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<div><span></span>Dear sir:</div><div> After assemblying, I got many contigs and their order in each chromosome.</div><div> What I have done is merging these contigs into each chromosomes followed by the order, with 100 Ns inserted betwwen each contigs. So that I got chr1 chr2......Then I ran the repeatmodeler, predictor to annotate it.</div><div><br></div><div> Could my way reach a high-quality result? Should I use all the contigs to mask repeats and practice predictor?</div><div> Is there any better way to do genome-wide annotation?</div><div><br></div><div> I'm looking forward to your reply!</div><div> Best wishes!</div><div> </div>
<div>Chao Chao</div><hr style="width: 210px; height: 1px;" color="#b5c4df" size="1" align="left">
<div><span><div style="MARGIN: 10px; FONT-FAMILY: verdana; FONT-SIZE: 10pt">2017.02.28</div></span></div>
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