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From genome-wide associations to candidate causal variants by statistical fine-mapping

Nature reviews. Genetics, 2018-08, Vol.19 (8), p.491-504

2018

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UMI-count modeling and differential expression analysis for single-cell RNA sequencing

Genome Biology, 2018-05, Vol.19 (1), p.70-70, Article 70

2018

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A Review of Single-Cell RNA-Seq Annotation, Integration, and Cell-Cell Communication

Cells (Basel, Switzerland), 2023-07, Vol.12 (15), p.1970

2023

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China's Grand Strategy: A Framework Analysis

1st Edition 2020, 2020

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Genetic Risk for Subsequent Neoplasms Among Long-Term Survivors of Childhood Cancer

Journal of clinical oncology, 2018-07, Vol.36 (20), p.2078-2087

2018

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A rare variant analysis framework using public genotype summary counts to prioritize disease-predisposition genes

Nature communications, 2022-05, Vol.13 (1), p.2592-2592, Article 2592

2022

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Incorporating Functional Annotations for Fine-Mapping Causal Variants in a Bayesian Framework Using Summary Statistics

Genetics (Austin), 2016-11, Vol.204 (3), p.933-958

2016

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Recent advances and challenges of rare variant association analysis in the biobank sequencing era

Frontiers in genetics, 2022-10, Vol.13, p.1014947-1014947

2022

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Genome-wide mapping of cancer dependency genes and genetic modifiers of chemotherapy in high-risk hepatoblastoma

Nature communications, 2023-07, Vol.14 (1), p.4003-27, Article 4003

2023

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Polygenic risk scores for major depressive disorder and neuroticism as predictors of antidepressant response: Meta-analysis of three treatment cohorts

PloS one, 2018-09, Vol.13 (9), p.e0203896

2018

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Study on dynamic and static elastic moduli of shale oil by different loading methods

Unconventional Resources, 2023, Vol.3, p.183-191

2023

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Chinese Diplomacy in the New Era

1st Edition 2021, 2021

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A comparison of methods accounting for batch effects in differential expression analysis of UMI count based single cell RNA sequencing

Computational and structural biotechnology journal, 2020-01, Vol.18, p.861-873

2020

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Germline landscape of RPA1, RPA2 and RPA3 variants in pediatric malignancies: identification of RPA1 as a novel cancer predisposition candidate gene

Frontiers in oncology, 2023-10, Vol.13, p.1229507-1229507

2023

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Protocol for immunophenotyping out-of-hospital cardiac arrest patients

STAR protocols, 2024-03, Vol.5 (1), p.102874-102874, Article 102874

2024

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Machine learning suggests polygenic risk for cognitive dysfunction in amyotrophic lateral sclerosis

EMBO molecular medicine, 2021-01, Vol.13 (1), p.e12595-n/a

2021

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XAF1 as a modifier of p53 function and cancer susceptibility

Science advances, 2020-06, Vol.6 (26), p.eaba3231-eaba3231

2020

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Identification of TCF3 germline variants in pediatric B-cell acute lymphoblastic leukemia

Blood advances, 2023-05, Vol.7 (10), p.2177-2180

2023

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S107: IDENTIFICATION AND CHARACTERIZATION OF GERMLINE NBN VARIANTS RELATED TO B‐ALL PREDISPOSITION

HemaSphere, 2023-08, Vol.7 (S3), p.e4470514-n/a

2023

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Automated ventricular systems segmentation in brain CT images by combining low-level segmentation and high-level template matching

BMC medical informatics and decision making, 2009-11, Vol.9 Suppl 1 (Suppl 1), p.S4-S4, Article S4

2009

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MethylPCA: a toolkit to control for confounders in methylome-wide association studies

BMC bioinformatics, 2013-03, Vol.14 (1), p.74-74, Article 74

2013

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Accurate genomic variant detection in single cells with primary template-directed amplification

Proceedings of the National Academy of Sciences - PNAS, 2021-06, Vol.118 (24), p.1

2021

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Metabolic heterogeneity underlies reciprocal fates of TH17 cell stemness and plasticity

Nature (London), 2018-12, Vol.565 (7737), p.101-105

2018

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A piezoelectric energy harvester based on internal resonance

Acta mechanica Sinica, 2015-05, Vol.31 (2), p.223-228

2015

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Fine Mapping Causal Variants with an Approximate Bayesian Method Using Marginal Test Statistics

Genetics (Austin), 2015-07, Vol.200 (3), p.719-736

2015

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From genome-wide associations to candidate causal variants by statistical fine-mapping

UMI-count modeling and differential expression analysis for single-cell RNA sequencing

A Review of Single-Cell RNA-Seq Annotation, Integration, and Cell-Cell Communication

China's Grand Strategy: A Framework Analysis

Genetic Risk for Subsequent Neoplasms Among Long-Term Survivors of Childhood Cancer

A rare variant analysis framework using public genotype summary counts to prioritize disease-predisposition genes

Incorporating Functional Annotations for Fine-Mapping Causal Variants in a Bayesian Framework Using Summary Statistics

Recent advances and challenges of rare variant association analysis in the biobank sequencing era

Genome-wide mapping of cancer dependency genes and genetic modifiers of chemotherapy in high-risk hepatoblastoma

Polygenic risk scores for major depressive disorder and neuroticism as predictors of antidepressant response: Meta-analysis of three treatment cohorts

Study on dynamic and static elastic moduli of shale oil by different loading methods

Chinese Diplomacy in the New Era

A comparison of methods accounting for batch effects in differential expression analysis of UMI count based single cell RNA sequencing

Germline landscape of RPA1, RPA2 and RPA3 variants in pediatric malignancies: identification of RPA1 as a novel cancer predisposition candidate gene

Protocol for immunophenotyping out-of-hospital cardiac arrest patients

Machine learning suggests polygenic risk for cognitive dysfunction in amyotrophic lateral sclerosis

XAF1 as a modifier of p53 function and cancer susceptibility

Identification of TCF3 germline variants in pediatric B-cell acute lymphoblastic leukemia

S107: IDENTIFICATION AND CHARACTERIZATION OF GERMLINE NBN VARIANTS RELATED TO B‐ALL PREDISPOSITION

Automated ventricular systems segmentation in brain CT images by combining low-level segmentation and high-level template matching

MethylPCA: a toolkit to control for confounders in methylome-wide association studies

Accurate genomic variant detection in single cells with primary template-directed amplification

Metabolic heterogeneity underlies reciprocal fates of TH17 cell stemness and plasticity

A piezoelectric energy harvester based on internal resonance

Fine Mapping Causal Variants with an Approximate Bayesian Method Using Marginal Test Statistics

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