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Field
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The Taikang Center for Life and Medical Sciences at Wuhan University invites applications for faculty positions at multiple levels. As an independently operated research institute under Wuhan
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bioinformatic tools (FASTQC, Stacks, Geneious or similar). Conduct sequence alignment, assembly and SNP filtering to generate data matrices suitable for phylogenetic and population-genomic analyses. Support
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Zhejiang University (ZJU), founded in 1897, ranks among the top 3 on Chinese mainland and within the top 100 in the Times Higher Education World Reputation Ranking and QS World University Rankings. The Stomatology Hospital，School of Stomatology, Zhejiang University School of Medicine (ZJUSS) was...
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/Qualifications Responsible for bioinformatic data analysis in the research group's projects. Sequencing, analysis, and interpretation of genetic variants, fusion genes, and expression profiles identified by NGS
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) molecular biology (DNA extraction, PCR, sample preparation for sequencing); and 3) preliminary bioinformatics processes of short sequences (e.g., alignments, taxonomy, species delimitation). Years of Research
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managing communication projects with multiple stakeholders and channels. Knowledge of the biomedical research ecosystem and of public and private funding mechanisms. Strategic vision and ability to align
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-discrimination. Our values are aligned with the Sustainable Development Goals, the 2030 Agenda and the Corporate Social Responsibility policy of the Hospital Universitario La Paz, within whose scope the Foundation
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at the intersection of computational biology, immunogenomics, and cancer biology. The successful candidate will play a key role in co-leading the analysis of single-cell and bulk RNA sequencing data across multiple
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mechanistic insight in the role of large-scale chromosomal changes. The successful candidate will play a key role in co-leading the analysis of genomic DNA, single-cell and bulk RNA sequencing data across
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RNA from haematological samples. - Molecular characterisation of cell lines derived from haematological neoplasms using next-generation sequencing (NGS) techniques and the development of in vitro