Hi all,
While doing QC preprocessing of RNA-seq reads, what could be the minumum length of reads for a reliable assembly: reference-base or de novo assembly?
I am a greenhand in RNA-seq area, and just wonder, when we met bad quality data, to what extent could we trim the reads?
for example, as fastqc results shown in the attachment.
Do I have to trim the first 10bps and the last 20bps?
Is 50bps left enough for (tophat->cufflinks) assembly?
Thank you very much in advance!!!!!!
While doing QC preprocessing of RNA-seq reads, what could be the minumum length of reads for a reliable assembly: reference-base or de novo assembly?
I am a greenhand in RNA-seq area, and just wonder, when we met bad quality data, to what extent could we trim the reads?
for example, as fastqc results shown in the attachment.
Do I have to trim the first 10bps and the last 20bps?
Is 50bps left enough for (tophat->cufflinks) assembly?
Thank you very much in advance!!!!!!
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