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Select reference genome
Choose a Reference Genome
Select type of your reads
Illumina Single end reads
Illumina Paired end reads
454 Single end reads
454 Paired end reads
Ion Torrent Single end reads
Assembled Genomes
SNPs files (vcf)
Select minimum coverage
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Select minimum distance between SNPs (prune)
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Select minimum distance to end of sequence (option for assemble genomes)
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Compared to Genome Database
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Select the genomes to compare with
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List of Selected genomes to compare with