We're thrilled to announce the return of our RNA-Seq Data Analysis Workshop in March 2024!...
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RNA-Seq Data Analysis Workshop (March 11 - 14, 2024 in Berlin, Germany)
Exciting News from ecSeq Bioinformatics GmbH!
We're thrilled to announce the return of our RNA-Seq Data Analysis Workshop in March 2024!...
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creating GFF file from refernce fasta
HI,
I am working a flatworm for which the reference genome is not well characterized. I found the refernece trancriptome for my species...
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FPKM values differ for sample sample between comparisons?
Hi I have three biological samples (lets call them Sample_A-C)that I want to find DEGs between. Firstly, I'm performing pairwise comparisons between samples...
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RPKM threshold estimation
Dear All,
I have a doubt in the calculation of False postitive rate while checking for FPKM threshold in a RNAseq experiment.
...
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TopHat and mapping QV
Hi,
I'm using TopHat v1.4.1 in order to analyze paired-end reads (75-35) in color space (RNA-Seq analysis).
My tipical command line is:...
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RNAseq quantification - Velvet assembler
Hi
we are using the Velvet assembler plugin in Geneious Server and were able to generate ca. 50,000 contigs from ca. 120 Mio paired reads...
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pileup file symbols "<" and ">"
Hi all,
I have some problems with my pileup file. I used Tophat to map my RNA-seq reads and samtools mpileup to generate my output file....
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A really bad library?
Hi guys,
I am a beginner in the data analysis of experiments RNASeq.
I am currently trying to align reads (36 bp) from an RNASeq experiment...