More posts like this
-
RNA-seq assigned alignments
written by Manko47 •Hey everyone, I've a rather technical question regarding assigned alignments percentage to human genome (GRCh38.p14) - I'm using Gencode v47 version along it's annotation. My …
-
Newer Tools for Alternative Splicing?
written by rohit.aita •Hi everyone, I've been working with rna-seq to analyze genome wide alternative splicing and was wondering if there are newer tools besides rMATS, SUPPA, and …
-
best practices/ pipeline for miRNA sequencing QC
written by RNAseqerI'm currently searching the literature for a recent 'best practices' review of miRNA sequencing data QC. I was wondering if there was a pipeline which …
-
Why are there many reads with green color in IGV of RNA-seq data?
written by ApprenticeHi. I'm analyzing RNA-seq data. I did a mapping of RNA-seq data to the reference sequence (hg19) and got a bam file. To confirmed mapped …
-
Fusion sequence matching
written by pennakizaHello everyone, I was wondering if it would make any sense to detect gene fusions in my RNA seq data by just matching the sequence …
-
mapping rate of small rna-seq with different references
written by woongjaej •Hi, folks I'm new to analysing small RNa-seq and I have some questions. Hope some experts analysing small RNA-seq could give me some advices. 1. …
-
RNA Seq data network analysis
written by chetana •Hi everyone, I'm relatively new to RNA-Seq data analysis. I was wondering if there are any software or tools out there to get the network …
-
Per sequence GC content fail linked to rRNA ?
written by cjmb3 •Hi everyone, I'm new to RNA-seq and I'm struggling with the QC of my data. I performed Illumina paired-end stranded RNA-seq on human cells (ran …
-
microRNA microarray or small RNASeq
written by syrez •Hi all! Recently, we were given a choice between microRNA microarray OR small RNASeq for mouse. Upon further discussion, someone raised a question if mouse …
-
Should Rna-Seq Reads Map To One Strand Of Cdna Reference?
written by chjiao3456 •<p>Hi everyone, I'm mapping mRNA-seq data (single end, 40bp) of C.elegans to the cDNA reference (junction of exons) with bowtie, I'm a beginner for RNA-seq …
Where is your sample coming from? Is there a possibility of contamination? If yes, from which source.
The samples are from patients and were checked for contamination with none found. Thank you for your help!
While the percentage can be much higher you have what you have. Are you using a splice-aware aligner? You can take a look at the reads that did not map by checking a few with blast @NCBI (unless you have already done this by "were checked for contamination").