Table 1.
Acronyms used in this review
Abbreviation | Definition |
---|---|
1KGP | 1000 Genomes Project |
AFR | African ancestry |
AMR | American ancestry |
BNG | Bionanogenomics |
bp | basepair |
CNV | copy-number variant |
DAVID | Database for Annotation, Visualization and Integrated Discovery |
EAS | East asian ancestry |
EUR | European ancestry |
eQTL | expression quantitative trait locus |
FST | fixation index |
gnomAD | Genome Aggregation Database |
GoNL | Genome of the Netherlands |
GTEx | Genotype-Tissue Expression |
hESC | human embryonic stem cells |
HGSVC | Human Genome Structural Variation Consortium |
Hi-C or HIC | high-throughout chromatin conformation capture |
HiFi | high fidelity |
HPRC | Human Pangenome Reference Consortium |
HSD | human-specific segmental duplication |
HSE | human-specific expansion |
i2QTL | Integrated iPSC QTL |
IGC | interlocus gene conversion |
IL | Illumina |
iPSC | induced Pluripotent Stem Cell |
kbp | kilobasepairs |
kya | thousand years ago |
LD | linkage disequilibrium |
LRS | long-read sequencing |
Mbp | megabasepairs |
mCNV | multiple (multiallelic) copy-number variant |
MESA | Multi-Ethnic Study of Atherosclerosis |
mya | million years ago |
NAHR | non-allelic homologous recombination |
NHEJ | non-homologous end-joining |
ONT | Oxford Nanopore Technologies |
PacBio or PB | Pacific Biosciences |
PSVs | paralog-specific variants |
SAS | South Asian ancestry |
SD | segmental duplication |
SINE | short interspersed nuclear element |
SNV | single-nucleotide variant |
SRS | short-read sequencing |
SV | structural variant |
SVA | SINE-R-VNTR-Alu |
T2T | Telomore-to-Telomere |
TAD | topologically-associated domain |