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2022
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Estimating copy numbers of alleles from population-scale high-throughput sequencing data.
Not available
S-EPMC4331703
|
biostudies-literature
Cite
Distribution and effects of nonsense polymorphisms in human genes.
Not available
S-EPMC2561068
|
biostudies-literature
Cite
Japanese population structure, based on SNP genotypes from 7003 individuals compared to other ethnic groups: effects on population-based association studies.
Not available
S-EPMC2561928
|
biostudies-literature
Cite
HLA-VBSeq: accurate HLA typing at full resolution from whole-genome sequencing data.
Not available
S-EPMC4331721
|
biostudies-literature
Cite
Human immunodeficiency virus type 1 intergroup (M/O) recombination in cameroon.
Not available
S-EPMC112766
|
biostudies-literature
Cite
iJGVD: an integrative Japanese genome variation database based on whole-genome sequencing.
Not available
S-EPMC4785574
|
biostudies-literature
Cite
Integrated analysis of human genetic association study and mouse transcriptome suggests LBH and SHF genes as novel susceptible genes for amyloid-β accumulation in Alzheimer's disease.
Not available
S-EPMC6061045
|
biostudies-literature
Cite
Estimation of the carrier frequencies and proportions of potential patients by detecting causative gene variants associated with autosomal recessive bone dysplasia using a whole-genome reference panel of Japanese individuals.
Not available
S-EPMC7810679
|
biostudies-literature
Cite
Loss of CAPS2/Cadps2 leads to exocrine pancreatic cell injury and intracellular accumulation of secretory granules in mice.
Not available
S-EPMC9676974
|
biostudies-literature
Cite
Deciphering state-dependent immune features from multi-layer omics data at single-cell resolution.
Not available
S-EPMC12339405
|
biostudies-literature
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