I saved the reads in a FASTQ file.
我把测序读段保存到了一个 FASTQ 文件里。
After trimming adapters, we aligned the FASTQ reads to the reference genome and filtered low-quality bases using the quality scores.
去除接头序列后,我们将 FASTQ 读段比对到参考基因组,并利用质量分数过滤掉低质量的碱基。
《Bioinformatics Data Skills: Reproducible and Robust Research with Open Source Tools》(涉及 FASTQ、FASTA 等常用数据格式与处理流程)
《RNA-seq Data Analysis: A Practical Approach》(常用 FASTQ 作为 RNA 测序原始数据输入格式)
Cock, P. J. A., et al. “The Sanger FASTQ file format for sequences with quality scores, and the Solexa/Illumina FASTQ variants.” Nucleic Acids Research(讨论 FASTQ 及其变体与质量分数编码)