scanpy单细胞分析流程

最新推荐文章于 2024-05-17 09:19:42 发布

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最新推荐文章于 2024-05-17 09:19:42 发布

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分类专栏： Bioinformation 文章标签： python 人工智能算法

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梳理一下scanpy单细胞分析流程（处理的是scRNA-seq）。

先上一张流程图：
在这里插入图片描述

scanpy单细胞分析流程

import scanpy as sc

Read data

常用的文件格式有两种，分别是h5ad和10X mtx

# read h5ad
adata = sc.read()

# read 10X mtx
adata = read_10x_mtx()

Preprocessing

QC

QC这一步目标是过滤掉低质量的细胞和基因

我们通常可以通过以下指标进行QC

Cell counts
UMI counts per cell
Genes detected per cell
Complexity(novelty score)
Mitochondrial counts ratio

Cell counts

这个指标可以与预期的细胞数进行对比，用来判断是否有垃圾细胞存在。需要注意的是，

UMI counts per cell

UMI（unique molecular identifiers），用来给mRNA计数

The UMI counts per cell should generally be above 500, that is the low end of what we expect. If UMI counts are between 500-1000 counts, it is usable but the cells probably should have been sequenced more deeply.

Genes detected per cell

每个细胞表达的基因数，在scanpy的教程中，过滤掉了低于200的细胞

novelty score

什么是novelty score

We can evaluate each cell in terms of how complex the RNA species are by using a measure called the novelty score. The novelty score is computed by taking the ratio of nGenes over nUMI. If there are many captured transcripts (high nUMI) and a low number of genes detected in a cell, this likely means that you only captured a low number of genes and simply sequenced transcripts from those lower number of genes over and over again. These low complexity (low novelty) cells could represent a specific cell type (i.e. red blood cells which lack a typical transcriptome), or could be due to an artifact or contamination. Generally, we expect the novelty score to be above 0.80 for good quality cells.

novelty score公式

This value is quite easy to calculate, as we take the log10 of the number of genes detected per cell and the log10 of the number of UMIs per cell, then divide the log10 number of genes by the log10 number of UMIs. The novelty score and how it relates to complexity of the RNA species, is described in more detail later in this lesson.

Mitochondrial counts ratio

This metric can identify whether there is a large amount of mitochondrial contamination from dead or dying cells. We define poor quality samples for mitochondrial counts as cells which surpass the 0.2 mitochondrial ratio mark, unless of course you are expecting this in your sample.

在scanpy中，这一值被设定为5%

合理的值范围可能是5%—20%

Joint filtering effects

Considering any of these QC metrics in isolation can lead to misinterpretation of cellular signals. For example, cells with a comparatively high fraction of mitochondrial counts may be involved in respiratory processes and may be cells that you would like to keep. Likewise, other metrics can have other biological interpretations. A general rule of thumb when performing QC is to set thresholds for individual metrics to be as permissive as possible, and always consider the joint effects of these metrics. In this way, you reduce the risk of filtering out any viable cell populations.

Two metrics that are often evaluated together are the number of UMIs and the number of genes detected per cell. Here, we have plotted the number of genes versus the number of UMIs coloured by the fraction of mitochondrial reads. Jointly visualizing the count and gene thresholds and additionally overlaying the mitochondrial fraction, gives a summarized persepective of the quality per cell.
在这里插入图片描述
Good cells will generally exhibit both higher number of genes per cell and higher numbers of UMIs (upper right quadrant of the plot). Cells that are poor quality are likely to have low genes and UMIs per cell, and correspond to the data points in the bottom left quadrant of the plot. With this plot we also evaluate the slope of the line, and any scatter of data points in the bottom right hand quadrant of the plot. These cells have a high number of UMIs but only a few number of genes. These could be dying cells, but also could represent a population of a low complexity celltype (i.e red blood cells).