Structural variants are implicated in numerous diseases and make up the majority of varying
nucleotides among human genomes. Here we describe an integrated set of eight structural …

The incomplete identification of structural variants (SVs) from whole-genome sequencing
data limits studies of human genetic diversity and disease association. Here, we apply a suite …

We report the sequences of 1,244 human Y chromosomes randomly ascertained from 26
worldwide populations by the 1000 Genomes Project. We discovered more than 65,000 …

The 1000 Genomes Project was launched as one of the largest distributed data collection
and analysis projects ever undertaken in biology. In addition to the primary scientific goals of …

The International Genome Sample Resource (IGSR; http://www.internationalgenome.org )
expands in data type and population diversity the resources from the 1000 Genomes Project. …

Background Rare coding variants constitute an important class of human genetic variation,
but are underrepresented in current databases that are based on small population samples. …

Background It is widely accepted that orthologous genes between species are conserved at
the sequence level and perform similar functions in different organisms. However, the level …

We present a set of biallelic SNVs and INDELs, from 2,548 samples spanning 26 populations
from the 1000 Genomes Project, called de novo on GRCh38. We believe this will be a …

The 1000 Genomes Project produced more than 100 trillion basepairs of short read sequence
from more than 2600 samples in 26 populations over a period of five years. In its final …

… Xiangqun Zheng-Bradley … Xiangqun Zheng-Bradley was a member of the 1000 Genomes
Data Coordination Centre and currently works on the International Genome Sample Resource. …