Variation

artículo científico publicado en 2016

An integrated map of structural variation in 2,504 human genomes

artículo científico publicado en 2015

Augur: a bioinformatics toolkit for phylogenetic analyses of human pathogens

artículo científico publicado en 2021

Bovine NK-lysin: Copy number variation and functional diversification.

artículo científico publicado en 2015

Complete mapping of mutations to the SARS-CoV-2 spike receptor-binding domain that escape antibody recognition

scientific article published on 10 September 2020

Corrigendum: Discovery and genotyping of structural variation from long-read haploid genome sequence data

artículo científico publicado en 2018

Cryptic transmission of SARS-CoV-2 in Washington state

scientific article published on 10 September 2020

Discovery and genotyping of structural variation from long-read haploid genome sequence data.

artículo científico publicado en 2016

Emergence of a Homo sapiens-specific gene family and chromosome 16p11.2 CNV susceptibility

artículo científico publicado en 2016

Epigenetic origin of evolutionary novel centromeres

artículo científico publicado en 2017

Evolution and diversity of copy number variation in the great ape lineage

artículo científico publicado en 2013

Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA.

artículo científico publicado en 2015

Global diversity, population stratification, and selection of human copy-number variation

artículo científico publicado en 2015

Hominoid fission of chromosome 14/15 and the role of segmental duplications.

artículo científico publicado en 2013

Integrating genotypes and phenotypes improves long-term forecasts of seasonal influenza A/H3N2 evolution

scientific article published on 02 September 2020

Large Deletions at the SHOX Locus in the Pseudoautosomal Region Are Associated with Skeletal Atavism in Shetland Ponies

artículo científico publicado en 2016

Long-read sequence assembly of the gorilla genome

artículo científico publicado en 2016

Long-read sequencing and de novo assembly of a Chinese genome

artículo científico publicado en 2016

Rates and patterns of great ape retrotransposition

artículo científico publicado en 2013

Reconstructing complex regions of genomes using long-read sequencing technology

artículo científico publicado en 2014

Resolving the complexity of the human genome using single-molecule sequencing

artículo científico publicado en 2015

Single haplotype assembly of the human genome from a hydatidiform mole

artículo científico publicado en 2014

The birth of a human-specific neural gene by incomplete duplication and gene fusion

artículo científico publicado en 2017

denovo-db: a compendium of human de novo variants.

artículo científico publicado en 2016

Lista de obras de

An Incomplete Understanding of Human Genetic Variation

An integrated map of structural variation in 2,504 human genomes

Augur: a bioinformatics toolkit for phylogenetic analyses of human pathogens

Bovine NK-lysin: Copy number variation and functional diversification.

Complete mapping of mutations to the SARS-CoV-2 spike receptor-binding domain that escape antibody recognition

Corrigendum: Discovery and genotyping of structural variation from long-read haploid genome sequence data

Cryptic transmission of SARS-CoV-2 in Washington state

Discovery and genotyping of structural variation from long-read haploid genome sequence data.

Emergence of a Homo sapiens-specific gene family and chromosome 16p11.2 CNV susceptibility

Epigenetic origin of evolutionary novel centromeres

Evolution and diversity of copy number variation in the great ape lineage

Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA.

Global diversity, population stratification, and selection of human copy-number variation

Hominoid fission of chromosome 14/15 and the role of segmental duplications.

Integrating genotypes and phenotypes improves long-term forecasts of seasonal influenza A/H3N2 evolution

Large Deletions at the SHOX Locus in the Pseudoautosomal Region Are Associated with Skeletal Atavism in Shetland Ponies

Long-read sequence assembly of the gorilla genome

Long-read sequencing and de novo assembly of a Chinese genome

Rates and patterns of great ape retrotransposition

Reconstructing complex regions of genomes using long-read sequencing technology

Resolving the complexity of the human genome using single-molecule sequencing

Single haplotype assembly of the human genome from a hydatidiform mole

The birth of a human-specific neural gene by incomplete duplication and gene fusion

denovo-db: a compendium of human de novo variants.