Jiaqi Huang

ORCID: 0000-0002-9006-2453
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Research Areas
  • Cancer Genomics and Diagnostics
  • Advanced Energy Technologies and Civil Engineering Innovations
  • RNA modifications and cancer
  • Antifungal resistance and susceptibility
  • Genomics and Phylogenetic Studies
  • Genomic variations and chromosomal abnormalities
  • Lung Cancer Treatments and Mutations
  • interferon and immune responses
  • Lung Cancer Research Studies
  • Ovarian cancer diagnosis and treatment
  • Cancer-related molecular mechanisms research
  • Drug Solubulity and Delivery Systems
  • Ferroptosis and cancer prognosis
  • Plant Pathogens and Fungal Diseases
  • Probiotics and Fermented Foods
  • Single-cell and spatial transcriptomics
  • Hydrogels: synthesis, properties, applications
  • Vasculitis and related conditions
  • IL-33, ST2, and ILC Pathways
  • Neutrophil, Myeloperoxidase and Oxidative Mechanisms
  • Metal complexes synthesis and properties
  • Mycotoxins in Agriculture and Food
  • Autonomous Vehicle Technology and Safety
  • Complement system in diseases
  • RNA Research and Splicing

National Institutes for Food and Drug Control
2023-2024

Peking University
2024

Peking University Third Hospital
2024

China Pharmaceutical University
2024

Southern Medical University
2024

Soochow University
2016-2023

Beijing Institute of Nanoenergy and Nanosystems
2020-2021

Tsinghua University
2021

South China University of Technology
2020

Xiamen University
2018

Presented here is a genome sequence of an individual human. It was produced from ∼32 million random DNA fragments, sequenced by Sanger dideoxy technology and assembled into 4,528 scaffolds, comprising 2,810 bases (Mb) contiguous with approximately 7.5-fold coverage for any given region. We developed modified version the Celera assembler to facilitate identification comparison alternate alleles within this diploid genome. Comparison National Center Biotechnology Information human reference...

10.1371/journal.pbio.0050254 article EN cc-by PLoS Biology 2007-08-31
William C. Nierman Arnab Pain Michael J. Anderson Jennifer R. Wortman Sun Kim and 93 more Javier Arroyo Matthew Berriman Keietsu Abe David B. Archer Clara Bermejo Joan W. Bennett Paul Bowyer Dan Chen Matthew Collins Richard Coulsen Robert M. Davies Paul S. Dyer Mark Farman Nadia Fedorova Natalie D. Fedorova Tamara V. Feldblyum Rainer Fischer Nigel Fosker Audrey Fraser José L. Garcı́a Maria J. García Arlette Goble Gustavo H. Goldman Katsuya Gomi Sam Griffiths‐Jones Ryan Gwilliam Brian J. Haas Hubertus Haas David Harris Hiroyuki Horiuchi Jiaqi Huang Sean Humphray Javier Jiménez Nancy P. Keller Hoda Khouri Katsuhiko Kitamoto Tetsuo Kobayashi Sven Konzack Resham Kulkarni Toshitaka Kumagai Anne Lafton Jean‐Paul Latgé Weixi Li Angela Lord Charles Lu William H. Majoros Gregory S. May Bruce L. Miller Yasmin A. Mohamoud Marı́a Molina Michel Monod Isabelle Mouyna Stephanie Mulligan Lee Murphy Susan O’Neil Ian T. Paulsen Miguel Á. Peñalva Mihaela Pertea Claire Price Bethan Pritchard Michael A. Quail Ester Rabbinowitsch Neil Rawlins Marie-Adele Rajandream Utz Reichard Hubert Renauld Geoffrey D. Robson Santiago Rodrı́guez de Córdoba José M. Rodríguez-Peña Catherine M. Ronning Simon Rutter Steven L. Salzberg Miguel Sánchez Juan C. Sánchez-Ferrero David Saunders Kathy Seeger Rob Squares Steven Squares Michio Takeuchi Fredj Tekaia Geoffrey Turner Carlos R. Vázquez de Aldana Janice F. Weidman Owen White John R. Woodward Jae‐Hyuk Yu Claire M. Fraser James E. Galagan Kiyoshi Asai Masayuki Machida Neil Hall Bart Barrell David W. Denning

10.1038/nature04332 article EN Nature 2005-12-21

There is much interest in characterizing the variation a human individual, because this may elucidate what contributes significantly to person's phenotype, thereby enabling personalized genomics. We focus here on variants 'exome,' which set of exons genome, exome believed harbor functional variation. provide an analysis ∼12,500 that affect protein coding portion individual's genome. identified ∼10,400 nonsynonymous single nucleotide polymorphisms (nsSNPs) ∼15–20% are rare population. predict...

10.1371/journal.pgen.1000160 article EN cc-by PLoS Genetics 2008-08-14

Small cell lung cancer (SCLC) is an aggressive disease with poor survival. A few sequencing studies performed on limited number of samples have revealed potential disease-driving genes in SCLC, however, much still remains unknown, particularly the Asian patient population. Here we conducted whole exome (WES) and transcriptomic primary tumors from 99 Chinese SCLC patients. Dysregulation tumor suppressor TP53 RB1 was observed 82% 62% patients, respectively, more than half patients (62%)...

10.1371/journal.pgen.1005895 article EN cc-by PLoS Genetics 2016-04-19

Chinese lung cancer patients have distinct epidemiologic and genomic features, highlighting the presence of specific etiologic mechanisms other than smoking. Here, we present a comprehensive landscape 149 non-small cell (NSCLC) cases identify 15 potential driver genes. We reveal that are specially characterized by not only highly clustered EGFR mutations but mutational signature (MS3, 33.7%), is associated with inflammatory tumor-infiltrating B lymphocytes (P = 0.001). The mutation rate...

10.1038/s41467-018-04492-2 article EN cc-by Nature Communications 2018-05-20

Sodium Sulfobutylether-β-cyclodextrin (SBE-β-CD) is a derivative of β-cyclodextrin, characterized by its stereo structure, which closely resembles truncated cone with hydrophobic internal cavity. The solubility insoluble substances within the cavity significantly enhanced, reducing contact between guest and environment. Consequently, SBE-β-CD frequently employed as co-solvent stabilizer. As research progresses, it has been observed that inclusion reversible competitive. Besides, some...

10.1016/j.carbpol.2024.121985 article EN cc-by-nc Carbohydrate Polymers 2024-02-24

It is now clear that tyrosine kinases represent attractive targets for therapeutic intervention in cancer. Recent advances DNA sequencing technology provide the opportunity to survey mutational changes cancer a high-throughput and comprehensive manner. Here we report on sequence analysis of members receptor kinase (RTK) gene family genomes glioblastoma brain tumors. Previous studies have identified number molecular alterations glioblastoma, including amplification RTK epidermal growth factor...

10.1073/pnas.0507200102 article EN Proceedings of the National Academy of Sciences 2005-09-26

The scraper conveyor plays the role of bearing, coal, shearer guiding and hydraulic support in fully mechanized mining face, is "backbone" whole set equipment. Its performance, reliability life are important guarantee for normal production face good technical economic results. As one most components central groove, choice materials overall wear resistance play a vital conveyor. middle groove mainly as running track chain, channel coal load. In actual use process, damage rate gang plate very...

10.1049/icp.2024.4189 article EN IET conference proceedings. 2025-01-01

Background Sepsis is a common critical condition that can lead to multiple organ injury. Sepsis-induced acute respiratory distress syndrome (ARDS) frequently an important cause of poor prognosis and associated with high mortality rates, despite existing therapeutic interventions. Neutrophil infiltration extracellular traps (NET) are implicated in lung injury (ALI) ARDS following sepsis. As circulating neutrophils infiltrate infected tissues, they come into direct contact vascular endothelial...

10.3389/fimmu.2025.1548913 article EN cc-by Frontiers in Immunology 2025-03-28

It is difficult to detect the nighttime lane lines which showed darker and uneven lighted. In order overcome these problems, a recognition method was proposed. Firstly, edge enhancement based on Laplacian used enhance pre-processing image's edges. Then, edges were detected by Canny Otsu algorithm straight within one third at bottom of image Hough transform. Finally, an inside line extraction proposed basis slope constraint. Thereby, aim marking realized. By experimenting with various...

10.1109/rcar.2016.7784064 article EN 2022 IEEE International Conference on Real-time Computing and Robotics (RCAR) 2016-06-01

Studies already revealed that some E3 ubiquitin ligases participated in the immune response after viral infection by regulating type I interferon (IFN) pathway. Here, we demonstrated signaling enhanced translocation of ETS1 to nucleus and promoter activity ligase DTX3L (deltex 3L) virus thus increased expression DTX3L. Further experiments suggested ubiquitinated TBK1 at K30 K401 sites on K63-linked ubiquitination was also necessary for mediating phosphorylation through binding with tyrosine...

10.1128/jvi.00687-23 article EN Journal of Virology 2023-05-31

TGF-β-centered epithelial-mesenchymal transition (EMT) is a key process involved in radiation-induced pulmonary injury (RIPI) and fibrosis. PIEZO1, mechanosensitive calcium channel, expressed myeloid cell has been found to play an important role bleomycin-induced Whether PIEZO1 related with EMT remains elusive. Herein, we that functional rat primary type II epithelial cells RLE-6TN cells. After irradiation, expression was increased lung alveolar line, which accompanied changes evidenced by...

10.3389/fmolb.2021.725275 article EN cc-by Frontiers in Molecular Biosciences 2021-10-13

Abstract Long non-coding RNAs (lncRNAs) play a crucial role in macrophage development but little is known about their asthma. Here, we investigated the of lncRNA lncTRPM2-AS asthma and found that participates promotion inflammation. Downregulation promoted apoptosis inhibited proliferation production cytokines including IL-1β, IL-4, IL-6, IL-10, TNF-α, TGF-β. RNA-immunoprecipitation mass spectrometry indicated protein TRPM2 interacted with both E3 ubiquitin ligase TRIM21. LncTRPM2-AS...

10.1038/s41419-021-04437-6 article EN cc-by Cell Death and Disease 2021-12-13

An aquo-cisplatin arsenite multidrug nanocomposite loaded with cisplatin and arsenic trioxide prodrugs was reported for overcoming drug resistance combination therapy.

10.1039/c8bm01039k article EN Biomaterials Science 2018-11-08

We tested the hypothesis that co-coordinated up-regulation or down-regulation of several ovarian cell surface kinases may provide clues for better understanding disease and help in rational design therapeutic targets.We compared expression signature 69 normal epithelial cells (OSE), with OSE from patients at high risk cancer.Seven kinases, ALK, EPHA5, EPHB1, ERBB4, INSRR, PTK, TGFbetaR1 displayed a distinctive linear trend normal, highrisk, malignant epithelium. confirmed these results using...

10.1593/tlo.09199 article EN cc-by-nc-nd Translational Oncology 2009-12-01

Tumors are characterized by properties of genetic instability, heterogeneity, and significant oligoclonality. Elucidating this intratumoral heterogeneity is challenging but important. In study, we propose a framework, BubbleTree, to characterize the tumor clonality using next generation sequencing (NGS) data. BubbleTree simultaneously elucidates complexity biopsy, estimating cancerous cell purity, ploidy, allele-specific copy number, represents in an intuitive graph. We further developed...

10.1093/nar/gkv1102 article EN cc-by Nucleic Acids Research 2015-11-17

Cell-free DNA (cfDNA) is gaining substantial attention from both biological and clinical fields as a promising marker for liquid biopsy. Many aspects of disease-related features have been discovered cfDNA high-throughput sequencing (HTS) data. However, there still lack integrative systematic tools HTS data analysis quality control (QC).Here, we propose cfDNApipe, an easy-to-use python package whole-genome (WGS) bisulfite (WGBS) analysis. It covers the entire pipeline data, including raw...

10.1093/bioinformatics/btab413 article EN cc-by-nc Bioinformatics 2021-05-26

Abstract The MAT-C1 subline of the 13762 rat mammary adenocarcinoma has highly stable, branched microvilli and immobile cell surface receptors. A membrane- microfilament-associated 58-kDa protein (p58) in been implicated stabilization microfilament-membrane interactions. This is associated with a high M(r) glycoprotein complex containing (proto)oncogene p185neu other signal transduction components putative particle. Amino acid sequences were obtained from two trypsin peptides p58. Screening...

10.1016/s0021-9258(17)36575-4 article EN cc-by Journal of Biological Chemistry 1994-05-01
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