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RNA-Seq reveals the extent of small RNAs representation in t

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

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RNA-Seq揭示了人類基因組中小RNA表達的程度

雖然小的非編碼RNA測序數據的數量不斷增加，但仍然不清楚小RNA在人類基因組中的代表程度。薩爾大學的研究人員已經分析了來自近25,000個數據集的3030億個測序讀數來回答這個問題。

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Single cell sequencing sheds light on why cancers form in sp

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

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單細胞測序揭示了癌癥在特定細胞類型中形成的

雖然我們體內的許多細胞可以積累致癌突變，但這些事件中的大多數不會導致腫瘤形成，因為這些異常細胞被防御機制消除。相反，當突變發生在對其特異性敏感的特定細胞類型中時

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單細胞RNA測序方法的比較分析

單細胞mRNA測序(scRNA-seq)允許分析異質細胞群，提供解決各種生物和醫學問題的令人興奮的可能性。最近開發了一系列方法，因此有必要系統地比較它們的靈敏度，準確度，精度和成本效

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Comparative analysis of single-cell RNA-sequencing methods

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

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Single-cell RNA-Seq of cells in the early human placenta may

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

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早期人胎盤中的單細胞RNA-Seq細胞可以揭示問題懷

為了治療和預防與妊娠有關的疾病，研究人員不僅要了解可能出現的問題，還要了解何時出錯。并發癥如先兆子癇和早產，通常發生在妊娠中期或妊娠晚期，迄今為止的大多數研究都集

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