Web15 Oct 2024 · Using featureCounts in the Rsubread package I am getting 0 annotations. I started from raw sequencing data and the Refseq genome and Refseq Genomic GTF files … Web17 Oct 2024 · I suggest that you fire up a genome browser (IGV works well) and examine your alignment files. They may need to be sorted and indexed (if subread does not do that automatically). Check to see if your reads are aligning/piling up under exons.
What to do when alignment rate is low even though the genomic …
WebThere I noticed that I get a very low and varying rate of "Successfully assigned alignments" that varies randomly in between either just over 30% or 3-9%. The samples are from human pediatric gliomas. These aren't samples from my institute but samples/data from the ega-archive. Dataset No. 1 paired: yes stranded: yes WebI have 9 files of paired RNA-seq reads from mice. I have aligned them with Rsubread (there is one output .BAM file for each paired-end reads). I am counting with featureCounts. The … introduce disney
featureCounts: 0% assignment - Google Groups
Web2 Oct 2024 · When I run featureCounts it says "Successfully assigned alignments : 0 (0.0%)". I aligned my RNA-seq files to the version 5 b73 Zea mays reference genome … Web30 Jan 2024 · I have ran out of ideas why have I zero alignments in featurecounts, please help. My .gff file looks like this (tac_prodigal.gff) k141_191181_length_270710 … Web8 Nov 2024 · 3.2 Get info on sequencing files. Download SRA info. To link sample info to info sequencing: Go to corresponding SRA page and save the information via the “Send to: File button” This file can also be used to make a script to download sequencing files from the web. Note that sra files can be converted to fastq files via the fastq-dump ... new mom on cell phone