Visualizes introgressions at nucleotide or SNP (Single Nucleotide Polymorphisms) accuracy. The software selects homozygous SNPs from Variant Call Format (VCF) and filters out heterozygous SNPs, multi-nucleotide polymorphisms and insertion-deletions.
Biology, Agricultural science, Genetics
Aflitos SA, Sanchez-Perez G, de Ridder D, Fransz P, Schranz ME, de Jong H, Peters SA "Introgression browser: high-throughput whole-genome SNP visualization." Plant J. 2015; 82(1):174-82 https://doi.org/10.1111/tpj.12800
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