Lista de obras -

A copy number variant is associated with a spectrum of pigmentation patterns in the rock pigeon (Columba livia)

scientific article published on 20 May 2020

A spectrum of free software tools for processing the VCF variant call format: vcflib, bio-vcf, cyvcf2, hts-nim and slivar

artículo científico publicado en 2022

Adaptive archaic introgression of copy number variants and the discovery of previously unknown human genes

scientific article published on 01 October 2019

Antimicrobial Functions of Lactoferrin Promote Genetic Conflicts in Ancient Primates and Modern Humans

artículo científico publicado en 2016

Chromosome-level genome assembly of <i>Mentha longifolia</i> L. reveals gene organization underlying disease resistance and essential oil traits

artículo científico publicado en 2022

Comparative Annotation Toolkit (CAT) - simultaneous clade and personal genome annotation

article published in 2017

Comparative Annotation Toolkit (CAT)-simultaneous clade and personal genome annotation

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

artículo científico publicado en 2018

De novo genic mutations among a Chinese autism spectrum disorder cohort.

artículo científico publicado en 2016

DisAp-dependent striated fiber elongation is required to organize ciliary arrays.

artículo científico publicado en 2014

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

artículo científico publicado en 2016

Epistatic and combinatorial effects of pigmentary gene mutations in the domestic pigeon

artículo científico publicado en 2014

Extended haplotype-phasing of long-read de novo genome assemblies using Hi-C

artículo científico publicado en 2021

Genomic Patterns of De Novo Mutation in Simplex Autism.

artículo científico publicado en 2017

Haplotype-resolved genomes provide insights into structural variation and gene content in Angus and Brahman cattle

artículo científico publicado en 2020

High-resolution comparative analysis of great ape genomes

artículo científico publicado en 2018

Improved assembly and variant detection of a haploid human genome using single-molecule, high-fidelity long reads

scientific article published on 11 November 2019

Interchromosomal core duplicons drive both evolutionary instability and disease susceptibility of the Chromosome 8p23.1 region

artículo científico publicado en 2016

Long-read assembly of the Chinese rhesus macaque genome and identification of ape-specific structural variants

artículo científico publicado en 2019

Long-read sequence assembly of the gorilla genome

artículo científico publicado en 2016

Multi-platform discovery of haplotype-resolved structural variation in human genomes

artículo científico publicado en 2019

Wham: Identifying Structural Variants of Biological Consequence

artículo científico publicado en 2015

Lista de obras de

A copy number variant is associated with a spectrum of pigmentation patterns in the rock pigeon (Columba livia)

A spectrum of free software tools for processing the VCF variant call format: vcflib, bio-vcf, cyvcf2, hts-nim and slivar

Adaptive archaic introgression of copy number variants and the discovery of previously unknown human genes

Antimicrobial Functions of Lactoferrin Promote Genetic Conflicts in Ancient Primates and Modern Humans

Chromosome-level genome assembly of <i>Mentha longifolia</i> L. reveals gene organization underlying disease resistance and essential oil traits

Comparative Annotation Toolkit (CAT) - simultaneous clade and personal genome annotation

Comparative Annotation Toolkit (CAT)-simultaneous clade and personal genome annotation

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

De novo genic mutations among a Chinese autism spectrum disorder cohort.

DisAp-dependent striated fiber elongation is required to organize ciliary arrays.

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

Epistatic and combinatorial effects of pigmentary gene mutations in the domestic pigeon

Extended haplotype-phasing of long-read de novo genome assemblies using Hi-C

Genomic Patterns of De Novo Mutation in Simplex Autism.

Haplotype-resolved genomes provide insights into structural variation and gene content in Angus and Brahman cattle

High-resolution comparative analysis of great ape genomes

Improved assembly and variant detection of a haploid human genome using single-molecule, high-fidelity long reads

Interchromosomal core duplicons drive both evolutionary instability and disease susceptibility of the Chromosome 8p23.1 region

Long-read assembly of the Chinese rhesus macaque genome and identification of ape-specific structural variants

Long-read sequence assembly of the gorilla genome

Multi-platform discovery of haplotype-resolved structural variation in human genomes

Wham: Identifying Structural Variants of Biological Consequence