Hi all,
I am doing some analysis on the dataset here:
https://trace.ddbj.nig.ac.jp/DRASear...acc=ERX1434776
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All sequence bases have the same quality score.
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Tophat reads kept/discarded during initial conversion
I am using Tophat to analyze illumina HiSeq2000 paired end read data. I have noticed that during the initial execution, Tophat1(and 2) "converts...
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Illumina Reads Quality Control and Preprocessing
Hi,every warm-hearted people in the forum. I am a beginner on genome assembly. I have been using Fastx-toolkit to remove the reads that have less than...