Bridging the Gap between Vertebrate Cytogenetics and Genomics with Single-Chromosome Sequencing (ChromSeq).

Genes (Basel) · 2021 · PMC7835784 · PMID 33478118

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highly significantno p-value reported

It has been widely employed in plants for the chromosome assignment of assembled genomes, leading to highly significant results (e.g., [ 30 , 31 , 32 , 33 , 34 , 35 , 36 , 37 ]).

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