Related Experiment Video

Updated: Oct 9, 2025

Personalized Peptide Arrays for Detection of HLA Alloantibodies in Organ Transplantation
08:07

Personalized Peptide Arrays for Detection of HLA Alloantibodies in Organ Transplantation

Published on: September 6, 2017

10.2K

Identification of the novel HLA-B*42:28 allele by next-generation sequencing

Jessica Ward1, Pamela Guthrie1, Leigh Keen1

  • 1Histocompatibility and Immunogenetics, NHSBT, Bristol, UK.

HLA
|December 21, 2021
PubMed

Abstract:

HLA-B*42:28 differs from HLA-B*42:01:01 by a single base substitution in exon 4 at codon 267.2.

Keywords:
haematopoietic stem cell transplantnational health service blood and transplantnext generation sequencing

More Related Videos

Author Spotlight: Advancing the Detection of Low-Frequency Mutations in Cancer Tissues
07:17

Author Spotlight: Advancing the Detection of Low-Frequency Mutations in Cancer Tissues

Published on: August 23, 2024

1.3K
T and B Cell Receptor Immune Repertoire Analysis using Next-generation Sequencing
08:59

T and B Cell Receptor Immune Repertoire Analysis using Next-generation Sequencing

Published on: January 12, 2021

8.4K

Related Experiment Videos

Last Updated: Oct 9, 2025

Personalized Peptide Arrays for Detection of HLA Alloantibodies in Organ Transplantation
08:07

Personalized Peptide Arrays for Detection of HLA Alloantibodies in Organ Transplantation

Published on: September 6, 2017

10.2K
Author Spotlight: Advancing the Detection of Low-Frequency Mutations in Cancer Tissues
07:17

Author Spotlight: Advancing the Detection of Low-Frequency Mutations in Cancer Tissues

Published on: August 23, 2024

1.3K
T and B Cell Receptor Immune Repertoire Analysis using Next-generation Sequencing
08:59

T and B Cell Receptor Immune Repertoire Analysis using Next-generation Sequencing

Published on: January 12, 2021

8.4K

Related Concept Videos

Next-generation Sequencing03:00

Next-generation Sequencing

93.8K
The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features....
93.8K
Genome-wide Association Studies-GWAS01:11

Genome-wide Association Studies-GWAS

14.7K
Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
14.7K

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

Effects of acoustic enrichment on settlement of a critically endangered broadcast spawning coral.

Scientific reports·2026

Preparation of Conspecific Alarm Cue From Fathead Minnows.

Journal of visualized experiments : JoVE·2026

Discovery of small molecule modulators of the thin filament that alter the contractile profile in a hypertrophic cardiomyopathy engineered tissue model.

The Journal of biological chemistry·2025

Evaluation of cross-generational exposure to microplastics and co-occurring contaminants on embryonic and larval behavior in fathead minnows, Pimephales promelas.

PeerJ·2025

An Open-Label, Single-Dose Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Safety, and Tolerability of Olpasiran in Chinese Participants With Elevated Serum Lipoprotein(a).

Clinical therapeutics·2025

Problem-Solving Skills Training for Parents of Children Undergoing Hematopoietic Stem Cell Transplantation: A Mixed Methods Feasibility Study.

Cancers·2025

Characterisation of the Novel HLA-DRB3*02:240 Allele by Sequencing-Based Typing.

HLA·2026

Characterisation of the Novel HLA-A*02:1205 and HLA-A*02:07:27 Alleles by Next-Generation Sequencing.

HLA·2026

The Novel HLA-A*02:1229 Allele Was Identified by Next-Generation Sequencing.

HLA·2026

A Novel Exonic Variant MICB*075 Was Identified in an Individual From Maharashtra, India.

HLA·2026

Characterisation of the Novel HLA-DQB1*02:80:02 Allele by Sequencing-Based Typing.

HLA·2026

Characterisation of the Novel HLA-A*32:207 Allele by Sequencing-Based Typing.

HLA·2026

Discovery of the Novel HLA-DQB1*05:386 Allele in a Brazilian Volunteer Donor.

HLA·2026

Identification of the Novel HLA-B*57:212 Allele by Next-Generation Sequencing.

HLA·2026

Characterisation of the Novel HLA-DRB3*01:127 Allele by Next-Generation Sequencing.

HLA·2026

Early-Onset TRNT1-Related SIFD Syndrome with an Additional Monoallelic C7 Variant: A Pediatric Case Report.

Diagnostics (Basel, Switzerland)·2026

Identification of the Novel HLA-DQB1*06:556 Allele 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