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        <dc:title>Identification and validation of insertion–deletion polymorphisms in pigeonpea</dc:title>
        <dc:creator>Singh, S K</dc:creator>
        <dc:creator>Kale, S M</dc:creator>
        <dc:creator>Saxena, R K</dc:creator>
        <dc:creator>Sinha, P</dc:creator>
        <dc:creator>Parupalli, S</dc:creator>
        <dc:creator>Suryanaraya, V</dc:creator>
        <dc:creator>Obala, J</dc:creator>
        <dc:creator>Sameer Kumar, C V</dc:creator>
        <dc:creator>Varshney, R K</dc:creator>
        <dc:subject>Pigeonpea</dc:subject>
        <dc:subject>Genetics and Genomics</dc:subject>
        <dc:description>Completely sequenced plant genomes provide scope for designing&#13;
a large number of genome wide insertion–deletion (InDel)&#13;
markers, which are useful in various aspects of crop breeding and&#13;
genetic analysis. With the objective of developing InDel markers&#13;
from pigeonpea genome, the re-sequencing data of eight MAGIC&#13;
parental lines were used to identify InDels using Dindel software.&#13;
As a result, a total of 102,181 InDels were identified. Of these&#13;
70158 InDels were found unique. The higher number of InDels&#13;
were found in intergenic (43%) followed by upstream (26%)&#13;
and downstream (24%) regions. A total of 6.93 % of Indels were&#13;
found in the genic region. Out of 70158 InDels, 2,426 (1032 Insertions&#13;
and 1394 deletions) with ≥20 bp size among different&#13;
parental lines were selected. Average distribution of selected&#13;
2426 InDels was found 220 InDels/LG with maximum number&#13;
of InDels on CcLG11 (385 InDels) and minimum number of In-&#13;
Dels on CcLG05 (70 InDels). A set of 293 InDels could assess&#13;
genetic diversity and establish phylogenetic relationships among&#13;
16 parental lines of different mapping populations. Validation of&#13;
these primer pairs on parental lines of different mapping population&#13;
resulted in higher amplification success rate (≥83%) with&#13;
almost 52.04% polymorphism rate among parental lines on 3%&#13;
agarose gel. The number of alleles per locus ranged from 2 to&#13;
9 with an average of 3.8 alleles. Further, to track the genome&#13;
of parents in complex funnel crossing scheme of pigeonpea&#13;
MAGIC population at 28-two way, 14-four way and 7-eigth way&#13;
stages, we have identified unique InDel primers for each of the&#13;
8 MAGIC parents. The result showed that InDel markers with&#13;
their high polymorphic potential in comparison to SSR markers&#13;
would be preferred candidate markers in various marker-based&#13;
applications in pigeonpea genetics and breeding.</dc:description>
        <dc:date>2017-02</dc:date>
        <dc:type>Conference or Workshop Item</dc:type>
        <dc:type>PeerReviewed</dc:type>
        <dc:format>application/pdf</dc:format>
        <dc:language>en</dc:language>
        <dc:identifier>http://oar.icrisat.org/10315/1/Abstract_Book_423.pdf</dc:identifier>
        <dc:identifier>  Singh, S K and Kale, S M and Saxena, R K and Sinha, P and Parupalli, S and Suryanaraya, V and Obala, J and Sameer Kumar, C V and Varshney, R K  (2017) Identification and validation of insertion–deletion polymorphisms in pigeonpea.  In: InterDrought-V, February 21-25, 2017, Hyderabad, India.     </dc:identifier></oai_dc:dc>
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