Publications by authors named "Jingyao Zeng"

The field of single-cell RNA sequencing (scRNA-seq) has advanced rapidly in the past decade, generating significant amounts of valuable data for researchers to study complex tumor profiles. This data is crucial for gaining innovative insights into cancer biology. CancerSCEM (https://ngdc.

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Article Synopsis
  • Single-cell transcriptome-wide association studies (scTWAS) is a cutting-edge method that enhances gene-trait association analysis by focusing on cellular precision and addressing issues of cell-type diversity inherent in traditional TWAS.
  • The scTWAS Atlas is a new comprehensive database that compiles over 2.7 million gene-trait associations linked to various traits and cell types, featuring tools for data visualization and multi-omics regulatory network construction.
  • This user-friendly platform facilitates in-depth exploration of genetic mechanisms within specific cell types, providing valuable insights for research related to human health and biological processes.
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Cardiovascular disease (CVD) is the leading cause of illness and death worldwide. Numerous studies have been conducted into the underlying mechanisms and molecular characteristics of CVD using various omics approaches. However, there is still a need for comprehensive resources on CVD.

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Al impurity is among the most likely components to enter the spent lithium-ion battery (LIB) cathode powder due to the strong adhesion between the cathode material and the Al current collector. However, high-value metal elements tend to be lost during the deep removal of Al impurities to obtain high-purity metal salt products in the conventional hydrometallurgical process. In this work, the harmful Al impurity is designed as a beneficial ingredient to upcycle high-voltage LiCoO by incorporating robust Al-O covalent bonds into the bulk of the cathode assisted with Ti modification.

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Pan-genome studies are important for understanding plant evolution and guiding the breeding of crops by containing all genomic diversity of a certain species. Three short-read-based strategies for plant pan-genome construction include iterative individual, iteration pooling, and map-to-pan. Their performance is very different under various conditions, while comprehensive evaluations have yet to be conducted nowadays.

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NaFe(PO)(PO) (NFPP) is currently drawing increased attention as a sodium-ion batteries (SIBs) cathode due to the cost-effective and NASICON-type structure features. Owing to the sluggish electron and Na conductivities, however, its real implementation is impeded by the grievous capacity decay and inferior rate capability. Herein, multivalent cation substituted microporous NaFeAl(PO)(PO) (NFAPP) with wide operation-temperature is elaborately designed through regulating structure/interface coupled electron/ion transport.

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Cancer cell lines are essential in cancer research, yet accurate authentication of these cell lines can be challenging, particularly for consanguineous cell lines with close genetic similarities. We introduce a new Cancer Cell Line Hunter (CCLHunter) method to tackle this challenge. This approach utilizes the information of single nucleotide polymorphisms, expression profiles, and kindred topology to authenticate 1389 human cancer cell lines accurately.

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Genome-wide association study has identified fruitful variants impacting heritable traits. Nevertheless, identifying critical genes underlying those significant variants has been a great task. Transcriptome-wide association study (TWAS) is an instrumental post-analysis to detect significant gene-trait associations focusing on modeling transcription-level regulations, which has made numerous progresses in recent years.

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Diabetes is associated with higher prevalence of cognitive dysfunction, while the underlying mechanism is still elusive. In this study, we aim to explore the potential mechanism of diabetes-induced cognitive dysfunction and assess the therapeutic effects of Gastrodin on cognitive dysfunction. Diabetes was induced by a single injection of streptozotocin.

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Background: Uveal melanoma (UM) is the most common intraocular malignancy in adults, with a poor survival prognosis. To date, limited understanding of UM's molecular mechanisms constitutes an obstacle to developing effective therapy. In this study, we examined key regulators mediating UM progression and their clinical relevance.

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Article Synopsis
  • Transcriptome-wide association studies (TWASs) help identify links between genes and traits, improving our understanding of genetic influences on diseases.
  • TWAS Atlas is a new online knowledgebase that compiles over 400,000 gene-trait associations from various studies, covering a wide range of genes and traits.
  • The platform features an interactive knowledge graph and a user-friendly interface, making it easy for researchers to access and explore TWAS data for insights into health and disease.
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Somatic variants act as critical players during cancer occurrence and development. Thus, an accurate and robust method to identify them is the foundation of cutting-edge cancer genome research. However, due to low accessibility and high individual-/sample-specificity of the somatic variants in tumor samples, the detection is, to date, still crammed with challenges, particularly when lacking paired normal samples as control.

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With the proliferating studies of human cancers by single-cell RNA sequencing technique (scRNA-seq), cellular heterogeneity, immune landscape and pathogenesis within diverse cancers have been uncovered successively. The exponential explosion of massive cancer scRNA-seq datasets in the past decade are calling for a burning demand to be integrated and processed for essential investigations in tumor microenvironment of various cancer types. To fill this gap, we developed a database of Cancer Single-cell Expression Map (CancerSCEM, https://ngdc.

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LiMn O (LMO) cathodes suffer from limited cycle life, resulting from Mn dissolution and side reactions between electrode and electrolyte. In this study, Sr-modified LMO is prepared by using a simple strategy. The nature and position of large-radius Sr ions are investigated, alongside their influence on the structural stability of the bulk.

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Genotype imputation is a statistical method for estimating missing genotypes from a denser haplotype reference panel. Existing methods usually performed well on common variants, but they may not be ideal for low-frequency and rare variants. Previous studies showed that the population similarity between study and reference panels is one of the key factors influencing the imputation accuracy.

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  • China National Center for Bioinformation (CNCB) launched the 2019 Novel Coronavirus Resource (2019nCoVR) on January 22, 2020, as an open-access platform providing comprehensive sequence and clinical data for SARS-CoV-2.
  • The resource includes detailed statistics and quality evaluations of all SARS-CoV-2 isolates, allowing researchers to visualize genomic variations and track their evolution over time through historical haplotype maps.
  • Additionally, 2019nCoVR aggregates relevant literature and supports data submissions, ensuring daily updates to aid the global research community in understanding COVID-19.
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Functionalized ionic liquids (FILs) based on vegetable oils have been directly synthesized and used for the first time to extract rare earth elements (REEs). Carbon dioxide gas is introduced to successfully strip REE-loaded FILs in the presence of water. The novel extraction process reveals some advantages of accessibility, biocompatibility and sustainability as well as cost efficiency.

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Precision medicine calls upon deeper coverage of population-based sequencing and thorough gene-content and phenotype-based analysis, which lead to a population-associated genomic variation map or database. The Chinese Genomic Variation Database (CGVD; https://bigd.big.

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  • The CASPMI project by the Chinese Academy of Sciences has created a new northern Han reference genome (NH1.0) to assist in understanding genetic diseases and traits specific to China, using advanced sequencing technologies.
  • The NH1.0 genome was constructed by analyzing 597 healthy individuals and yielded millions of genetic variations, including notable findings related to waist circumference and genetic diversity between northern and southern populations.
  • The study offers valuable insights for personalized medicine, highlighting the importance of geographic genetic differences and suggesting specific genetic markers that could affect health in different regions.
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Coconut (Cocos nucifera L.), a member of the palm family (Arecaceae), is one of the most economically important crops in tropics, serving as an important source of food, drink, fuel, medicine, and construction material. Here we report an assembly of the coconut (C.

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Transcripts are expressed spatially and temporally and they are very complicated, precise and specific; however, most studies are focused on protein-coding related genes. Recently, massively parallel cDNA sequencing (RNA-seq) has emerged to be a new and promising tool for transcriptome research, and numbers of non-coding RNAs, especially lincRNAs, have been widely identified and well characterized as important regulators of diverse biological processes. In this study, we used ultra-deep RNA-seq data from 15 mouse tissues to study the diversity and dynamic of non-coding RNAs in mouse.

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Recently, RNA-seq has become widely used technology for transcriptome profiling due to its single-base accuracy and high-throughput speciality. In this study, we applied a computational approach on an integrated RNA-seq dataset across 15 normal mouse tissues, and consequently assigned 8408 house-keeping (HK) genes and 2581 tissue-specific (TS) genes among UCSC RefGene annotation. Apart from some basic genomic features, we also performed expression, function and pathway analysis with clustering, DAVID and Ingenuity Pathway Analysis, indicating the physiological connections (tissues) and diverse biological roles of HK genes (fundamental processes) and TS genes (tissue-corresponding processes).

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