I'm a newbie and I'd like to know how to start doing analysis of multiplexed 454 data. I know its wide question but I really don't know where to start?
check out the mothur package, it has 454 flow trimming and demultiplexing features that are very handy and usable even if your data has nothing to do with metagenomics
I have a GEO accession number from a longitudinal study following severe malaria patient who then became mild case. I want to compare their transcription …
Dear all, I'm new in fungal ITS (internal transcribed spacer) metabarcoding analysis, so please ask if you don't understand my question. Our lab received Illumina …
<p>Hi everybody,</p> <p>I am displaying the genes and exons of a GFF file with this module. However, I'd like to connect the corresponding exons, but …
<p>Can anybody please suggest some good resources (guides, tutorials, online courses, books...) for NGS pipelines and workflows? I'm interested in both RNA-seq and ChIP-seq but, …
<p>I'd like to align my trimmed 454 metagenomic reads to a reference sequence and generate plots of the coverage / percent identity / recruitment.</p> <p>Both …
Do, or do not. There is no try. :)
Your sequencing provider should demultiplex the data for you, assuming you used the standard Roche MID barcode system.