Evidence map›Paper›PMID 39013593›Full record

ArticleGenome research2024

High-fidelity, large-scale targeted profiling of microsatellites.

Caitlin A Loh, Danielle A Shields, Adam Schwing, Gilad D Evrony

Abstract read
In one paragraph

Article in Genome research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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

4 authors.

Caitlin A Loh *Center for Human Genetics and Genomics, New York University Grossman School of Medicine, New York, New York 10016, USA.
Danielle A Shields *Center for Human Genetics and Genomics, New York University Grossman School of Medicine, New York, New York 10016, USA.
Adam SchwingCenter for Human Genetics and Genomics, New York University Grossman School of Medicine, New York, New York 10016, USA.
Gilad D EvronyCenter for Human Genetics and Genomics, New York University Grossman School of Medicine, New York, New York 10016, USA; gilad.evrony@nyulangone.org.ORCID 0000-0001-7621-2630

Funding

Single-cell genomic approaches to study the cellular origins of brain tumorsDP5OD028158 · OD · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI EVRONY, GILAD DAVID · 2019 to 2023
$2.1M
NIH HHS DP5 OD028158
6 · The paper itself

Abstract

Microsatellites are highly mutable sequences that can serve as markers for relationships among individuals or cells within a population. The accuracy and resolution of reconstructing these relationships depends on the fidelity of microsatellite profiling and the number of microsatellites profiled. However, current methods for targeted profiling of microsatellites incur significant "stutter" artifacts that interfere with accurate genotyping, and sequencing costs preclude whole-genome microsatellite profiling of a large number of samples. We developed a novel method for accurate and cost-effective targeted profiling of a panel of more than 150,000 microsatellites per sample, along with a computational tool for designing large-scale microsatellite panels. Our method addresses the greatest challenge for microsatellite profiling-"stutter" artifacts-with a low-temperature hybridization capture that significantly reduces these artifacts. We also developed a computational tool for accurate genotyping of the resulting microsatellite sequencing data that uses an ensemble approach integrating three microsatellite genotyping tools, which we optimize by analysis of de novo microsatellite mutations in human trios. Altogether, our suite of experimental and computational tools enables high-fidelity, large-scale profiling of microsatellites, which may find utility in diverse applications such as lineage tracing, population genetics, ecology, and forensics.

Indexed as

Microsatellite RepeatsGenotypeGenotyping TechniquesHumansSequence Analysis, DNA

Identifiers

PMID39013593
PMCPMC11368184

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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.