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        <dc:title>A sorghum practical haplotype graph facilitates genome‐wide imputation and cost‐effective genomic prediction</dc:title>
        <dc:creator>Jensen, S E</dc:creator>
        <dc:creator>Charles, J R</dc:creator>
        <dc:creator>Muleta, K</dc:creator>
        <dc:creator>Bradbury, P J</dc:creator>
        <dc:creator>Casstevens, T</dc:creator>
        <dc:creator>Deshpande, S P</dc:creator>
        <dc:creator>Gore, M A</dc:creator>
        <dc:creator>Gupta, R</dc:creator>
        <dc:creator>Ilut, D C</dc:creator>
        <dc:creator>Johnson, L</dc:creator>
        <dc:creator>Lozano, R</dc:creator>
        <dc:creator>Miller, Z</dc:creator>
        <dc:creator>Ramu, P</dc:creator>
        <dc:creator>Rathore, A</dc:creator>
        <dc:creator>Romay, M C</dc:creator>
        <dc:creator>Upadhyaya, H D</dc:creator>
        <dc:creator>Varshney, R K</dc:creator>
        <dc:creator>Morris, G P</dc:creator>
        <dc:creator>Pressoir, G</dc:creator>
        <dc:creator>Buckler, E S</dc:creator>
        <dc:creator>Ramstein, G P</dc:creator>
        <dc:subject>Plant Breeding</dc:subject>
        <dc:subject>Sorghum</dc:subject>
        <dc:subject>Genetics and Genomics</dc:subject>
        <dc:description>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.</dc:description>
        <dc:publisher>Crop Science Society of America</dc:publisher>
        <dc:date>2020-03</dc:date>
        <dc:type>Article</dc:type>
        <dc:type>PeerReviewed</dc:type>
        <dc:format>application/pdf</dc:format>
        <dc:language>en</dc:language>
        <dc:identifier>http://oar.icrisat.org/11584/1/tpg2.20009.pdf</dc:identifier>
        <dc:identifier>  Jensen, S E and Charles, J R and Muleta, K and Bradbury, P J and Casstevens, T and Deshpande, S P and Gore, M A and Gupta, R and Ilut, D C and Johnson, L and Lozano, R and Miller, Z and Ramu, P and Rathore, A and Romay, M C and Upadhyaya, H D and Varshney, R K and Morris, G P and Pressoir, G and Buckler, E S and Ramstein, G P  (2020) A sorghum practical haplotype graph facilitates genome‐wide imputation and cost‐effective genomic prediction.  The Plant Genome (TSI), 13 (1).  pp. 1-15.  ISSN 1940-3372     </dc:identifier>
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