<mods:mods version="3.3" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-3.xsd" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"><mods:titleInfo><mods:title>A sorghum practical haplotype graph facilitates genome‐wide imputation and cost‐effective genomic prediction</mods:title></mods:titleInfo><mods:name type="personal"><mods:namePart type="given">S E</mods:namePart><mods:namePart type="family">Jensen</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">J R</mods:namePart><mods:namePart type="family">Charles</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">K</mods:namePart><mods:namePart type="family">Muleta</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">P J</mods:namePart><mods:namePart type="family">Bradbury</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">T</mods:namePart><mods:namePart type="family">Casstevens</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">S P</mods:namePart><mods:namePart type="family">Deshpande</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">M A</mods:namePart><mods:namePart type="family">Gore</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">R</mods:namePart><mods:namePart type="family">Gupta</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">D C</mods:namePart><mods:namePart type="family">Ilut</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">L</mods:namePart><mods:namePart type="family">Johnson</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">R</mods:namePart><mods:namePart type="family">Lozano</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">Z</mods:namePart><mods:namePart type="family">Miller</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">P</mods:namePart><mods:namePart type="family">Ramu</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">A</mods:namePart><mods:namePart type="family">Rathore</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">M C</mods:namePart><mods:namePart type="family">Romay</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">H D</mods:namePart><mods:namePart type="family">Upadhyaya</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">R K</mods:namePart><mods:namePart type="family">Varshney</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">G P</mods:namePart><mods:namePart type="family">Morris</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">G</mods:namePart><mods:namePart type="family">Pressoir</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">E S</mods:namePart><mods:namePart type="family">Buckler</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">G P</mods:namePart><mods:namePart type="family">Ramstein</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:abstract>Successful management and utilization of increasingly large genomic datasets is&#13;
essential for breeding programs to accelerate cultivar development. To help with&#13;
this, we developed a Sorghum bicolor Practical Haplotype Graph (PHG) pangenome&#13;
database that stores haplotypes and variant information. We developed two PHGs&#13;
in sorghum that were used to identify genome-wide variants for 24 founders of the&#13;
Chibas sorghum breeding program from 0.01x sequence coverage. The PHG called&#13;
single nucleotide polymorphisms (SNPs) with 5.9% error at 0.01x coverage—only&#13;
3% higher than PHG error when calling SNPs from 8x coverage sequence. Additionally,&#13;
207 progenies from the Chibas genomic selection (GS) training population&#13;
were sequenced and processed through the PHG. Missing genotypes were imputed&#13;
from PHG parental haplotypes and used for genomic prediction. Mean prediction&#13;
accuracies with PHG SNP calls range from .57–.73 and are similar to prediction&#13;
accuracies obtained with genotyping-by-sequencing or targeted amplicon sequencing&#13;
(rhAmpSeq) markers. This study demonstrates the use of a sorghum PHG to impute SNPs from low-coverage sequence data and shows that the PHG can unify&#13;
genotype calls across multiple sequencing platforms. By reducing input sequence&#13;
requirements, the PHG can decrease the cost of genotyping, make GS more feasible,&#13;
and facilitate larger breeding populations. Our results demonstrate that the PHG is a&#13;
useful research and breeding tool that maintains variant information from a diverse&#13;
group of taxa, stores sequence data in a condensed but readily accessible format, unifies&#13;
genotypes across genotyping platforms, and provides a cost-effective option for&#13;
genomic selection.</mods:abstract><mods:classification authority="lcc">Plant Breeding</mods:classification><mods:classification authority="lcc">Sorghum</mods:classification><mods:classification authority="lcc">Genetics and Genomics</mods:classification><mods:originInfo><mods:dateIssued encoding="iso8061">2020-03</mods:dateIssued></mods:originInfo><mods:originInfo><mods:publisher>Crop Science Society of America</mods:publisher></mods:originInfo><mods:genre>Article</mods:genre></mods:mods>