Related Experiment Video

Updated: Jul 7, 2025

Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry
05:53

Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry

Published on: June 21, 2018

10.2K

Genetic differentiation at probe SNPs leads to spurious results in meQTL discovery

Gillian L Meeks1, Brenna M Henn2,3, Shyamalika Gopalan4

  • 1Graduate Program in Integrative Genetics and Genomics, University of California Davis, Davis, CA, 95616, USA.

Communications Biology
|December 22, 2023
PubMed
Abstract

No abstract available in PubMed .

More Related Videos

Large-Scale Multi-Omics Genome-Wide Association Studies Mo-GWAS: Guidelines for Sample Preparation and Normalization
08:27

Large-Scale Multi-Omics Genome-Wide Association Studies Mo-GWAS: Guidelines for Sample Preparation and Normalization

Published on: July 27, 2021

3.7K
Screening for Functional Non-coding Genetic Variants Using Electrophoretic Mobility Shift Assay EMSA and DNA-affinity Precipitation Assay DAPA
11:35

Screening for Functional Non-coding Genetic Variants Using Electrophoretic Mobility Shift Assay EMSA and DNA-affinity Precipitation Assay DAPA

Published on: August 21, 2016

13.0K

Related Experiment Videos

Last Updated: Jul 7, 2025

Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry
05:53

Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry

Published on: June 21, 2018

10.2K
Large-Scale Multi-Omics Genome-Wide Association Studies Mo-GWAS: Guidelines for Sample Preparation and Normalization
08:27

Large-Scale Multi-Omics Genome-Wide Association Studies Mo-GWAS: Guidelines for Sample Preparation and Normalization

Published on: July 27, 2021

3.7K
Screening for Functional Non-coding Genetic Variants Using Electrophoretic Mobility Shift Assay EMSA and DNA-affinity Precipitation Assay DAPA
11:35

Screening for Functional Non-coding Genetic Variants Using Electrophoretic Mobility Shift Assay EMSA and DNA-affinity Precipitation Assay DAPA

Published on: August 21, 2016

13.0K

Related Concept Videos

Comparing Copy Number Variations and SNPs02:26

Comparing Copy Number Variations and SNPs

17.7K
Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
17.7K

Articles linked to this work by shared authors, journal, and citation graph.

Recovering the precolonial population structure of Khoe-San descendant populations.

Science advances·2026

Signatures of pathogen-driven selection and Austronesian gene flow of Papua New Guinea HLA alleles.

American journal of human genetics·2026

Recovering the pre-colonial population structure of Khoe-San descendant populations.

bioRxiv : the preprint server for biology·2025

Common DNA sequence variation influences epigenetic aging in African populations.

Communications biology·2025

The Indian Ocean slave trade and colonial expansion resulted in strong sex-biased admixture in South Africa.

American journal of human genetics·2025

No evidence for disassortative mating based on HLA in a small-scale, endogamous population.

bioRxiv : the preprint server for biology·2025

N4BP1 uses tandem KH domains to associate with EDC4 and mRNA decapping factors in P-bodies.

Communications biology·2026

The Soifua Manuia reference panel with 2,570 Samoan haplotypes improves genotype imputation quality among Samoans.

Communications biology·2026

YAP1 induces hepatocellular carcinoma via DNA demethylation rather than by canonical driver gene mutations.

Communications biology·2026

Non-coding regulatory variants in adolescent idiopathic scoliosis risk and pathogenesis.

Communications biology·2026

The TUBG meshwork is associated with centromere dynamics and micronuclear organization.

Communications biology·2026

Brain defence by the extracellular matrix protein Cochlin.

Communications biology·2026

Characterisation of the Novel HLA-DQB1*03:612 Allele by Sequencing-Based Typing.

HLA·2026

Identification of a New HLA-DRB5 Allele in a Chinese Han Individual, HLA-DRB5*01:01:17.

HLA·2026

The Novel HLA-DPB1*1903:01 Allele Was Likely Generated by a Recombination Event.

HLA·2026

Characterisation of the Novel HLA-C*16:01:53 Allele by Next-Generation Sequencing.

HLA·2026

Identification of the Novel HLA-F*01:37 Allele Using PolyseqOne Sequencing.

HLA·2026

The Novel HLA-DQB1*05:381 Allele Identified by Next-Generation Sequencing.

HLA·2026
See all related articles
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies
Jove
Visualize
Contact Us