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

Conley Andrew B, AB Rishishwar, Lavanya L et al.

41446504 PubMed ID
9 Authors
2025-12-23 Published
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

CA
Conley Andrew B
AR
AB Rishishwar
LL
Lavanya L
SS
Sharma Shivam
SN
S Norris
ET
Emily T ET
JI
Jordan I King
IM
IK Mariño-Ramírez
LL
Leonardo L
Chapter II

Abstract

Summary of the research findings

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.

Chapter III

AI-Generated Summary

AI-generated by DNAGENICS

Independent AI summary of ancestry and genetic findings from the published study

Important: This summary is AI-generated by DNAGENICS for informational purposes only. It was not created by, affiliated with, or endorsed by the researchers behind the original publication, and is based solely on that published research. It may contain errors or omissions. DNAGENICS disclaims all liability for any inaccuracies or consequences arising from use of this information. Verify all information against the original publication. This is not professional scientific review or medical advice.

Summary

Key Findings

Ancestry Insights

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Historical Context