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and how disruption of these processes contributes to congenital heart defects. The project will combine state-of-the-art single-nucleus RNA sequencing, spatial gene expression analysis and molecular
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and how disruption of these processes contributes to congenital heart defects. The project will combine state-of-the-art single-nucleus RNA sequencing, spatial gene expression analysis and molecular
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, but its human burden is badly understood. This PhD addresses this gap, integrating multiple high‑value datasets describing metagenomic and metatranscriptomic sequencing information, clinical and
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