Live Example在线示例

Yeast SNF2 de novo RNA-seq standard reportYeast SNF2 无参 RNA-seq 标准流程报告

A 24-sample no-reference example generated by rnaseq-standard-flow 0.2.0-r2 and collected by rnaseq-report-flow 0.2.0-r2. It starts from FASTQ, assembles a transcriptome, quantifies against the assembled transcripts, annotates transcripts through homology, and then continues through DE, enrichment, and reporting.

这是由 rnaseq-standard-flow 0.2.0-r2 生成、由 rnaseq-report-flow 0.2.0-r2 收集的 24 样本无参示例。它从 FASTQ 出发,先组装转录组,再基于组装转录本定量,通过同源信息注释转录本,随后继续完成差异表达、功能富集和报告生成。

24samples样本
9609filtered transcripts过滤后转录本
713significant features显著特征
5705GO gene setsGO 基因集

What this no-reference example demonstrates

这个无参示例展示了什么

The de novo route answers a different question from the reference route. Instead of asking how reads support known genes in a known annotation, it asks whether a usable transcriptome can be assembled from the reads, how much each assembled transcript is expressed, and which transcript-level features change between WT and SNF2KO samples.

无参路线回答的问题和有参路线不同。它不是直接问 reads 如何支持已知注释中的基因,而是先问能否从 reads 组装出可用转录组,再问每个组装转录本表达量如何,以及 WT 与 SNF2KO 之间哪些转录本层面特征发生变化。

Sample correlation heatmap from the de novo report

Sample correlation样本相关性

PCA plot from the de novo report

PCA structurePCA 样本结构

Enrichment dotplot from the de novo report

Annotation-derived enrichment注释派生富集

Run summary

运行摘要

  • Analysis mode: de novo / no-reference分析模式:无参 / no-reference
  • DE source: de novo transcript counts差异分析来源:无参转录本计数
  • Average Salmon reads: 457133.12平均 Salmon reads:457133.12
  • De novo N50: 1308无参转录本 N50:1308
  • BUSCO: skipped in this runBUSCO:本次运行跳过

Included artifacts

包含内容

The report collector found 6 modules, 108 collected files, 54 tables, 28 plot files, and 26 linked HTML reports. The feature space is transcript-level unless an explicit tx2gene or cluster mapping is supplied.

报告收集器发现 6 个模块、108 个收集文件、54 个表格、28 个图文件和 26 个 HTML 子报告链接。除非显式提供 tx2gene 或聚类映射,否则这里的特征空间是转录本层面。