A new set-valued system identification approach to identifying rare genetic variants for ordered categorical phenotype

Gespeichert in:

Autor*in:	Bi, Wenjian [verfasserIn] Kang, Guolian Cui, Yuehua Li, Yun Hartford, Christine M Leung, Wing Zhang, Ji-Feng

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2014

Schlagwörter:	Association Study Minor Allele Frequency Rare Variant Genetic Association Study Categorical Phenotype

Anmerkung:	© Bi et al; licensee BioMed Central Ltd. 2014. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (

Übergeordnetes Werk:	Enthalten in: BMC bioinformatics - London : BioMed Central, 2000, 15(2014), Suppl 10 vom: 29. Sept.
Übergeordnetes Werk:	volume:15 ; year:2014 ; number:Suppl 10 ; day:29 ; month:09

Links:	Volltext

DOI / URN:	10.1186/1471-2105-15-S10-P29

Katalog-ID:	SPR026894289

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allfields	10.1186/1471-2105-15-S10-P29 doi (DE-627)SPR026894289 (SPR)1471-2105-15-S10-P29-e DE-627 ger DE-627 rakwb eng Bi, Wenjian verfasserin aut A new set-valued system identification approach to identifying rare genetic variants for ordered categorical phenotype 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Bi et al; licensee BioMed Central Ltd. 2014. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Association Study (dpeaa)DE-He213 Minor Allele Frequency (dpeaa)DE-He213 Rare Variant (dpeaa)DE-He213 Genetic Association Study (dpeaa)DE-He213 Categorical Phenotype (dpeaa)DE-He213 Kang, Guolian aut Cui, Yuehua aut Li, Yun aut Hartford, Christine M aut Leung, Wing aut Zhang, Ji-Feng aut Enthalten in BMC bioinformatics London : BioMed Central, 2000 15(2014), Suppl 10 vom: 29. Sept. (DE-627)326644814 (DE-600)2041484-5 1471-2105 nnns volume:15 year:2014 number:Suppl 10 day:29 month:09 https://dx.doi.org/10.1186/1471-2105-15-S10-P29 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 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_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 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_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 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_4335 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 15 2014 Suppl 10 29 09
spelling	10.1186/1471-2105-15-S10-P29 doi (DE-627)SPR026894289 (SPR)1471-2105-15-S10-P29-e DE-627 ger DE-627 rakwb eng Bi, Wenjian verfasserin aut A new set-valued system identification approach to identifying rare genetic variants for ordered categorical phenotype 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Bi et al; licensee BioMed Central Ltd. 2014. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Association Study (dpeaa)DE-He213 Minor Allele Frequency (dpeaa)DE-He213 Rare Variant (dpeaa)DE-He213 Genetic Association Study (dpeaa)DE-He213 Categorical Phenotype (dpeaa)DE-He213 Kang, Guolian aut Cui, Yuehua aut Li, Yun aut Hartford, Christine M aut Leung, Wing aut Zhang, Ji-Feng aut Enthalten in BMC bioinformatics London : BioMed Central, 2000 15(2014), Suppl 10 vom: 29. Sept. (DE-627)326644814 (DE-600)2041484-5 1471-2105 nnns volume:15 year:2014 number:Suppl 10 day:29 month:09 https://dx.doi.org/10.1186/1471-2105-15-S10-P29 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 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_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 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_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 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_4335 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 15 2014 Suppl 10 29 09
allfields_unstemmed	10.1186/1471-2105-15-S10-P29 doi (DE-627)SPR026894289 (SPR)1471-2105-15-S10-P29-e DE-627 ger DE-627 rakwb eng Bi, Wenjian verfasserin aut A new set-valued system identification approach to identifying rare genetic variants for ordered categorical phenotype 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Bi et al; licensee BioMed Central Ltd. 2014. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Association Study (dpeaa)DE-He213 Minor Allele Frequency (dpeaa)DE-He213 Rare Variant (dpeaa)DE-He213 Genetic Association Study (dpeaa)DE-He213 Categorical Phenotype (dpeaa)DE-He213 Kang, Guolian aut Cui, Yuehua aut Li, Yun aut Hartford, Christine M aut Leung, Wing aut Zhang, Ji-Feng aut Enthalten in BMC bioinformatics London : BioMed Central, 2000 15(2014), Suppl 10 vom: 29. Sept. (DE-627)326644814 (DE-600)2041484-5 1471-2105 nnns volume:15 year:2014 number:Suppl 10 day:29 month:09 https://dx.doi.org/10.1186/1471-2105-15-S10-P29 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 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_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 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_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 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_4335 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 15 2014 Suppl 10 29 09
allfieldsGer	10.1186/1471-2105-15-S10-P29 doi (DE-627)SPR026894289 (SPR)1471-2105-15-S10-P29-e DE-627 ger DE-627 rakwb eng Bi, Wenjian verfasserin aut A new set-valued system identification approach to identifying rare genetic variants for ordered categorical phenotype 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Bi et al; licensee BioMed Central Ltd. 2014. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Association Study (dpeaa)DE-He213 Minor Allele Frequency (dpeaa)DE-He213 Rare Variant (dpeaa)DE-He213 Genetic Association Study (dpeaa)DE-He213 Categorical Phenotype (dpeaa)DE-He213 Kang, Guolian aut Cui, Yuehua aut Li, Yun aut Hartford, Christine M aut Leung, Wing aut Zhang, Ji-Feng aut Enthalten in BMC bioinformatics London : BioMed Central, 2000 15(2014), Suppl 10 vom: 29. Sept. (DE-627)326644814 (DE-600)2041484-5 1471-2105 nnns volume:15 year:2014 number:Suppl 10 day:29 month:09 https://dx.doi.org/10.1186/1471-2105-15-S10-P29 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 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_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 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_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 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_4335 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 15 2014 Suppl 10 29 09
allfieldsSound	10.1186/1471-2105-15-S10-P29 doi (DE-627)SPR026894289 (SPR)1471-2105-15-S10-P29-e DE-627 ger DE-627 rakwb eng Bi, Wenjian verfasserin aut A new set-valued system identification approach to identifying rare genetic variants for ordered categorical phenotype 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Bi et al; licensee BioMed Central Ltd. 2014. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Association Study (dpeaa)DE-He213 Minor Allele Frequency (dpeaa)DE-He213 Rare Variant (dpeaa)DE-He213 Genetic Association Study (dpeaa)DE-He213 Categorical Phenotype (dpeaa)DE-He213 Kang, Guolian aut Cui, Yuehua aut Li, Yun aut Hartford, Christine M aut Leung, Wing aut Zhang, Ji-Feng aut Enthalten in BMC bioinformatics London : BioMed Central, 2000 15(2014), Suppl 10 vom: 29. Sept. (DE-627)326644814 (DE-600)2041484-5 1471-2105 nnns volume:15 year:2014 number:Suppl 10 day:29 month:09 https://dx.doi.org/10.1186/1471-2105-15-S10-P29 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 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_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 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_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 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_4335 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 15 2014 Suppl 10 29 09
language	English
source	Enthalten in BMC bioinformatics 15(2014), Suppl 10 vom: 29. Sept. volume:15 year:2014 number:Suppl 10 day:29 month:09
sourceStr	Enthalten in BMC bioinformatics 15(2014), Suppl 10 vom: 29. Sept. volume:15 year:2014 number:Suppl 10 day:29 month:09
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institution	findex.gbv.de
topic_facet	Association Study Minor Allele Frequency Rare Variant Genetic Association Study Categorical Phenotype
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container_title	BMC bioinformatics
authorswithroles_txt_mv	Bi, Wenjian @@aut@@ Kang, Guolian @@aut@@ Cui, Yuehua @@aut@@ Li, Yun @@aut@@ Hartford, Christine M @@aut@@ Leung, Wing @@aut@@ Zhang, Ji-Feng @@aut@@
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author	Bi, Wenjian
spellingShingle	Bi, Wenjian misc Association Study misc Minor Allele Frequency misc Rare Variant misc Genetic Association Study misc Categorical Phenotype A new set-valued system identification approach to identifying rare genetic variants for ordered categorical phenotype
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topic_title	A new set-valued system identification approach to identifying rare genetic variants for ordered categorical phenotype Association Study (dpeaa)DE-He213 Minor Allele Frequency (dpeaa)DE-He213 Rare Variant (dpeaa)DE-He213 Genetic Association Study (dpeaa)DE-He213 Categorical Phenotype (dpeaa)DE-He213
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title	A new set-valued system identification approach to identifying rare genetic variants for ordered categorical phenotype
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title_full	A new set-valued system identification approach to identifying rare genetic variants for ordered categorical phenotype
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title_sort	new set-valued system identification approach to identifying rare genetic variants for ordered categorical phenotype
title_auth	A new set-valued system identification approach to identifying rare genetic variants for ordered categorical phenotype
abstract	© Bi et al; licensee BioMed Central Ltd. 2014. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (
abstractGer	© Bi et al; licensee BioMed Central Ltd. 2014. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (
abstract_unstemmed	© Bi et al; licensee BioMed Central Ltd. 2014. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (
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title_short	A new set-valued system identification approach to identifying rare genetic variants for ordered categorical phenotype
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up_date	2024-07-03T23:19:02.642Z
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A new set-valued system identification approach to identifying rare genetic variants for ordered categorical phenotype

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