SDFA: a standardized decomposition format and toolkit for efficient analysis of structural variants in large-scale population genomic studies

Structural variants (SVs) contribute significantly to genetic diversity yet present computational challenges during analysis. We introduce SDFA, a standardized decomposition format and toolkit for efficient analysis of SVs in large-scale population genomics. SDFA efficiently stores and retrieves all SV types while providing algorithms for consistent SV merging, memory-efficient annotation, and precise gene feature annotation across large cohorts. SDFA outperforms existing tools, achieving at least 17.64 times faster merging than four tools and 120.93 times faster annotation than three tools, and uniquely handles complex SVs. We validate SDFA on 895,054 SVs from 150,119 individuals in the UK Biobank dataset.

Authors

Institutions

Publication Details

Journal
Genome biology
Published
2025-09-30
DOI
https://doi.org/10.1186/s13059-025-03730-3
Primary Topic
Genomics and Rare Diseases
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

SDFA: a standardized decomposition format and toolkit for efficient analysis of structural variants in large-scale population genomic studies

Nan Lin, Yangyang Yuan, Bin Tang, Miaoxin Li et al.
Genome biology
Genomics and Rare Diseases
article

SDFA: a standardized decomposition format and toolkit for efficient analysis of structural variants in large-scale population genomic studies

Nan Lin, Yangyang Yuan, Bin Tang, Miaoxin Li, Rui Tan, Junhao Liang, Wenjie Peng, Lihang Ye, Liubin Zhang, Yifei Wang, Zhi Liu, Fang Li, Chao Xue, Hui Jiang
article en

Abstract

Structural variants (SVs) contribute significantly to genetic diversity yet present computational challenges during analysis. We introduce SDFA, a standardized decomposition format and toolkit for efficient analysis of SVs in large-scale population genomics. SDFA efficiently stores and retrieves all SV types while providing algorithms for consistent SV merging, memory-efficient annotation, and precise gene feature annotation across large cohorts. SDFA outperforms existing tools, achieving at least 17.64 times faster merging than four tools and 120.93 times faster annotation than three tools, and uniquely handles complex SVs. We validate SDFA on 895,054 SVs from 150,119 individuals in the UK Biobank dataset.

Genome biologyVol. 26(1)
Zhejiang Chinese Medical University (CN), Ministry of Education of the People's Republic of China (CN), Sun Yat-sen University (CN), Third Affiliated Hospital of Zhengzhou University (CN)
National Natural Science Foundation of China, Basic and Applied Basic Research Foundation of Guangdong Province
Openalex Percentile: Top 71%
Genomics and Rare Diseases
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.