WebApr 1, 2014 · featureCounts: an efficient general purpose program for assigning sequence reads to genomic features. featureCounts is available under GNU General Public … WebMar 17, 2024 · Details. featureCounts is a general-purpose read summarization function that can assign mapped reads from genomic DNA and RNA sequencing to genomic features or meta-features.. The function takes as input a set of SAM or BAM files containing read mapping results. The files might be generated by align or subjunc or any suitable …
featureCounts: an efficient general purpose program for …
WebThis optional argument can be used with '-J' option to improve read counting for junctions. # Parameters specific to paired end reads. -p. If specified, fragments (or templates) will be counted instead of reads. This option is only applicable for paired-end reads; single-end reads are always counted as reads. -B. WebMay 8, 2024 · featuresCounts软件用于统计基因/转录本上mapping的reads数,也就是用于raw count定量。该软件不仅支持基因/转录本的定量,也支持exon, gene bodies, genomic … imdb last ounce of courage
featureCounts的MultiQC结果解读 - 腾讯云开发者社区-腾讯云
WebFeb 2, 2024 · featureCounts的结果一共有两个部分,General Stats和featureCounts。 General Stats. 在此部分,我们能直观的看到每个样本有多少reads单一比对到基因注释 … WebApr 1, 2014 · Results: We present featureCounts, a read summarization program suitable for counting reads generated from either RNA or genomic DNA sequencing experiments. featureCounts implements highly efficient chromosome hashing and feature blocking techniques. It is considerably faster than existing methods (by an order of magnitude for … WebApr 9, 2024 · featureCounts(subread) v2.0.1; 使用说明 安装featureCounts 该工具属于Subread软件中的定量工具,另外subread还可以进行比对和寻找SNP位点,在这里就不 … list of mayo clinics