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SEQanswers June Challenge Has Begun!

The competition has begun! We're giving away a $50 Amazon gift card to the member who answers the most questions on our site during the month. We want to encourage our community members to share their knowledge and help each other out by answering questions related to sequencing technologies, genomics, and bioinformatics. The competition is open to all members of the site, and the winner will be announced at the beginning of July. Best of luck!

For a list of the official rules, visit (https://www.seqanswers.com/forum/sit...wledge-and-win)
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  • Remove duplicate in RNAseq

    I would like to get opinion about remove duplicate of aligned reads on a reference genome before estimate transcriptional abundances.

    What do you think we should do or not ? And why ?

    There are some Thread that related with this issue, however it would be nice to get more opinion.

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