2009
DOI: 10.1007/s11032-009-9271-1
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Construction of a comprehensive PCR-based marker linkage map and QTL mapping for fiber quality traits in upland cotton (Gossypium hirsutum L.)

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Cited by 136 publications
(132 citation statements)
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“…A total of 16405 SSR primer pairs were used to screen for polymorphic markers between P 1 and P 2 . Among these primers, 13468 pairs of primers included types of BNL, NAU, TM, JESPER, CIR, HAU, CM, MUSS, MUSB, and MUCS, which were previously described in detail [8][9][10]14,21,22]; information on these primers can be obtained from the Cotton Microsatellite Database (http://www.cottonmarker.org). The remaining 2937 primer pairs were designed and developed from the DNA sequence library [23].…”
Section: Dna Extraction and Genotype Analysismentioning
confidence: 99%
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“…A total of 16405 SSR primer pairs were used to screen for polymorphic markers between P 1 and P 2 . Among these primers, 13468 pairs of primers included types of BNL, NAU, TM, JESPER, CIR, HAU, CM, MUSS, MUSB, and MUCS, which were previously described in detail [8][9][10]14,21,22]; information on these primers can be obtained from the Cotton Microsatellite Database (http://www.cottonmarker.org). The remaining 2937 primer pairs were designed and developed from the DNA sequence library [23].…”
Section: Dna Extraction and Genotype Analysismentioning
confidence: 99%
“…The assignment of linkage groups to chromosomes was based on backbone linkage maps [4,8,9,13,14,26]. When no chromosome inference was available, the linkage group was described as un××, where ×× refers to its serial number.…”
Section: Map Construction and Qtl Analysismentioning
confidence: 99%
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