Evidence map›Paper›PMID 37166451›Full record

ArticleBioinformatics (Oxford, England)2023

RaPID-Query for fast identity by descent search and genealogical analysis.

Yuan Wei, Ardalan Naseri, Degui Zhi, Shaojie Zhang

Open access · goldAbstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 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
1.3field-weighted citation impact, top 18% 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, 4 citations in OpenAlex.

  1. Article
  2. An Efficient Dynamic Data Structure for Haplotype Matching and Compression on Biobank-Scale Data.Journal of computational biology : a journal of computational molecular cell biology · 2026
    Article
  3. DynamicbioRxiv : the preprint server for biology · 2025
    Article
  4. Haplotype Matching with GBWT for Pangenome Graphs.bioRxiv : the preprint server for biology · 2025
    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 at 2 institutions in 1 country.

Yuan WeiDepartment of Computer Science, University of Central Florida, Orlando, FL 32816, United States.
Ardalan NaseriSchool of Biomedical Informatics, University of Texas Health Science Center at Houston, Houston, TX 77030, United States.
Degui ZhiSchool of Biomedical Informatics, University of Texas Health Science Center at Houston, Houston, TX 77030, United States.
Shaojie ZhangDepartment of Computer Science, University of Central Florida, Orlando, FL 32816, United States.ORCID 0000-0002-4051-5549
The University of Texas Health Science Center at Houston · USUniversity of Central Florida · US

Funding

Scalable methods for identity by descentR01HG010086 · NHGRI · YALE UNIVERSITY · PI Shaojie Zhang, Degui Zhi · 2018 to 2026
$4.9M
Genome Informatics For Biobank-scale DataR56HG011509 · NHGRI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI ZHANG, SHAOJIE, ZHI, DEGUI · 2021 to 2021
$616k
NHGRI NIH HHS R01 HG010086NHGRI NIH HHS R56 HG011509
6 · The paper itself

Abstract

motivationDue to the rapid growth of the genetic database size, genealogical search, a process of inferring familial relatedness by identifying DNA matches, has become a viable approach to help individuals finding missing family members or law enforcement agencies locating suspects. A fast and accurate method is needed to search an out-of-database individual against millions of individuals. Most existing approaches only offer all-versus-all within panel match. Some prototype algorithms offer one-versus-all query from out-of-panel individual, but they do not tolerate errors.

resultsA new method, random projection-based identity-by-descent (IBD) detection (RaPID) query, is introduced to make fast genealogical search possible. RaPID-Query identifies IBD segments between a query haplotype and a panel of haplotypes. By integrating matches over multiple PBWT indexes, RaPID-Query manages to locate IBD segments quickly with a given cutoff length while allowing mismatched sites. A single query against all UK biobank autosomal chromosomes was completed within 2.76 seconds on average, with the minimum length 7 cM and 700 markers. RaPID-Query achieved a 0.016 false negative rate and a 0.012 false positive rate simultaneously on a chromosome 20 sequencing panel having 86 265 sites. This is comparable to the state-of-the-art IBD detection method TPBWT(out-of-sample) and Hap-IBD. The high-quality IBD segments yielded by RaPID-Query were able to distinguish up to fourth degree of the familial relatedness for a given individual pair, and the area under the receiver operating characteristic curve values are at least 97.28%. AVAILABILITY AND IMPLEMENTATION: The RaPID-Query program is available at https://github.com/ucfcbb/RaPID-Query.

Indexed as

AlgorithmsChromosomesHaplotypesHumansSequence Analysis

Identifiers

PMID37166451
PMCPMC10244210
OpenAlexW4376131741

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.