Weiming He

Weiming He

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Weiming He

BGI Research , Shenzhen 518083

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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15 October 2018 in Bioinformatics
Verified
Journal Article
Closed access
PDF file
CZChi Zhang
Chi Zhang
SDShan-Shan Dong
Shan-Shan Dong
JXJun-Yang Xu
Jun-Yang Xu
WHWei-Ming He
Wei-Ming He
TYTielin Yang
Tielin Yang
Motivation: Linkage disequilibrium (LD) decay is of great interest in population genetic studies. However, no tool is available now to do LD decay analysis from variant call format (VCF) files directly. In addition, generation of pair-wise LD measurements for whole genome SNPs usually resulting in large storage wasting files. Results: We developed PopLDdecay, an open source software, for LD decay analysis from VCF files. It is fast and is able to handle large number of variants from sequencing data. It is also storage saving by avoiding exporting pair-wise results of LD measurements. Subgroup analyses are also supported. Availability and implementation: PopLDdecay is freely available at https://github.com/BGI-shenzhen/PopLDdecay.

30 October 2020 in Briefings in Bioinformatics
Verified
Journal Article
Closed access
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SDShan-Shan Dong
Shan-Shan Dong
WHWei-Ming He
Wei-Ming He
JJJing-Jing Ji
Jing-Jing Ji
CZChi Zhang
Chi Zhang
YGYan Guo
Yan Guo
TYTielin Yang
Tielin Yang
The triangular correlation heatmap aiming to visualize the linkage disequilibrium (LD) pattern and haplotype block structure of SNPs is ubiquitous component of population-based genetic studies. However, current tools suffered from the problem of time and memory consuming. Here, we developed LDBlockShow, an open source software, for visualizing LD and haplotype blocks from variant call format files. It is time and memory saving. In a test dataset with 100 SNPs from 60 000 subjects, it was at least 10.60 times faster and used only 0.03–13.33% of physical memory as compared with other tools. In addition, it could generate figures that simultaneously display additional statistical context (e.g. association P-values) and genomic region annotations. It can also compress the SVG files with a large number of SNPs and support subgroup analysis. This fast and convenient tool will facilitate the visualization of LD and haplotype blocks for geneticists.

29 April 2019 in Nature Genetics
Verified
Journal Article
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Rajeev VarshneyRajeev Varshney
Rajeev Varshney
Mahendar ThudiMahendar Thudi
Mahendar Thudi
Manish RoorkiwalManish Roorkiwal
Manish Roorkiwal
WHWeiming He
Weiming He
HUHari D. Upadhyaya
Hari D. Upadhyaya
XLXin Liu
Xin Liu

1 March 2023 in Bioinformatics
Verified
Journal Article
Open access
PDF file
WHWeiming He
Weiming He
JYJian Yang
Jian Yang
YJYi Jing
Yi Jing
LXLian Xu
Lian Xu
KYKang Yu
Kang Yu
XFXiaodong FANG
Xiaodong FANG
Large-scale comparative genomic studies have provided important insights into species evolution and diversity, but also lead to a great challenge to visualize. Quick catching or presenting key information hidden in the vast amount of genomic data and relationships among multiple genomes requires an efficient visualization tool. However, current tools for such visualization remain inflexible in layout and/or require advanced computation skills, especially for visualization of genome-based synteny. Here, we developed an easy-to-use and flexible layout tool, NGenomeSyn (multiple (N) Genome Synteny), for publication-ready visualization of syntenic relationships of the whole genome or local region and genomic features (e.g. repeats, structural variations, genes) across multiple genomes with a high customization. NGenomeSyn provides an easy way for its users to visualize a large amount of data with a rich layout by simply adjusting options for moving, scaling, and rotation of target genomes. Moreover, NGenomeSyn could be applied on the visualization of relationships on non-genomic data with similar input formats. NGenomeSyn is freely available at GitHub (https://github.com/hewm2008/NGenomeSyn) and Zenodo (https://doi.org/10.5281/zenodo.7645148). Supplementary data are available at Bioinformatics online.

24 September 2022 in Nature Communications
Verified
Journal Article
Open access
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XTXiaoling Tong
Xiaoling Tong
MHMin-Jin Han
Min-Jin Han
KLKunpeng Lu
Kunpeng Lu
STShuaishuai Tai
Shuaishuai Tai
SLShubo Liang
Shubo Liang
FDFangyin Dai
Fangyin Dai
The silkwormBombyx moriis an important economic insect for producing silk, the “queen of fabrics”. The currently available genomes limit the understanding of its genetic diversity and the discovery of valuable alleles for breeding. Here, we deeply re-sequence 1,078 silkworms and assemble long-read genomes for 545 representatives. We construct a high-resolution pan-genome dataset representing almost the entire genomic content in the silkworm. We find that the silkworm population harbors a high density of genomic variants and identify 7308 new genes, 4260 (22%) core genes, and 3,432,266 non-redundant structure variations (SVs). We reveal hundreds of genes and SVs that may contribute to the artificial selection (domestication and breeding) of silkworm. Further, we focus on four genes responsible, respectively, for two economic (silk yield and silk fineness) and two ecologically adaptive traits (egg diapause and aposematic coloration). Taken together, our population-scale genomic resources will promote functional genomics studies and breeding improvement for silkworm.

12 December 2014 in GigaScience
Verified
Journal Article
Open access
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CLCai Li
Cai Li
YZYong Zhang
Yong Zhang
JLJianwen Li
Jianwen Li
LKLesheng Kong
Lesheng Kong
HHHaofu Hu
Haofu Hu
GZGuojie Zhang
Guojie Zhang
Background. Penguins are flightless aquatic birds widely distributed in the Southern Hemisphere. The distinctive morphological and physiological feature