Evidence map›Paper›PMID 36701310›Full record

ArticlePloS one2023

The Genomic landscape of short tandem repeats across multiple ancestries.

Prashanth Vijayaraghavan, Sergey Batalov, Yan Ding, Erica Sanford, Stephen F Kingsmore, David Dimmock, Charlotte Hobbs, Matthew Bainbridge

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 28% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. 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

8 authors at 2 institutions in 1 country.

Prashanth VijayaraghavanRady Children's Institute for Genomic Medicine, San Diego, CA, United States of America.ORCID 0000-0001-7661-236X
Sergey BatalovRady Children's Institute for Genomic Medicine, San Diego, CA, United States of America.
Yan DingRady Children's Institute for Genomic Medicine, San Diego, CA, United States of America.
Erica SanfordRady Children's Institute for Genomic Medicine, San Diego, CA, United States of America.
Stephen F KingsmoreRady Children's Institute for Genomic Medicine, San Diego, CA, United States of America.
David DimmockRady Children's Institute for Genomic Medicine, San Diego, CA, United States of America.
Charlotte HobbsRady Children's Institute for Genomic Medicine, San Diego, CA, United States of America.
Matthew BainbridgeRady Children's Institute for Genomic Medicine, San Diego, CA, United States of America.
Children’s Institute · USCedars-Sinai Medical Center · US

Funding

Oligogenic Models of CardiomyopathyR01HL145175 · NHLBI · RADY PEDIATRIC GENOMICS & SYSTEMS MEDICINE INSTITUTE · PI BAINBRIDGE, MATTHEW NEIL · 2019 to 2022
$3.0M
NHLBI NIH HHS R01 HL145175
6 · The paper itself

Abstract

Short Tandem Repeats (STRs) have been found to play a role in a myriad of complex traits and genetic diseases. We examined the variability in the lengths of over 850,000 STR loci in 996 children with suspected genetic disorders and 1,178 parents across six separate ancestral groups: Africans, Europeans, East Asians, Admixed Americans, Non-admixed Americans, and Pacific Islanders. For each STR locus we compared allele length between and within each ancestry group. In relation to Europeans, admixed Americans had the most similar STR lengths with only 623 positions either significantly expanded or contracted, while the divergence was highest in Africans, with 4,933 chromosomal positions contracted or expanded. We also examined probands to identify STR expansions at known pathogenic loci. The genes TCF4, AR, and DMPK showed significant expansions with lengths 250% greater than their various average allele lengths in 49, 162, and 11 individuals respectively. All 49 individuals containing an expansion in TCF4 and six individuals containing an expansion in DMPK presented with allele lengths longer than the known pathogenic length for these genes. Next, we identified individuals with significant expansions in highly conserved loci across all ancestries. Eighty loci in conserved regions met criteria for divergence. Two of these individuals were found to have exonic STR expansions: one in ZBTB4 and the other in SLC9A7, which is associated with X-linked mental retardation. Finally, we used parent-child trios to detect and analyze de novo mutations. In total, we observed 3,219 de novo expansions, where proband allele lengths are greater than twice the longest parental allele length. This work helps lay the foundation for understanding STR lengths genome-wide across ancestries and may help identify new disease genes and novel mechanisms of pathogenicity in known disease genes.

Indexed as

GenomicsMicrosatellite RepeatsAllelesExonsHigh-Throughput Nucleotide SequencingHumans

Identifiers

PMID36701310
PMCPMC9879404
OpenAlexW4318142975

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.