Evidence map›Paper›PMID 33476339›Full record

ArticlePLoS genetics2021

RAFFI: Accurate and fast familial relationship inference in large scale biobank studies using RaPID.

Ardalan Naseri, Junjie Shi, Xihong Lin, Shaojie Zhang, Degui Zhi

Abstract read
In one paragraph

Article in PLoS genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Secure Discovery of Genetic Relatives across Large-Scale and Distributed Genomic Datasets.Research in computational molecular biology : ... Annual International Conference, RECOMB ... : proceedings. RECOMB (Conference : 2005- )
    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.

Ardalan NaseriSchool of Biomedical Informatics, The University of Texas Health Science Center at Houston, Houston, Texas, United States of America.ORCID 0000-0002-2747-2193
Junjie ShiDepartment of Computer Science, Rice University, Houston, Texas, United States of America.ORCID 0000-0001-5073-9653
Xihong LinDepartment of Biostatistics, Harvard T. H. Chan School of Public Health, Boston, Massachusetts, United States of America.ORCID 0000-0001-7067-7752
Shaojie ZhangDepartment of Computer Science, University of Central Florida, Orlando, Florida, United States of America.ORCID 0000-0002-4051-5549
Degui ZhiSchool of Biomedical Informatics, The University of Texas Health Science Center at Houston, Houston, Texas, United States of America.

Funding

The Baylor-Hopkins Clinical Genomics Center for All of UsOT2OD002751 · OD · BAYLOR COLLEGE OF MEDICINE · PI BOERWINKLE, ERIC A., DOHENY, KIMBERLY F · 2018 to 2023
$152.8M
Translating Molecular and Clinical Data to Population Lung Cancer Risk AssessmentU19CA203654 · NCI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Christopher I. Amos · 2017 to 2026
$23.7M
Statistical Methods for Analysis of Massive Genetic and Genomic Data in Cancer ResearchR35CA197449 · NCI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI XIHONG LIN · 2015 to 2026
$10.9M
Powering whole genome sequence-based genetic discovery for common human diseases- Extended 2021-2022.U01HG009088 · NHGRI · HARVARD SCHOOL OF PUBLIC HEALTH · PI LIN, XIHONG, NEALE, BENJAMIN MICHAEL · 2016 to 2021
$5.1M
Scalable methods for identity by descentR01HG010086 · NHGRI · YALE UNIVERSITY · PI Shaojie Zhang, Degui Zhi · 2018 to 2026
$4.9M
Medical Research Council MC_PC_17228Medical Research Council MC_QA137853NCI NIH HHS R35 CA197449NCI NIH HHS U19 CA203654NHGRI NIH HHS R01 HG010086NHGRI NIH HHS U01 HG009088NIH HHS OT2 OD002751
6 · The paper itself

Abstract

Inference of relationships from whole-genome genetic data of a cohort is a crucial prerequisite for genome-wide association studies. Typically, relationships are inferred by computing the kinship coefficients (ϕ) and the genome-wide probability of zero IBD sharing (π0) among all pairs of individuals. Current leading methods are based on pairwise comparisons, which may not scale up to very large cohorts (e.g., sample size >1 million). Here, we propose an efficient relationship inference method, RAFFI. RAFFI leverages the efficient RaPID method to call IBD segments first, then estimate the ϕ and π0 from detected IBD segments. This inference is achieved by a data-driven approach that adjusts the estimation based on phasing quality and genotyping quality. Using simulations, we showed that RAFFI is robust against phasing/genotyping errors, admix events, and varying marker densities, and achieves higher accuracy compared to KING, the current leading method, especially for more distant relatives. When applied to the phased UK Biobank data with ~500K individuals, RAFFI is approximately 18 times faster than KING. We expect RAFFI will offer fast and accurate relatedness inference for even larger cohorts.

Indexed as

Models, GeneticBiological Specimen BanksGenome, HumanGenome-Wide Association StudyGenotyping TechniquesHaplotypesHumansPedigreePolymorphism, Single Nucleotide

Identifiers

PMID33476339
PMCPMC7853505

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.