Transcriptomic data for N. salina CCMP 1776 that had not been previously published, were based on four independent repeats of RNA-seq for normal, nitrogen (N) limitation and high salt stress conditions. The quality of raw reads was evaluated by SolexaQA software v3.1.5 (http://solexaqa.sourceforge.net/) (Cox et al., 2010) and cleaned reads were extracted by removing low-quality (phred < 20) reads from the dataset. The cleaned reads were mapped to the transcripts with the bowtie2 (v2.1.0) software (Langmead et al., 2009). The number of mapped reads for each transcript was calculated and normalized with DESeq package in R (Anders and Huber, 2010). The read counts of all genes were published through the expression menu and genome browse menu on "Nannochloropsis WebDB" (http://web.seeders.co.kr/NSK2019/), and now incorporated into NanDeSyn (http://nandesyn.single-cell.cn/organism/5).
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