纳米孔测序
计算机科学
计算生物学
RNA序列
软件
数据挖掘
DNA测序
参考基因组
转录组
生物
遗传学
基因
基因表达
程序设计语言
作者
Tommaso Leonardi,Adrien Léger
出处
期刊:Methods in molecular biology
日期:2021-01-01
卷期号:: 569-578
被引量:4
标识
DOI:10.1007/978-1-0716-1307-8_31
摘要
The recent advent of Nanopore sequencing allows for the sequencing of full-length RNA or cDNA molecules. This new type of data introduces new challenges from the computational point of view, and requires new software as well as dedicated analysis pipelines. In this chapter, we guide the reader through the typical analysis steps required to process the raw data produced by the instrument into a table of counts suitable for downstream analyses. We first describe the procedure to convert raw direct RNA-Seq and cDNA-Seq data into sequences in fastq format. We then outline how to perform quality control and filtering steps and how to map the filtered long reads to a reference transcriptome or genome.
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