arrow
Z

Zilin Li

Northeast Normal University
H指数:21
被引数:3,265

个人简介

暂无内容

教育背景

暂无内容

工作经历

暂无内容

荣誉奖项

暂无内容

Comparison of variant callers using 60 532 multi-ancestry whole genome sequences

比较不同变异调用器在60532例多祖先全基因组序列中的应用

2026-03-010
PRE
cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regions

cellSTAAR:整合基于单细胞测序的功能数据,以提升非编码区域稀有变异关联检验的功效

2025-12-310
PRE
FAVOR 2.0: A reengineered functional annotation of variants online resource for interpreting genomic variation

FAVOR 2.0:一个用于解释基因组变异的在线资源,该资源对变异的功能注释进行了再工程化

2025-12-011
PRE
Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height

333,100个体的全基因组测序揭示了罕见的非编码单一变异和与身高的聚集关联

2024-10-032
OAAI
Whole genome sequencing based analysis of inflammation biomarkers in the Trans-Omics for Precision Medicine (TOPMed) consortium
2024-05-011
PRE
Whole-Genome Sequencing Analysis of Human Metabolome in Multi-Ethnic Populations (vol 14, 3111, 2023)
2023-10-190
OAAI
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study
2023-10-012
OAAI
Whole-Genome Sequencing Analysis of Human Metabolome in Multi-Ethnic Populations

多民族人群人类代谢组的全基因组测序分析

2023-05-308
OAAI
Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies

大型全基因组测序研究中罕见变异关联的强大、可扩展和资源高效的荟萃分析

2022-12-2320
OA
FAVOR: functional annotation of variants online resource and annotator for variation across the human genome

青睐: 变体的功能注释在线资源和人类基因组变异的注释器

2022-11-0941
OAAI
A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies

检测大规模全基因组测序研究的非编码罕见变异关联的框架

2022-10-2739
OA
Whole genome sequence analysis of blood lipid levels in >66,000 individuals

> 66,000个人血脂水平的全基因组序列分析

2022-10-1124
OAAI