Review and Analysis of Limitations in Ways to Improve Conventional Potato Breeding
Abstract A number of improvements to conventional potato breeding are possible but they all have their limitations which need to be appreciated in designing new breeding programmes. Selection for quantitative traits between crosses before selection within the most promising ones can solve the proble...
Ausführliche Beschreibung
Autor*in: |
Bradshaw, John E. [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2017 |
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Schlagwörter: |
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Anmerkung: |
© European Association for Potato Research 2017 |
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Übergeordnetes Werk: |
Enthalten in: Potato research - Dordrecht [u.a.] : Springer, 1958, 60(2017), 2 vom: Juni, Seite 171-193 |
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Übergeordnetes Werk: |
volume:60 ; year:2017 ; number:2 ; month:06 ; pages:171-193 |
Links: |
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DOI / URN: |
10.1007/s11540-017-9346-z |
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Katalog-ID: |
SPR020644205 |
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520 | |a Abstract A number of improvements to conventional potato breeding are possible but they all have their limitations which need to be appreciated in designing new breeding programmes. Selection for quantitative traits between crosses before selection within the most promising ones can solve the problem of the inability of intense early-generation selection to affect most economically important traits. It also allows full-sib family selection to be practised but the rate of progress is limited by a low intensity of selection so that continued recurrent selection is required to accumulate small improvements into worthwhile ones. The rate of progress from combined between and within cross selection is limited by the number of vegetative generations required to complete all necessary phenotypic assessments, as well as by the intensities of selection. Both problems could be solved by genomic selection provided adequate selection accuracy can be achieved. However, lack of accurate large-scale phenotyping may limit the use of genomic selection in the immediate future. Marker-assisted selection can be used to stack major genes and QTL alleles of large effect in new cultivars, but the required population sizes will limit the number of unlinked genes going much beyond eight. Site-directed transformation should speed the stacking of transgenes in a new cultivar and hence increase the number of major improvements that can be made by genetic transformation. | ||
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10.1007/s11540-017-9346-z doi (DE-627)SPR020644205 (SPR)s11540-017-9346-z-e DE-627 ger DE-627 rakwb eng Bradshaw, John E. verfasserin aut Review and Analysis of Limitations in Ways to Improve Conventional Potato Breeding 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Association for Potato Research 2017 Abstract A number of improvements to conventional potato breeding are possible but they all have their limitations which need to be appreciated in designing new breeding programmes. Selection for quantitative traits between crosses before selection within the most promising ones can solve the problem of the inability of intense early-generation selection to affect most economically important traits. It also allows full-sib family selection to be practised but the rate of progress is limited by a low intensity of selection so that continued recurrent selection is required to accumulate small improvements into worthwhile ones. The rate of progress from combined between and within cross selection is limited by the number of vegetative generations required to complete all necessary phenotypic assessments, as well as by the intensities of selection. Both problems could be solved by genomic selection provided adequate selection accuracy can be achieved. However, lack of accurate large-scale phenotyping may limit the use of genomic selection in the immediate future. Marker-assisted selection can be used to stack major genes and QTL alleles of large effect in new cultivars, but the required population sizes will limit the number of unlinked genes going much beyond eight. Site-directed transformation should speed the stacking of transgenes in a new cultivar and hence increase the number of major improvements that can be made by genetic transformation. Between cross selection (dpeaa)DE-He213 Clonal selection (dpeaa)DE-He213 Family selection (dpeaa)DE-He213 Genetic transformation (dpeaa)DE-He213 Genomic selection (dpeaa)DE-He213 Marker-assisted selection (dpeaa)DE-He213 Enthalten in Potato research Dordrecht [u.a.] : Springer, 1958 60(2017), 2 vom: Juni, Seite 171-193 (DE-627)512299366 (DE-600)2235908-4 1871-4528 nnns volume:60 year:2017 number:2 month:06 pages:171-193 https://dx.doi.org/10.1007/s11540-017-9346-z lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 60 2017 2 06 171-193 |
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10.1007/s11540-017-9346-z doi (DE-627)SPR020644205 (SPR)s11540-017-9346-z-e DE-627 ger DE-627 rakwb eng Bradshaw, John E. verfasserin aut Review and Analysis of Limitations in Ways to Improve Conventional Potato Breeding 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Association for Potato Research 2017 Abstract A number of improvements to conventional potato breeding are possible but they all have their limitations which need to be appreciated in designing new breeding programmes. Selection for quantitative traits between crosses before selection within the most promising ones can solve the problem of the inability of intense early-generation selection to affect most economically important traits. It also allows full-sib family selection to be practised but the rate of progress is limited by a low intensity of selection so that continued recurrent selection is required to accumulate small improvements into worthwhile ones. The rate of progress from combined between and within cross selection is limited by the number of vegetative generations required to complete all necessary phenotypic assessments, as well as by the intensities of selection. Both problems could be solved by genomic selection provided adequate selection accuracy can be achieved. However, lack of accurate large-scale phenotyping may limit the use of genomic selection in the immediate future. Marker-assisted selection can be used to stack major genes and QTL alleles of large effect in new cultivars, but the required population sizes will limit the number of unlinked genes going much beyond eight. Site-directed transformation should speed the stacking of transgenes in a new cultivar and hence increase the number of major improvements that can be made by genetic transformation. Between cross selection (dpeaa)DE-He213 Clonal selection (dpeaa)DE-He213 Family selection (dpeaa)DE-He213 Genetic transformation (dpeaa)DE-He213 Genomic selection (dpeaa)DE-He213 Marker-assisted selection (dpeaa)DE-He213 Enthalten in Potato research Dordrecht [u.a.] : Springer, 1958 60(2017), 2 vom: Juni, Seite 171-193 (DE-627)512299366 (DE-600)2235908-4 1871-4528 nnns volume:60 year:2017 number:2 month:06 pages:171-193 https://dx.doi.org/10.1007/s11540-017-9346-z lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 60 2017 2 06 171-193 |
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10.1007/s11540-017-9346-z doi (DE-627)SPR020644205 (SPR)s11540-017-9346-z-e DE-627 ger DE-627 rakwb eng Bradshaw, John E. verfasserin aut Review and Analysis of Limitations in Ways to Improve Conventional Potato Breeding 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Association for Potato Research 2017 Abstract A number of improvements to conventional potato breeding are possible but they all have their limitations which need to be appreciated in designing new breeding programmes. Selection for quantitative traits between crosses before selection within the most promising ones can solve the problem of the inability of intense early-generation selection to affect most economically important traits. It also allows full-sib family selection to be practised but the rate of progress is limited by a low intensity of selection so that continued recurrent selection is required to accumulate small improvements into worthwhile ones. The rate of progress from combined between and within cross selection is limited by the number of vegetative generations required to complete all necessary phenotypic assessments, as well as by the intensities of selection. Both problems could be solved by genomic selection provided adequate selection accuracy can be achieved. However, lack of accurate large-scale phenotyping may limit the use of genomic selection in the immediate future. Marker-assisted selection can be used to stack major genes and QTL alleles of large effect in new cultivars, but the required population sizes will limit the number of unlinked genes going much beyond eight. Site-directed transformation should speed the stacking of transgenes in a new cultivar and hence increase the number of major improvements that can be made by genetic transformation. Between cross selection (dpeaa)DE-He213 Clonal selection (dpeaa)DE-He213 Family selection (dpeaa)DE-He213 Genetic transformation (dpeaa)DE-He213 Genomic selection (dpeaa)DE-He213 Marker-assisted selection (dpeaa)DE-He213 Enthalten in Potato research Dordrecht [u.a.] : Springer, 1958 60(2017), 2 vom: Juni, Seite 171-193 (DE-627)512299366 (DE-600)2235908-4 1871-4528 nnns volume:60 year:2017 number:2 month:06 pages:171-193 https://dx.doi.org/10.1007/s11540-017-9346-z lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 60 2017 2 06 171-193 |
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10.1007/s11540-017-9346-z doi (DE-627)SPR020644205 (SPR)s11540-017-9346-z-e DE-627 ger DE-627 rakwb eng Bradshaw, John E. verfasserin aut Review and Analysis of Limitations in Ways to Improve Conventional Potato Breeding 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Association for Potato Research 2017 Abstract A number of improvements to conventional potato breeding are possible but they all have their limitations which need to be appreciated in designing new breeding programmes. Selection for quantitative traits between crosses before selection within the most promising ones can solve the problem of the inability of intense early-generation selection to affect most economically important traits. It also allows full-sib family selection to be practised but the rate of progress is limited by a low intensity of selection so that continued recurrent selection is required to accumulate small improvements into worthwhile ones. The rate of progress from combined between and within cross selection is limited by the number of vegetative generations required to complete all necessary phenotypic assessments, as well as by the intensities of selection. Both problems could be solved by genomic selection provided adequate selection accuracy can be achieved. However, lack of accurate large-scale phenotyping may limit the use of genomic selection in the immediate future. Marker-assisted selection can be used to stack major genes and QTL alleles of large effect in new cultivars, but the required population sizes will limit the number of unlinked genes going much beyond eight. Site-directed transformation should speed the stacking of transgenes in a new cultivar and hence increase the number of major improvements that can be made by genetic transformation. Between cross selection (dpeaa)DE-He213 Clonal selection (dpeaa)DE-He213 Family selection (dpeaa)DE-He213 Genetic transformation (dpeaa)DE-He213 Genomic selection (dpeaa)DE-He213 Marker-assisted selection (dpeaa)DE-He213 Enthalten in Potato research Dordrecht [u.a.] : Springer, 1958 60(2017), 2 vom: Juni, Seite 171-193 (DE-627)512299366 (DE-600)2235908-4 1871-4528 nnns volume:60 year:2017 number:2 month:06 pages:171-193 https://dx.doi.org/10.1007/s11540-017-9346-z lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 60 2017 2 06 171-193 |
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10.1007/s11540-017-9346-z doi (DE-627)SPR020644205 (SPR)s11540-017-9346-z-e DE-627 ger DE-627 rakwb eng Bradshaw, John E. verfasserin aut Review and Analysis of Limitations in Ways to Improve Conventional Potato Breeding 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Association for Potato Research 2017 Abstract A number of improvements to conventional potato breeding are possible but they all have their limitations which need to be appreciated in designing new breeding programmes. Selection for quantitative traits between crosses before selection within the most promising ones can solve the problem of the inability of intense early-generation selection to affect most economically important traits. It also allows full-sib family selection to be practised but the rate of progress is limited by a low intensity of selection so that continued recurrent selection is required to accumulate small improvements into worthwhile ones. The rate of progress from combined between and within cross selection is limited by the number of vegetative generations required to complete all necessary phenotypic assessments, as well as by the intensities of selection. Both problems could be solved by genomic selection provided adequate selection accuracy can be achieved. However, lack of accurate large-scale phenotyping may limit the use of genomic selection in the immediate future. Marker-assisted selection can be used to stack major genes and QTL alleles of large effect in new cultivars, but the required population sizes will limit the number of unlinked genes going much beyond eight. Site-directed transformation should speed the stacking of transgenes in a new cultivar and hence increase the number of major improvements that can be made by genetic transformation. Between cross selection (dpeaa)DE-He213 Clonal selection (dpeaa)DE-He213 Family selection (dpeaa)DE-He213 Genetic transformation (dpeaa)DE-He213 Genomic selection (dpeaa)DE-He213 Marker-assisted selection (dpeaa)DE-He213 Enthalten in Potato research Dordrecht [u.a.] : Springer, 1958 60(2017), 2 vom: Juni, Seite 171-193 (DE-627)512299366 (DE-600)2235908-4 1871-4528 nnns volume:60 year:2017 number:2 month:06 pages:171-193 https://dx.doi.org/10.1007/s11540-017-9346-z lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 60 2017 2 06 171-193 |
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Enthalten in Potato research 60(2017), 2 vom: Juni, Seite 171-193 volume:60 year:2017 number:2 month:06 pages:171-193 |
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Enthalten in Potato research 60(2017), 2 vom: Juni, Seite 171-193 volume:60 year:2017 number:2 month:06 pages:171-193 |
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Bradshaw, John E. @@aut@@ |
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Bradshaw, John E. misc Between cross selection misc Clonal selection misc Family selection misc Genetic transformation misc Genomic selection misc Marker-assisted selection Review and Analysis of Limitations in Ways to Improve Conventional Potato Breeding |
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Review and Analysis of Limitations in Ways to Improve Conventional Potato Breeding Between cross selection (dpeaa)DE-He213 Clonal selection (dpeaa)DE-He213 Family selection (dpeaa)DE-He213 Genetic transformation (dpeaa)DE-He213 Genomic selection (dpeaa)DE-He213 Marker-assisted selection (dpeaa)DE-He213 |
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Review and Analysis of Limitations in Ways to Improve Conventional Potato Breeding |
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review and analysis of limitations in ways to improve conventional potato breeding |
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Review and Analysis of Limitations in Ways to Improve Conventional Potato Breeding |
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Abstract A number of improvements to conventional potato breeding are possible but they all have their limitations which need to be appreciated in designing new breeding programmes. Selection for quantitative traits between crosses before selection within the most promising ones can solve the problem of the inability of intense early-generation selection to affect most economically important traits. It also allows full-sib family selection to be practised but the rate of progress is limited by a low intensity of selection so that continued recurrent selection is required to accumulate small improvements into worthwhile ones. The rate of progress from combined between and within cross selection is limited by the number of vegetative generations required to complete all necessary phenotypic assessments, as well as by the intensities of selection. Both problems could be solved by genomic selection provided adequate selection accuracy can be achieved. However, lack of accurate large-scale phenotyping may limit the use of genomic selection in the immediate future. Marker-assisted selection can be used to stack major genes and QTL alleles of large effect in new cultivars, but the required population sizes will limit the number of unlinked genes going much beyond eight. Site-directed transformation should speed the stacking of transgenes in a new cultivar and hence increase the number of major improvements that can be made by genetic transformation. © European Association for Potato Research 2017 |
abstractGer |
Abstract A number of improvements to conventional potato breeding are possible but they all have their limitations which need to be appreciated in designing new breeding programmes. Selection for quantitative traits between crosses before selection within the most promising ones can solve the problem of the inability of intense early-generation selection to affect most economically important traits. It also allows full-sib family selection to be practised but the rate of progress is limited by a low intensity of selection so that continued recurrent selection is required to accumulate small improvements into worthwhile ones. The rate of progress from combined between and within cross selection is limited by the number of vegetative generations required to complete all necessary phenotypic assessments, as well as by the intensities of selection. Both problems could be solved by genomic selection provided adequate selection accuracy can be achieved. However, lack of accurate large-scale phenotyping may limit the use of genomic selection in the immediate future. Marker-assisted selection can be used to stack major genes and QTL alleles of large effect in new cultivars, but the required population sizes will limit the number of unlinked genes going much beyond eight. Site-directed transformation should speed the stacking of transgenes in a new cultivar and hence increase the number of major improvements that can be made by genetic transformation. © European Association for Potato Research 2017 |
abstract_unstemmed |
Abstract A number of improvements to conventional potato breeding are possible but they all have their limitations which need to be appreciated in designing new breeding programmes. Selection for quantitative traits between crosses before selection within the most promising ones can solve the problem of the inability of intense early-generation selection to affect most economically important traits. It also allows full-sib family selection to be practised but the rate of progress is limited by a low intensity of selection so that continued recurrent selection is required to accumulate small improvements into worthwhile ones. The rate of progress from combined between and within cross selection is limited by the number of vegetative generations required to complete all necessary phenotypic assessments, as well as by the intensities of selection. Both problems could be solved by genomic selection provided adequate selection accuracy can be achieved. However, lack of accurate large-scale phenotyping may limit the use of genomic selection in the immediate future. Marker-assisted selection can be used to stack major genes and QTL alleles of large effect in new cultivars, but the required population sizes will limit the number of unlinked genes going much beyond eight. Site-directed transformation should speed the stacking of transgenes in a new cultivar and hence increase the number of major improvements that can be made by genetic transformation. © European Association for Potato Research 2017 |
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Review and Analysis of Limitations in Ways to Improve Conventional Potato Breeding |
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Selection for quantitative traits between crosses before selection within the most promising ones can solve the problem of the inability of intense early-generation selection to affect most economically important traits. It also allows full-sib family selection to be practised but the rate of progress is limited by a low intensity of selection so that continued recurrent selection is required to accumulate small improvements into worthwhile ones. The rate of progress from combined between and within cross selection is limited by the number of vegetative generations required to complete all necessary phenotypic assessments, as well as by the intensities of selection. Both problems could be solved by genomic selection provided adequate selection accuracy can be achieved. However, lack of accurate large-scale phenotyping may limit the use of genomic selection in the immediate future. Marker-assisted selection can be used to stack major genes and QTL alleles of large effect in new cultivars, but the required population sizes will limit the number of unlinked genes going much beyond eight. 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