Evidence map›Paper›PMID 36449158›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2023

Genotyping of Transposable Element Insertions Segregating in Human Populations Using Short-Read Realignments.

Xun Chen, Guillaume Bourque, Clément Goubert

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

3 authors at 2 institutions in 2 countries.

Xun ChenInstitute for the Advanced Study of Human Biology (ASHBi), Kyoto University, Kyoto, Japan. xunchen85@gmail.com.
Guillaume BourqueInstitute for the Advanced Study of Human Biology (ASHBi), Kyoto University, Kyoto, Japan.
Clément GoubertCanadian Centre for Computational Genomics, McGill University, Montreal, QC, Canada. goubert.clement@gmail.com.
Kyoto University · JPMcGill Genome Centre · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transposable element (TE) insertions are a major source of structural variation in the human genome. Due to the repetitive nature and biological importance of TEs, many bioinformatic tools have been developed to identify and genotype TE insertion polymorphisms using high-throughput short-reads. In this chapter, we outline recently developed methods to characterize TE insertion polymorphisms in human populations. We also provide detailed protocols to tackle this question primarily using three software: MELT2, ERVcaller, and TypeREF.

Indexed as

Computational BiologyDNA Transposable ElementsGenome, HumanGenotypeHumansPolymorphism, GeneticDNA Transposable ElementsHigh-throughput sequencingPolymorphismReference-based genotypingTransposable element

Identifiers

PMID36449158
OpenAlexW4310425710

What OpenQuestion holds

Textmetadata
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.