Evidence map›Paper›PMID 34251753›Full record

ArticleInternational journal of laboratory hematology2021

Breakpoint characterization of a rare alpha

Quint P Hottentot, Emile de Meijer, Henk P J Buermans, Stefan J White, Cornelis L Harteveld

Open access · hybridAbstract read
In one paragraph

Article in International journal of laboratory hematology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 44% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Characterization of New Alpha Zero (αDiagnostics (Basel, Switzerland) · 2023
    Article
  2. Detection of hemoglobin H disease by long molecule sequencing.Journal of clinical laboratory analysis · 2022
    Article
  3. Breakpoint characterization of a rare alphaInternational journal of laboratory hematology · 2021
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Quint P HottentotDepartment of Clinical Genetics, Leiden University Medical Centre, Leiden, the Netherlands.ORCID https://orcid.org/0000-0003-2811-4715
Emile de MeijerLeiden Genome Technology Centre, Leiden University Medical Centre, Leiden, the Netherlands.
Henk P J BuermansLeiden Genome Technology Centre, Leiden University Medical Centre, Leiden, the Netherlands.
Stefan J WhiteLeiden Genome Technology Centre, Leiden University Medical Centre, Leiden, the Netherlands.
Cornelis L HarteveldDepartment of Clinical Genetics, Leiden University Medical Centre, Leiden, the Netherlands.
Leiden University Medical Center · NLLeiden University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe high-sequence homology of the α-globin-gene cluster is responsible for microhomology-mediated recombination events during meiosis, resulting in a high density of deletion breakpoints within a 10 kb region. Commonly used deletion detection methods, such as multiplex ligation-dependent probe amplification (MLPA) and Southern blot, cannot exactly define the breakpoints. This typically requires long-range PCR, which is not always successful. Targeted locus amplification (TLA) is a targeted enrichment method that can be used to sequence up to 70 kb of neighboring DNA sequences without prior knowledge about the target site.

methodsGenomic DNA (gDNA) TLA is a technique that folds isolated DNA, ensuring that adjacent loci are in a close spatial proximity. Subsequent digestion and religation form DNA circles that are amplified using fragment-specific inverse primers, creating a library that is suitable for Illumina sequencing.

resultsHere, we describe the characterization of a rare 16 771 bp deletion, utilizing gDNA TLA with a single inverse PCR primer set on one end of the breakpoint. Primers for breakpoint PCR were designed to confirm the deletion breakpoints and were consequently used to characterize the same deletion in 10 additional carriers sharing comparable hematologic data and similar MLPA results.

conclusionsThe gDNA TLA technology was successfully used to identify deletion breakpoints within the alpha-globin cluster. The deletion was described only once in an earlier study as the --

Indexed as

AllelesChromosome BreakpointsSequence Deletionalpha-Globinsalpha-ThalassemiaGenetic TestingGenomic LibraryHigh-Throughput Nucleotide SequencingHumansNucleic Acid Amplification TechniquesPolymerase Chain Reactionalpha-Globinsclinical geneticshemoglobinopathymolecular diagnosticstargeted sequencingthalassemiaTLA

Identifiers

PMID34251753
PMCPMC9291876
OpenAlexW3178698029

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.