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Hi,
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<div class="">Do you have data that can precisely place each of your contigs in their position on the chromosome? Without that, this isn’t even possible, since a gff3 file with the chromosomes instead of the contigs requires each contig’s position in the chromosome. </div>
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<div class="">And in any case, I don’t think there is a script in the maker tools that does what you’re asking. Maybe someone else has made a script to do that. </div>
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<div class="">~Daniel</div>
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<div class="">On Mar 6, 2017, at 7:24 AM, <a href="mailto:dcg@cau.edu.cn" class="">
dcg@cau.edu.cn</a> wrote:</div>
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<span class=""></span>Dear sir:</div>
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Hello, I am doing my utmost to sdudy on annotation now.</div>
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However, I have been confused on results handlng recently. After alignment, practice and curation, we can get good gene model and merge them by<span class="Apple-converted-space"> </span><b class="">gff_merge</b><span class="Apple-converted-space"> </span>and<span class="Apple-converted-space"> </span><b class="">fasta_merge.
But how can I merge them into different chromosomes like Homo_sapiens.GRCh38.87.chromosome.11.gff3.gz?<span class="Apple-converted-space"> </span></b>I don't just want results of different contigs.</div>
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I'm looking forward to your reply. Thanks a lot!</div>
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Best wishes!</div>
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Chao Chao</div>
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<div class="">2017.03.06</div>
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