Mingyao Li
Molecular Biology · Nature Methods · 2007–2021
A researcher in the Science corpus: 12 papers; trusts 12 researchers and is trusted by 9 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 125 citations into it; #3,764 of 17,773 by trust here, #1,821 by citations
- Genetics — 93 citations into it; #1,187 of 6,854 by trust here, #226 by citations
- Immunology — 17 citations into it
Whom Mingyao Li trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- C. Dong
- Johan T. den Dunnen
- Phil Hyoun Lee
- Frank Steemers
- Kim D. Pruitt
- V. Ramensky
- Kevin L. Gunderson
- Katherine S. Pollard
- Tong Tong Wu
- Adam C. Siepel
Who trusts Mingyao Li overall
- Xiaoming Liu
- Xueqiu Jian
- Hui Yang
- Eric Boerwinkle
- Kai Wang
- Xiao-Xia Chang
- Karen Eilbeck
- A. Young
- Umadevi Paila
- Xiaoming Liu
Papers from Mingyao Li's perspective
Ordered by how strongly the researchers Mingyao Li trusts endorse each paper. Same corpus, a different order for every researcher.
- Detection of large-scale variation in the human genome (Nature Genetics)
- BLAT--the BLAST-like alignment tool. (Genome Research)
- [Structural variation in the human genome]. (Yi chuan = Hereditas)
- Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry (Nature)
- Fine-scale structural variation of the human genome (Nature Genetics)
- NCBI Reference Sequence (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins (Nucleic Acids Res.)
- Segmental duplications: organization and impact within the current human genome project assembly. (Genome Research)
- Human non-synonymous SNPs: server and survey. (Nucleic Acids Research)
- Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes.
- Regularization Paths for Generalized Linear Models via Coordinate Descent
Their papers
- ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data (2010) — 13,554 citations
- SAVER: Gene expression recovery for single-cell RNA sequencing (2018) — 673 citations
- Genome-wide association of early-onset myocardial infarction with common single nucleotide polymorphisms, common copy number variants, and rare copy number variants (2009) — 1,094 citations
- SpaGCN: Integrating gene expression, spatial location and histology to identify spatial domains and spatially variable genes by graph convolutional network (2021) — 962 citations
- Single-cell transcriptomics of the mouse kidney reveals potential cellular targets of kidney disease (2018) — 955 citations
- Analysing biological pathways in genome-wide association studies (2010) — 815 citations
- PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. (2007) — 1,861 citations
- Deep learning enables accurate clustering with batch effect removal in single-cell RNA-seq analysis (2020) — 372 citations
- Bulk tissue cell type deconvolution with multi-subject single-cell expression reference (2018) — 796 citations
- Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies (2011) — 531 citations
- Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study (2012) — 2,232 citations
- Biological, Clinical, and Population Relevance of 95 Loci for Blood Lipids (2010) — 3,781 citations