Evidence map›Paper›PMID 41446504›Full record

ArticleNAR genomics and bioinformatics2025

Pastrami: a fast and efficient algorithm for fine-scale genetic ancestry inference.

Andrew B Conley, Lavanya Rishishwar, Shivam Sharma, Emily T Norris, I King Jordan, Leonardo Mariño-Ramírez

Abstract read
In one paragraph

Article in NAR genomics and bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Andrew B ConleyNational Institute of Minority Health and Health Disparities, National Institutes of Health, Bethesda, MD 20892, United States.
Lavanya RishishwarNational Institute of Minority Health and Health Disparities, National Institutes of Health, Bethesda, MD 20892, United States.
Shivam SharmaSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA 30332, United States.ORCID https://orcid.org/0000-0003-3577-1596
Emily T NorrisNational Institute of Minority Health and Health Disparities, National Institutes of Health, Bethesda, MD 20892, United States.
I King JordanASRT,Inc., Smyrna, GA 30080, United States.ORCID https://orcid.org/0000-0003-4996-2203
Leonardo Mariño-RamírezNational Institute of Minority Health and Health Disparities, National Institutes of Health, Bethesda, MD 20892, United States.ORCID https://orcid.org/0000-0002-5716-8512

Funding

Genomics and Biobank Research for Health EquityZIAMD000018 · NIMHD · NATIONAL INSTITUTE ON MINORITY HEALTH AND HEALTH DISPARITIES · PI MARIÑO-RAMÍREZ, LEONARDO · 2020 to 2025
$2.7M
Epidemiology and Genomics of Health DisparitiesZIAMD000016 · NIMHD · NATIONAL INSTITUTE ON MINORITY HEALTH AND HEALTH DISPARITIES · PI MARINO-RAMIREZ, LEONARDO · 2019 to 2021
$1.6M
Intramural NIH HHS ZIA MD000016Intramural NIH HHS ZIA MD000018
6 · The paper itself

Abstract

Genomics research increasingly relies on large population biobanks that include many thousands of participants. However, current genetic ancestry inference methods are computationally inefficient and prohibitively slow when applied to such large cohorts. The aim of this work was to develop a fast and efficient algorithm for fine-scale genetic ancestry inference on biobank-size cohorts. The Pastrami algorithm that we developed performs supervised genetic ancestry inference by comparing haplotypes between query and global reference samples, creating query and reference haplotype copying vectors, and relating them via non-negative least squares regression to estimate ancestry fractions. We used Pastrami for ancestry inference on genomic data sets from Africa, the Americas, and the United Kingdom, comparing its accuracy and runtime performance to the most widely used haplotype-based ancestry inference methods. Pastrami ancestry estimates are highly similar to estimates from the ChromoPainter and RFMix programs. The total CPU time required by Pastrami increases linearly with the number of samples, and it achieves ∼45× faster runtime than ChromoPainter. When run on 488 377 UK Biobank and 3433 reference samples, Pastrami used 2340 CPU hours compared to ∼105 000 CPU hours for ChromoPainter. The Pastrami program and documentation are made freely available on GitHub: https://github.com/healthdisparities/pastrami.

Indexed as

AlgorithmsGenetics, PopulationGenomicsSoftwareHaplotypesHumans

Identifiers

PMID41446504
PMCPMC12723237

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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.