000 | 02955nab a22003857a 4500 | ||
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001 | G94896 | ||
003 | MX-TxCIM | ||
005 | 20220704150302.0 | ||
008 | 220704s2010 xxu|||p|op||| 00| 0 eng d | ||
022 | _a1940-3372 (Online) | ||
024 | 8 | _ahttps://doi.org/10.3835/plantgenome2010.06.0013 | |
040 | _aMX-TxCIM | ||
041 | _aeng | ||
090 | _aCIS-6280 | ||
100 | 1 |
_aCórdoba, J.M. _927966 |
|
245 | 1 | 0 | _aIdentification and mapping of simple sequence repeat markers from common bean (phaseolus vulgaris l.) bacterial artificial chromosome end sequences for genome characterization and genetic-physical map integration |
260 |
_aMadison, WI (USA) : _bCSSA : _bWiley, _c2010. |
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500 | _aPeer-review: Yes - Open Access: Yes|http://science.thomsonreuters.com/cgi-bin/jrnlst/jlresults.cgi?PC=MASTER&ISSN=1940-3372 | ||
500 | _aPeer review | ||
500 | _aOpen Access | ||
520 | _aMicrosatellite markers or simple sequence repeat (SSR) loci are useful for diversity characterization and genetic?physical mapping. Different in silico microsatellite search methods have been developed for mining bacterial artificial chromosome (BAC) end sequences for SSRs. The overall goal of this study was genome characterization based on SSRs in 89,017 BAC end sequences (BESs) from the G19833 common bean (Phaseolus vulgaris L.) library. Another objective was to identify new SSR taking into account three tandem motif identification programs (Automated Microsatellite Marker Development [AMMD], Tandem Repeats Finder [TRF], and SSRLocator [SSRL]). Among the microsatellite search engines, SSRL identified the highest number of SSRs; however, when primer design was attempted, the number dropped due to poor primer design regions. Automated Microsatellite Marker Development software identified many SSRs with valuable AT/TA or AG/TC motifs, while TRF found fewer SSRs and produced no primers. A subgroup of 323 AT-rich, di-, and trinucleotide SSRs were selected from the AMMD results and used in a parental survey with DOR364 and G19833, of which 75 could be mapped in the corresponding population; these represented 4052 BAC clones. Together with 92 previously mapped BES- and 114 non-BES-derived markers, a total of 280 SSRs were included in the polymerase chain reaction (PCR)-based map, integrating a total of 8232 BAC clones in 162 contigs from the physical map. | ||
546 | _aText in English | ||
595 | _aCSC | ||
650 | 7 |
_99039 _aPhaseolus vulgaris _2AGROVOC |
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650 | 7 |
_91848 _aGenetic markers _2AGROVOC |
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650 | 7 |
_92261 _aMicrosatellites _2AGROVOC |
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650 | 7 |
_94190 _aGenetic maps _2AGROVOC |
|
700 | 1 |
_aChavarro, C. _927967 |
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700 | 1 |
_aRojas, F. _927968 |
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700 | 1 |
_aMuñoz, C. _927969 |
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700 | 1 |
_aBlair, M.W. _921809 |
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773 | 0 |
_tPlant Genome _gv. 3, no. 3, p. 154-165 _dMadison, WI (USA) : CSSA : Wiley, 2010. _wG94757 _x1940-3372 |
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856 | 4 |
_uhttp://hdl.handle.net/10883/1845 _yOpen Access through DSpace |
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942 |
_cJA _2ddc _n0 |
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999 |
_c28370 _d28370 |