KRGDB
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The large-scale variant database of 1722 Koreans based on whole genome sequencing.
Description
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The large-scale variant database of 1722 Koreans based on whole genome sequencing.
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:28:30.609352
Webpage:
http://coda.nih.go.kr/coda/KRGDB/index.jspWebpage
More detailed information about this field from each metasource.
http://coda.nih.go.kr/coda/KRGDB/index.jsp
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:28:30.609352
Publications:
Publications
More detailed information about this field from each metasource.
KRGDB: the large-scale variant database of 1722 Koreans based on whole genome sequencing
PMID: 32133509
metasource: bio.tools
version: extracted_at: 2022-11-04T11:28:30.609352
Publications
More detailed information about this field from each metasource.
KRGDB: the large-scale variant database of 1722 Koreans based on whole genome sequencing
PMID: 32133509
metasource: bio.tools
version: extracted_at: 2022-11-04T11:28:30.609352
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KRGDB: the large-scale variant database of 1722 Koreans based on whole genome sequencing
PubMed citations: 11.
11 articles citing: KRGDB: the large-scale variant database of 1722 Koreans based on whole genome sequencing
Pathogenic NOTCH3 Variants Are Frequent Among the Korean General Population. PMID:34881353
Real-world data analysis of patients with cancer of unknown primary. PMID:34845302
Comparison of tumor mutation burden of 300 various non-Hodgkin lymphomas using panel based massively parallel sequencing. PMID:34461835
Genetic Polymorphisms of Pesticide-Metabolizing Enzymes and Transporters in Agricultural Workers and Thyroid Hormone Levels. PMID:34434063
New insights into hallux valgus by whole exome sequencing study. PMID:33926255
Analysis of BRCA1/2 variants of unknown significance in the prospective Korean Hereditary Breast Cancer study. PMID:33875706
Genetic variation analyses indicate conserved SARS-CoV-2-host interaction and varied genetic adaptation in immune response factors in modern human evolution. PMID:33595856
KCNV2-Associated Retinopathy: Genetics, Electrophysiology, and Clinical Course-KCNV2 Study Group Report 1. PMID:33309813
No association between SCN9A and monogenic human epilepsy disorders. PMID:33216760
A survey of genetic variants in SARS-CoV-2 interacting domains of ACE2, TMPRSS2 and TLR3/7/8 across populations. PMID:32858233
Exome Chip Analysis of 14,026 Koreans Reveals Known and Newly Discovered Genetic Loci Associated with Type 2 Diabetes Mellitus. PMID:32794382
Tags:
Tags
More detailed information about this field from each metasource.
gwas study
metasource: bio.tools
version: extracted_at: 2022-11-04T11:28:30.609352
genomics
metasource: bio.tools
version: extracted_at: 2022-11-04T11:28:30.609352
whole genome sequencing
metasource: bio.tools
version: extracted_at: 2022-11-04T11:28:30.609352
exome sequencing
metasource: bio.tools
version: extracted_at: 2022-11-04T11:28:30.609352
nutritional science
metasource: bio.tools
version: extracted_at: 2022-11-04T11:28:30.609352
Tags
More detailed information about this field from each metasource.
gwas study
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:28:30.609352
genomics
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:28:30.609352
whole genome sequencing
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:28:30.609352
exome sequencing
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:28:30.609352
nutritional science
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:28:30.609352
gwas study genomics whole genome sequencing exome sequencing nutritional science
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