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- 9 months ago
Posts by javiersg
... Good morning Jennifer. That is the showed print by *fastq groomer* Groomed 18487694 sanger reads into sanger reads. Based upon quality and sequence, the input data is valid for: sanger Input ASCII range: '5'(53) - 'J'(74) Input decimal range: 20 - 41 I guess that the sequences are ...
... Good morning everyone My trinity analysis is stucked before to start. I wonder what is the hipothetical problem. The files are fastqc which was filtered before. The error insisted if my files are sra format. But I think that is a fastq format. Someone can give a clue to me. **The file: Encoding ...
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