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Accession: PRJNA766172 ID: 766172

Homo sapiens (human)

Sanger sequences and qPCR data for human samples used in the study of UPIP-qPCR.

See Genome Information for Homo sapiens
The detection and identification of single nucleotide polymorphism (SNP) is essential for determining patient disease susceptibility and the delivery of medicines targeted to the individual. More...
AccessionPRJNA766172
Data TypeRaw sequence reads, Other
ScopeMonoisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
Grants
  • "The study of cardiovascular disease" (Grant ID 31430041, National Natural Science Foundation of China)
  • "Mechanism of noncoding RNA in cardiovascular disease" (Grant ID 91849209, Major Research Program of the National Natural Science Foundation of China)
  • "Universal probe-based intermediate primer-triggered qPCR (UPIP-qPCR) for SNP genotyping" (Grant ID 2018M632613, China Postdoctoral Science Foundation)
SubmissionRegistration date: 25-Sep-2021
Weifang Medical University
RelevanceMedical
Locus Tag PrefixLC818
Project Data:
Resource NameNumber
of Links
BioSample1
No public data is linked to this project. Any recently released data that cites this project will be linked to it within a few days.

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    Sanger sequences and qPCR data for human samples used in the study of UPIP-qPCR.
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