While the amount of small non-coding RNA sequencing data is continuously increasing, it is still unclear to which extent small RNAs are represented in the human genome. Saarland University researchers have analyzed 303 billion sequencing rea

虽然小的非编码RNA测序数据的数量不断增加，但仍然不清楚小RNA在人类基因组中的代表程度。萨尔大学的研究人员已经分析了来自近25,000个数据集的3030亿个测序读数来回答这个问题。

While many cells in our bodies can accumulate oncogenic mutations, the majority of these events do not lead to tumor formation as these abnormal cells are eliminated by defense mechanisms. Instead, tumors arise when a mutation happens in a p

　虽然我们体内的许多细胞可以积累致癌突变，但这些事件中的大多数不会导致肿瘤形成，因为这些异常细胞被防御机制消除。相反，当突变发生在对其特异性敏感的特定细胞类型中时

单细胞mRNA测序(scRNA-seq)允许分析异质细胞群，提供解决各种生物和医学问题的令人兴奋的可能性。最近开发了一系列方法，因此有必要系统地比较它们的灵敏度，准确度，精度和成本效

Single-cell mRNA sequencing (scRNA-seq) allows to profile heterogeneous cell populations, offering exciting possibilities to tackle a variety of biological and medical questions. A range of methods has been recently developed, making it nece

To treat and prevent pregnancy-related disorders, researchers must understand not only what can go wrong, but when. Complications, such as preeclampsia and pre-term birth, often occur in the second or third trimester, and most research to da

为了治疗和预防与妊娠有关的疾病，研究人员不仅要了解可能出现的问题，还要了解何时出错。并发症如先兆子痫和早产，通常发生在妊娠中期或妊娠晚期，迄今为止的大多数研究都集