Epigenetic and evolutionary features of ape subterminal heterochromatin
- First Published October 22, 2025
An integrative TAD catalog in lymphoblastoid cell lines discloses the functional impact of deletions and insertions in human genomes
- First Published December 5, 2024
TBC1D3 gene family in humans" > Independent expansion, selection, and hypervariability of the TBC1D3 gene family in humans
- First Published August 6, 2024
Phased nanopore assembly with Shasta and modular graph phasing with GFAse
- First Published April 16, 2024
Whole-genome long-read sequencing downsampling and its effect on variant-calling precision and recall
- First Published December 7, 2023
Characterizing nucleotide variation and expansion dynamics in human-specific variable number tandem repeats
- First Published July 9, 2021
Single-cell strand sequencing of a macaque genome reveals multiple nested inversions and breakpoint reuse during primate evolution
- First Published October 22, 2020
HiCanu: accurate assembly of segmental duplications, satellites, and allelic variants from high-fidelity long reads
- First Published August 14, 2020
Transcriptional fates of human-specific segmental duplications in brain
- First Published September 18, 2018
Comparative Annotation Toolkit (CAT)—simultaneous clade and personal genome annotation
- First Published June 8, 2018
Corrigendum: Discovery and genotyping of structural variation from long-read haploid genome sequence data
- First Published January 2, 2018
Corrigendum: The evolution of African great ape subtelomeric heterochromatin and the fusion of human chromosome 2
- First Published September 1, 2017
Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly
- First Published April 10, 2017
Discovery and genotyping of structural variation from long-read haploid genome sequence data
- First Published November 28, 2016
Interchromosomal core duplicons drive both evolutionary instability and disease susceptibility of the Chromosome 8p23.1 region
- First Published October 7, 2016
Corrigendum: MIPSTR: a method for multiplex genotyping of germline and somatic STR variation across many individuals
- First Published August 3, 2015
MIPSTR: a method for multiplex genotyping of germline and somatic STR variation across many individuals
- First Published February 6, 2015
The discovery of integrated gene networks for autism and related disorders
- First Published November 5, 2014
Single haplotype assembly of the human genome from a hydatidiform mole
- First Published November 4, 2014
Reconstructing complex regions of genomes using long-read sequencing technology
- First Published January 13, 2014
Hominoid fission of chromosome 14/15 and the role of segmental duplications
- First Published September 27, 2013
Evolution and diversity of copy number variation in the great ape lineage
- First Published July 3, 2013
LRRC37 gene family" > Evolutionary dynamism of the primate LRRC37 gene family
- First Published October 11, 2012
Copy number variation detection and genotyping from exome sequence data
- First Published May 14, 2012
The evolution of African great ape subtelomeric heterochromatin and the fusion of human chromosome 2
- First Published March 14, 2012
Copy number variation of individual cattle genomes using next-generation sequencing
- First Published February 2, 2012
Simultaneous structural variation discovery among multiple paired-end sequenced genomes
- First Published November 2, 2011
Copy number variation analysis in the great apes reveals species-specific patterns of structural variation
- First Published August 8, 2011
Gorilla genome structural variation reveals evolutionary parallelisms with chimpanzee
- First Published June 17, 2011
Alu repeat discovery and characterization within human genomes" > Alu repeat discovery and characterization within human genomes
- First Published December 3, 2010
Genome-wide characterization of centromeric satellites from multiple mammalian genomes
- First Published November 16, 2010
A method for rapid, targeted CNV genotyping identifies rare variants associated with neurocognitive disease
- First Published June 8, 2009
Combinatorial algorithms for structural variation detection in high-throughput sequenced genomes
- First Published May 15, 2009
Alu repeats in primate genomes" > Comparative analysis of Alu repeats in primate genomes
- First Published May 1, 2009
The genomic architecture of segmental duplications and associated copy number variants in dogs
- First Published January 7, 2009
Sequencing human–gibbon breakpoints of synteny reveals mosaic new insertions at rearrangement sites
- First Published November 24, 2008
