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You searched for subject:(ChIP Seq). Showing records 1 – 30 of 152 total matches.

[1] [2] [3] [4] [5] [6]

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University of Ottawa

1. Griffith, Alexander. Non Parametric Unsupervised Clustering of ChIP Enrichment Regions Provides Isolation Vectors for Differential Functional Analysis .

Degree: 2016, University of Ottawa

 Gene transcription rates are influenced by proteins, known as Transcription Factors (TFs), that interact with DNA. The locations of TFs on the genome directly influence… (more)

Subjects/Keywords: ChIP-Seq; ChIP; R; PCA

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APA (6th Edition):

Griffith, A. (2016). Non Parametric Unsupervised Clustering of ChIP Enrichment Regions Provides Isolation Vectors for Differential Functional Analysis . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/35084

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Griffith, Alexander. “Non Parametric Unsupervised Clustering of ChIP Enrichment Regions Provides Isolation Vectors for Differential Functional Analysis .” 2016. Thesis, University of Ottawa. Accessed May 22, 2019. http://hdl.handle.net/10393/35084.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Griffith, Alexander. “Non Parametric Unsupervised Clustering of ChIP Enrichment Regions Provides Isolation Vectors for Differential Functional Analysis .” 2016. Web. 22 May 2019.

Vancouver:

Griffith A. Non Parametric Unsupervised Clustering of ChIP Enrichment Regions Provides Isolation Vectors for Differential Functional Analysis . [Internet] [Thesis]. University of Ottawa; 2016. [cited 2019 May 22]. Available from: http://hdl.handle.net/10393/35084.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Griffith A. Non Parametric Unsupervised Clustering of ChIP Enrichment Regions Provides Isolation Vectors for Differential Functional Analysis . [Thesis]. University of Ottawa; 2016. Available from: http://hdl.handle.net/10393/35084

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Saskatchewan

2. Palmer, Melissa B. 1992-. Investigating the Role of CsgD in Salmonella Biofilm Formation and Virulence.

Degree: 2018, University of Saskatchewan

 When exposed to environmental stress, a pure culture of Salmonella enterica serovar Typhimurium (S. Typhimurium) differentiates into two specialized cell types with 34% differential gene… (more)

Subjects/Keywords: Salmonella biofilm; ChIP-seq

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APA (6th Edition):

Palmer, M. B. 1. (2018). Investigating the Role of CsgD in Salmonella Biofilm Formation and Virulence. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/11402

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Palmer, Melissa B 1992-. “Investigating the Role of CsgD in Salmonella Biofilm Formation and Virulence.” 2018. Thesis, University of Saskatchewan. Accessed May 22, 2019. http://hdl.handle.net/10388/11402.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Palmer, Melissa B 1992-. “Investigating the Role of CsgD in Salmonella Biofilm Formation and Virulence.” 2018. Web. 22 May 2019.

Vancouver:

Palmer MB1. Investigating the Role of CsgD in Salmonella Biofilm Formation and Virulence. [Internet] [Thesis]. University of Saskatchewan; 2018. [cited 2019 May 22]. Available from: http://hdl.handle.net/10388/11402.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Palmer MB1. Investigating the Role of CsgD in Salmonella Biofilm Formation and Virulence. [Thesis]. University of Saskatchewan; 2018. Available from: http://hdl.handle.net/10388/11402

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Université Montpellier II

3. Salipante, Florian. Mise au point de méthodologies statistiques appliquées à des données issues de la génomique : puces à ADN, ChIP-chip et ChIP-Seq. : Development of statistical methodologies applied to genomics data : microarray, ChIP-chip and ChIP-Seq.

Degree: Docteur es, Biologie Santé, 2011, Université Montpellier II

La recherche dans le domaine de la génomique génère de données colossales dont la dimension ne cesse de s'accroître avec la technologie. Pour traiter cette… (more)

Subjects/Keywords: ChIP-chip; ChIP-Seq; Puces à ADN; Pot; Algorithme Génétique; Génome; ChIP-chip; ChIP-Seq; Microarray; Pot; Genetic Algorithm; Genome

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APA (6th Edition):

Salipante, F. (2011). Mise au point de méthodologies statistiques appliquées à des données issues de la génomique : puces à ADN, ChIP-chip et ChIP-Seq. : Development of statistical methodologies applied to genomics data : microarray, ChIP-chip and ChIP-Seq. (Doctoral Dissertation). Université Montpellier II. Retrieved from http://www.theses.fr/2011MON20176

Chicago Manual of Style (16th Edition):

Salipante, Florian. “Mise au point de méthodologies statistiques appliquées à des données issues de la génomique : puces à ADN, ChIP-chip et ChIP-Seq. : Development of statistical methodologies applied to genomics data : microarray, ChIP-chip and ChIP-Seq.” 2011. Doctoral Dissertation, Université Montpellier II. Accessed May 22, 2019. http://www.theses.fr/2011MON20176.

MLA Handbook (7th Edition):

Salipante, Florian. “Mise au point de méthodologies statistiques appliquées à des données issues de la génomique : puces à ADN, ChIP-chip et ChIP-Seq. : Development of statistical methodologies applied to genomics data : microarray, ChIP-chip and ChIP-Seq.” 2011. Web. 22 May 2019.

Vancouver:

Salipante F. Mise au point de méthodologies statistiques appliquées à des données issues de la génomique : puces à ADN, ChIP-chip et ChIP-Seq. : Development of statistical methodologies applied to genomics data : microarray, ChIP-chip and ChIP-Seq. [Internet] [Doctoral dissertation]. Université Montpellier II; 2011. [cited 2019 May 22]. Available from: http://www.theses.fr/2011MON20176.

Council of Science Editors:

Salipante F. Mise au point de méthodologies statistiques appliquées à des données issues de la génomique : puces à ADN, ChIP-chip et ChIP-Seq. : Development of statistical methodologies applied to genomics data : microarray, ChIP-chip and ChIP-Seq. [Doctoral Dissertation]. Université Montpellier II; 2011. Available from: http://www.theses.fr/2011MON20176

4. Nhim, Sandra. Mécanismes de régulation épigénétique chez l'insecte holocentrique ravageur de culture Spodoptera frugiperd, Lépidoptera, Noctuidae : Epigenetic regulation mecanisms in holocentric pest crop Spdoptera frugiperda, Lepidoptera, Noctuidae.

Degree: Docteur es, Mécanismes des interactions parasitaires pathogènes et symbiotiques, 2018, Montpellier

 Chez les eucaryotes, l’ADN est empaqueté dans des complexes protéiques d’histones nommés nucléosomes qui assurent sa conformation. Cet arrangement est hétérogène à travers le génome… (more)

Subjects/Keywords: Epigénétique; Hétérochromatine; Bioinformatique; ChIP-Seq; Mnase-Seq; Histones; Epigenetics; Heterochromatin; Bioinformatics; ChIP-Seq; Mnase-Seq; Histones

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APA (6th Edition):

Nhim, S. (2018). Mécanismes de régulation épigénétique chez l'insecte holocentrique ravageur de culture Spodoptera frugiperd, Lépidoptera, Noctuidae : Epigenetic regulation mecanisms in holocentric pest crop Spdoptera frugiperda, Lepidoptera, Noctuidae. (Doctoral Dissertation). Montpellier. Retrieved from http://www.theses.fr/2018MONTG086

Chicago Manual of Style (16th Edition):

Nhim, Sandra. “Mécanismes de régulation épigénétique chez l'insecte holocentrique ravageur de culture Spodoptera frugiperd, Lépidoptera, Noctuidae : Epigenetic regulation mecanisms in holocentric pest crop Spdoptera frugiperda, Lepidoptera, Noctuidae.” 2018. Doctoral Dissertation, Montpellier. Accessed May 22, 2019. http://www.theses.fr/2018MONTG086.

MLA Handbook (7th Edition):

Nhim, Sandra. “Mécanismes de régulation épigénétique chez l'insecte holocentrique ravageur de culture Spodoptera frugiperd, Lépidoptera, Noctuidae : Epigenetic regulation mecanisms in holocentric pest crop Spdoptera frugiperda, Lepidoptera, Noctuidae.” 2018. Web. 22 May 2019.

Vancouver:

Nhim S. Mécanismes de régulation épigénétique chez l'insecte holocentrique ravageur de culture Spodoptera frugiperd, Lépidoptera, Noctuidae : Epigenetic regulation mecanisms in holocentric pest crop Spdoptera frugiperda, Lepidoptera, Noctuidae. [Internet] [Doctoral dissertation]. Montpellier; 2018. [cited 2019 May 22]. Available from: http://www.theses.fr/2018MONTG086.

Council of Science Editors:

Nhim S. Mécanismes de régulation épigénétique chez l'insecte holocentrique ravageur de culture Spodoptera frugiperd, Lépidoptera, Noctuidae : Epigenetic regulation mecanisms in holocentric pest crop Spdoptera frugiperda, Lepidoptera, Noctuidae. [Doctoral Dissertation]. Montpellier; 2018. Available from: http://www.theses.fr/2018MONTG086


Penn State University

5. Rhee, Ho Sung. GENOME-WIDE ORGANIZATION OF TRANSCRIPTION MACHINERY DETECTED AT SINGLE NUCLEOTIDE RESOLUTION.

Degree: PhD, Biochemistry, Microbiology, and Molecular Biology, 2011, Penn State University

 Gene expression plays an important role in control of cell growth and differentiation in eukaryotic cells. Many proteins control gene expression by interacting with each… (more)

Subjects/Keywords: ChIP-seq; genomic binding locations; transcription factors

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APA (6th Edition):

Rhee, H. S. (2011). GENOME-WIDE ORGANIZATION OF TRANSCRIPTION MACHINERY DETECTED AT SINGLE NUCLEOTIDE RESOLUTION. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/12588

Chicago Manual of Style (16th Edition):

Rhee, Ho Sung. “GENOME-WIDE ORGANIZATION OF TRANSCRIPTION MACHINERY DETECTED AT SINGLE NUCLEOTIDE RESOLUTION.” 2011. Doctoral Dissertation, Penn State University. Accessed May 22, 2019. https://etda.libraries.psu.edu/catalog/12588.

MLA Handbook (7th Edition):

Rhee, Ho Sung. “GENOME-WIDE ORGANIZATION OF TRANSCRIPTION MACHINERY DETECTED AT SINGLE NUCLEOTIDE RESOLUTION.” 2011. Web. 22 May 2019.

Vancouver:

Rhee HS. GENOME-WIDE ORGANIZATION OF TRANSCRIPTION MACHINERY DETECTED AT SINGLE NUCLEOTIDE RESOLUTION. [Internet] [Doctoral dissertation]. Penn State University; 2011. [cited 2019 May 22]. Available from: https://etda.libraries.psu.edu/catalog/12588.

Council of Science Editors:

Rhee HS. GENOME-WIDE ORGANIZATION OF TRANSCRIPTION MACHINERY DETECTED AT SINGLE NUCLEOTIDE RESOLUTION. [Doctoral Dissertation]. Penn State University; 2011. Available from: https://etda.libraries.psu.edu/catalog/12588


Penn State University

6. Zhang, Zhenhai. DATAMINING OF GENOME-WIDE NUCLEOSOME DATA.

Degree: PhD, Integrative Biosciences, 2011, Penn State University

 The fundamental building block of eukaryotic genomes is the nucleosome, which consists of 147 base pairs DNA sequence and four core histones with possible exchange… (more)

Subjects/Keywords: Next-generation sequencing; data mining; ChIP-Seq

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APA (6th Edition):

Zhang, Z. (2011). DATAMINING OF GENOME-WIDE NUCLEOSOME DATA. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/11443

Chicago Manual of Style (16th Edition):

Zhang, Zhenhai. “DATAMINING OF GENOME-WIDE NUCLEOSOME DATA.” 2011. Doctoral Dissertation, Penn State University. Accessed May 22, 2019. https://etda.libraries.psu.edu/catalog/11443.

MLA Handbook (7th Edition):

Zhang, Zhenhai. “DATAMINING OF GENOME-WIDE NUCLEOSOME DATA.” 2011. Web. 22 May 2019.

Vancouver:

Zhang Z. DATAMINING OF GENOME-WIDE NUCLEOSOME DATA. [Internet] [Doctoral dissertation]. Penn State University; 2011. [cited 2019 May 22]. Available from: https://etda.libraries.psu.edu/catalog/11443.

Council of Science Editors:

Zhang Z. DATAMINING OF GENOME-WIDE NUCLEOSOME DATA. [Doctoral Dissertation]. Penn State University; 2011. Available from: https://etda.libraries.psu.edu/catalog/11443


University of California – Berkeley

7. Mayba, Oleg Sergeyevich. Statistical Aspects of ChIP-Seq Data Analysis.

Degree: Statistics, 2011, University of California – Berkeley

ChIP-Seq experiments combine the recently developed next-generation sequencing technology with the established chromatin immunoprecipitation assays to study the interactions between various classes of proteins and… (more)

Subjects/Keywords: Statistics; Bioinformatics; ChIP-Seq; peak-finding

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APA (6th Edition):

Mayba, O. S. (2011). Statistical Aspects of ChIP-Seq Data Analysis. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/1ss936z1

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Mayba, Oleg Sergeyevich. “Statistical Aspects of ChIP-Seq Data Analysis.” 2011. Thesis, University of California – Berkeley. Accessed May 22, 2019. http://www.escholarship.org/uc/item/1ss936z1.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Mayba, Oleg Sergeyevich. “Statistical Aspects of ChIP-Seq Data Analysis.” 2011. Web. 22 May 2019.

Vancouver:

Mayba OS. Statistical Aspects of ChIP-Seq Data Analysis. [Internet] [Thesis]. University of California – Berkeley; 2011. [cited 2019 May 22]. Available from: http://www.escholarship.org/uc/item/1ss936z1.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Mayba OS. Statistical Aspects of ChIP-Seq Data Analysis. [Thesis]. University of California – Berkeley; 2011. Available from: http://www.escholarship.org/uc/item/1ss936z1

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


UCLA

8. Kimball, Todd Haswell. ChI(r)P-seq: FoxP2 Binding Sites Uncover Molecular Mechanisms Influencing Songbird Vocalizations.

Degree: Physiological Science, 2018, UCLA

 The zebra finch, like humans, share a vocal learning phenotype and are an ideal model system to understand the molecular underpinnings of this multigenomic trait.… (more)

Subjects/Keywords: Physiology; ChIP-seq; FoxP2; Zebra Finch

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APA (6th Edition):

Kimball, T. H. (2018). ChI(r)P-seq: FoxP2 Binding Sites Uncover Molecular Mechanisms Influencing Songbird Vocalizations. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/8s18f8bj

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kimball, Todd Haswell. “ChI(r)P-seq: FoxP2 Binding Sites Uncover Molecular Mechanisms Influencing Songbird Vocalizations.” 2018. Thesis, UCLA. Accessed May 22, 2019. http://www.escholarship.org/uc/item/8s18f8bj.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kimball, Todd Haswell. “ChI(r)P-seq: FoxP2 Binding Sites Uncover Molecular Mechanisms Influencing Songbird Vocalizations.” 2018. Web. 22 May 2019.

Vancouver:

Kimball TH. ChI(r)P-seq: FoxP2 Binding Sites Uncover Molecular Mechanisms Influencing Songbird Vocalizations. [Internet] [Thesis]. UCLA; 2018. [cited 2019 May 22]. Available from: http://www.escholarship.org/uc/item/8s18f8bj.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kimball TH. ChI(r)P-seq: FoxP2 Binding Sites Uncover Molecular Mechanisms Influencing Songbird Vocalizations. [Thesis]. UCLA; 2018. Available from: http://www.escholarship.org/uc/item/8s18f8bj

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

9. Cauchy, Pierre. Rôle et contexte transcriptionnel du facteur de transcription Ets1 au cours transition CD4- CD8- à CD4+ CD8+ de la tymopoïèse αβ : Role and transcriptional context of the transcription factor Ets1 during αβ thymopoiesis.

Degree: Docteur es, Bioinformatique, biochimie structurale et génomique, 2010, Aix-Marseille 2

ETS1 est un facteur de transcription (FT) spécifique transposé dans les leucémies aigües. Le rôle essentiel d'ETS1 a été décrit au cours de l'hématopoïèse, plus… (more)

Subjects/Keywords: Bioinformatique; Thymopoïèse; Ets 1; ChIp-Seq

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APA (6th Edition):

Cauchy, P. (2010). Rôle et contexte transcriptionnel du facteur de transcription Ets1 au cours transition CD4- CD8- à CD4+ CD8+ de la tymopoïèse αβ : Role and transcriptional context of the transcription factor Ets1 during αβ thymopoiesis. (Doctoral Dissertation). Aix-Marseille 2. Retrieved from http://www.theses.fr/2010AIX22135

Chicago Manual of Style (16th Edition):

Cauchy, Pierre. “Rôle et contexte transcriptionnel du facteur de transcription Ets1 au cours transition CD4- CD8- à CD4+ CD8+ de la tymopoïèse αβ : Role and transcriptional context of the transcription factor Ets1 during αβ thymopoiesis.” 2010. Doctoral Dissertation, Aix-Marseille 2. Accessed May 22, 2019. http://www.theses.fr/2010AIX22135.

MLA Handbook (7th Edition):

Cauchy, Pierre. “Rôle et contexte transcriptionnel du facteur de transcription Ets1 au cours transition CD4- CD8- à CD4+ CD8+ de la tymopoïèse αβ : Role and transcriptional context of the transcription factor Ets1 during αβ thymopoiesis.” 2010. Web. 22 May 2019.

Vancouver:

Cauchy P. Rôle et contexte transcriptionnel du facteur de transcription Ets1 au cours transition CD4- CD8- à CD4+ CD8+ de la tymopoïèse αβ : Role and transcriptional context of the transcription factor Ets1 during αβ thymopoiesis. [Internet] [Doctoral dissertation]. Aix-Marseille 2; 2010. [cited 2019 May 22]. Available from: http://www.theses.fr/2010AIX22135.

Council of Science Editors:

Cauchy P. Rôle et contexte transcriptionnel du facteur de transcription Ets1 au cours transition CD4- CD8- à CD4+ CD8+ de la tymopoïèse αβ : Role and transcriptional context of the transcription factor Ets1 during αβ thymopoiesis. [Doctoral Dissertation]. Aix-Marseille 2; 2010. Available from: http://www.theses.fr/2010AIX22135


University of Minnesota

10. Yu, Shichao. A Simulation Study of Patient Accrual Patterns in Clinical Trials and Data Analysis of Histone 3 Lysine 36 Trimethylation ChIP-seq in Human Kidney Cancer.

Degree: MS, Biomedical Informatics and Computational Biology, 2017, University of Minnesota

 In part one, we simulated a successive of two-armed randomized clinical trial with the time-to-event outcome over 15 years. We used three different accrual pattern… (more)

Subjects/Keywords: ChIP-Seq; Clinical trial; Normalization; Simulation

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APA (6th Edition):

Yu, S. (2017). A Simulation Study of Patient Accrual Patterns in Clinical Trials and Data Analysis of Histone 3 Lysine 36 Trimethylation ChIP-seq in Human Kidney Cancer. (Masters Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/191226

Chicago Manual of Style (16th Edition):

Yu, Shichao. “A Simulation Study of Patient Accrual Patterns in Clinical Trials and Data Analysis of Histone 3 Lysine 36 Trimethylation ChIP-seq in Human Kidney Cancer.” 2017. Masters Thesis, University of Minnesota. Accessed May 22, 2019. http://hdl.handle.net/11299/191226.

MLA Handbook (7th Edition):

Yu, Shichao. “A Simulation Study of Patient Accrual Patterns in Clinical Trials and Data Analysis of Histone 3 Lysine 36 Trimethylation ChIP-seq in Human Kidney Cancer.” 2017. Web. 22 May 2019.

Vancouver:

Yu S. A Simulation Study of Patient Accrual Patterns in Clinical Trials and Data Analysis of Histone 3 Lysine 36 Trimethylation ChIP-seq in Human Kidney Cancer. [Internet] [Masters thesis]. University of Minnesota; 2017. [cited 2019 May 22]. Available from: http://hdl.handle.net/11299/191226.

Council of Science Editors:

Yu S. A Simulation Study of Patient Accrual Patterns in Clinical Trials and Data Analysis of Histone 3 Lysine 36 Trimethylation ChIP-seq in Human Kidney Cancer. [Masters Thesis]. University of Minnesota; 2017. Available from: http://hdl.handle.net/11299/191226

11. Silva, Vinicius Henrique da. Identification of CNVs in the Nelore genome and its association with meat tenderness.

Degree: Mestrado, Ciência Animal e Pastagens, 2015, University of São Paulo

The Nelore breed represents the vast majority of Brazilian Zebuine cattle (Bos taurus indicus). The great adaptability of the Nelore breed to Brazilian tropical climate,… (more)

Subjects/Keywords: Genome-wide; Integração; Integration; Pangenômico; RNA-seq; RNA-seq; SNP-chip; SNP-chip

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APA (6th Edition):

Silva, V. H. d. (2015). Identification of CNVs in the Nelore genome and its association with meat tenderness. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/11/11139/tde-22042015-134017/ ;

Chicago Manual of Style (16th Edition):

Silva, Vinicius Henrique da. “Identification of CNVs in the Nelore genome and its association with meat tenderness.” 2015. Masters Thesis, University of São Paulo. Accessed May 22, 2019. http://www.teses.usp.br/teses/disponiveis/11/11139/tde-22042015-134017/ ;.

MLA Handbook (7th Edition):

Silva, Vinicius Henrique da. “Identification of CNVs in the Nelore genome and its association with meat tenderness.” 2015. Web. 22 May 2019.

Vancouver:

Silva VHd. Identification of CNVs in the Nelore genome and its association with meat tenderness. [Internet] [Masters thesis]. University of São Paulo; 2015. [cited 2019 May 22]. Available from: http://www.teses.usp.br/teses/disponiveis/11/11139/tde-22042015-134017/ ;.

Council of Science Editors:

Silva VHd. Identification of CNVs in the Nelore genome and its association with meat tenderness. [Masters Thesis]. University of São Paulo; 2015. Available from: http://www.teses.usp.br/teses/disponiveis/11/11139/tde-22042015-134017/ ;


Université de Montréal

12. Mercier, Eloi. Développement d’outils pour l’analyse de données de ChIP-seq et l’identification des facteurs de transcription .

Degree: 2011, Université de Montréal

 La méthode ChIP-seq est une technologie combinant la technique de chromatine immunoprecipitation avec le séquençage haut-débit et permettant l’analyse in vivo des facteurs de transcription… (more)

Subjects/Keywords: Génétique; Régulation; Facteur de transcription; ChIP-seq; Genetics; Regulation; Transcription Factors; ChIP-seq

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APA (6th Edition):

Mercier, E. (2011). Développement d’outils pour l’analyse de données de ChIP-seq et l’identification des facteurs de transcription . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/6038

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Mercier, Eloi. “Développement d’outils pour l’analyse de données de ChIP-seq et l’identification des facteurs de transcription .” 2011. Thesis, Université de Montréal. Accessed May 22, 2019. http://hdl.handle.net/1866/6038.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Mercier, Eloi. “Développement d’outils pour l’analyse de données de ChIP-seq et l’identification des facteurs de transcription .” 2011. Web. 22 May 2019.

Vancouver:

Mercier E. Développement d’outils pour l’analyse de données de ChIP-seq et l’identification des facteurs de transcription . [Internet] [Thesis]. Université de Montréal; 2011. [cited 2019 May 22]. Available from: http://hdl.handle.net/1866/6038.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Mercier E. Développement d’outils pour l’analyse de données de ChIP-seq et l’identification des facteurs de transcription . [Thesis]. Université de Montréal; 2011. Available from: http://hdl.handle.net/1866/6038

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

13. Samuel, Alexander. Étude génomique des fonctions du facteur de transcription Otx2 dans la rétine de souris adulte : Genomic study of Otx2 transcription factor functions in the adult mouse retina.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2013, Nice

Pour comprendre comment les gènes du développement exercent de multiples fonctions temporelles, nous prenons comme modèle le facteur de transcription Otx2. Celui-ci est impliqué dans… (more)

Subjects/Keywords: Otx2; Rétine; ChIP-seq; Transcriptome; Complexes protéiques; Otx2; Retina; ChIP-seq; Transcriptome; Protein complexes

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APA (6th Edition):

Samuel, A. (2013). Étude génomique des fonctions du facteur de transcription Otx2 dans la rétine de souris adulte : Genomic study of Otx2 transcription factor functions in the adult mouse retina. (Doctoral Dissertation). Nice. Retrieved from http://www.theses.fr/2013NICE4125

Chicago Manual of Style (16th Edition):

Samuel, Alexander. “Étude génomique des fonctions du facteur de transcription Otx2 dans la rétine de souris adulte : Genomic study of Otx2 transcription factor functions in the adult mouse retina.” 2013. Doctoral Dissertation, Nice. Accessed May 22, 2019. http://www.theses.fr/2013NICE4125.

MLA Handbook (7th Edition):

Samuel, Alexander. “Étude génomique des fonctions du facteur de transcription Otx2 dans la rétine de souris adulte : Genomic study of Otx2 transcription factor functions in the adult mouse retina.” 2013. Web. 22 May 2019.

Vancouver:

Samuel A. Étude génomique des fonctions du facteur de transcription Otx2 dans la rétine de souris adulte : Genomic study of Otx2 transcription factor functions in the adult mouse retina. [Internet] [Doctoral dissertation]. Nice; 2013. [cited 2019 May 22]. Available from: http://www.theses.fr/2013NICE4125.

Council of Science Editors:

Samuel A. Étude génomique des fonctions du facteur de transcription Otx2 dans la rétine de souris adulte : Genomic study of Otx2 transcription factor functions in the adult mouse retina. [Doctoral Dissertation]. Nice; 2013. Available from: http://www.theses.fr/2013NICE4125

14. Fant, Bruno. Importance du contexte cellulaire et de la régulation spatio-temporelle de l'expression du facteur de transcription Otx2 dans la modulation de ses fonctions : The importance of cellular context and of regulation of expression in modulating the functions of Otx2.

Degree: Docteur es, Interactions moléculaires et cellulaires, 2014, Nice

Cette thèse s’intéresse aux mécanismes permettant d’expliquer plusieurs des fonctions de l’homéogène Otx2 au cours du développement. Une première partie étudie l’importance de la régulation… (more)

Subjects/Keywords: Otx2; MHB; Rétine; Protéomique; ChIP-seq; Otx2; MHB; Retina; Proteomics; ChIP-seq

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APA (6th Edition):

Fant, B. (2014). Importance du contexte cellulaire et de la régulation spatio-temporelle de l'expression du facteur de transcription Otx2 dans la modulation de ses fonctions : The importance of cellular context and of regulation of expression in modulating the functions of Otx2. (Doctoral Dissertation). Nice. Retrieved from http://www.theses.fr/2014NICE4100

Chicago Manual of Style (16th Edition):

Fant, Bruno. “Importance du contexte cellulaire et de la régulation spatio-temporelle de l'expression du facteur de transcription Otx2 dans la modulation de ses fonctions : The importance of cellular context and of regulation of expression in modulating the functions of Otx2.” 2014. Doctoral Dissertation, Nice. Accessed May 22, 2019. http://www.theses.fr/2014NICE4100.

MLA Handbook (7th Edition):

Fant, Bruno. “Importance du contexte cellulaire et de la régulation spatio-temporelle de l'expression du facteur de transcription Otx2 dans la modulation de ses fonctions : The importance of cellular context and of regulation of expression in modulating the functions of Otx2.” 2014. Web. 22 May 2019.

Vancouver:

Fant B. Importance du contexte cellulaire et de la régulation spatio-temporelle de l'expression du facteur de transcription Otx2 dans la modulation de ses fonctions : The importance of cellular context and of regulation of expression in modulating the functions of Otx2. [Internet] [Doctoral dissertation]. Nice; 2014. [cited 2019 May 22]. Available from: http://www.theses.fr/2014NICE4100.

Council of Science Editors:

Fant B. Importance du contexte cellulaire et de la régulation spatio-temporelle de l'expression du facteur de transcription Otx2 dans la modulation de ses fonctions : The importance of cellular context and of regulation of expression in modulating the functions of Otx2. [Doctoral Dissertation]. Nice; 2014. Available from: http://www.theses.fr/2014NICE4100

15. Pascali, Chiara. Identification à l'échelle génomique de gènes transcrits par deux isoformes de l'ARN polymérase III humaine : Genome wide identification of genes transcribed by two isoforms of human RNA.

Degree: Docteur es, Sciences, technologie, santé. Génétique, 2011, Université de Bordeaux Segalen

En 2010, Haurie et al. ont identifié deux isoformes différentes de la Pol III humaine : Pol IIIα, quin’est présente que dans les cellules souches… (more)

Subjects/Keywords: Homme; Cancer; Polymérase III; Transcription; ChIP-Seq; Human; Cancer; Pol III; Transcription; ChIP-Seq

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APA (6th Edition):

Pascali, C. (2011). Identification à l'échelle génomique de gènes transcrits par deux isoformes de l'ARN polymérase III humaine : Genome wide identification of genes transcribed by two isoforms of human RNA. (Doctoral Dissertation). Université de Bordeaux Segalen. Retrieved from http://www.theses.fr/2011BOR21813

Chicago Manual of Style (16th Edition):

Pascali, Chiara. “Identification à l'échelle génomique de gènes transcrits par deux isoformes de l'ARN polymérase III humaine : Genome wide identification of genes transcribed by two isoforms of human RNA.” 2011. Doctoral Dissertation, Université de Bordeaux Segalen. Accessed May 22, 2019. http://www.theses.fr/2011BOR21813.

MLA Handbook (7th Edition):

Pascali, Chiara. “Identification à l'échelle génomique de gènes transcrits par deux isoformes de l'ARN polymérase III humaine : Genome wide identification of genes transcribed by two isoforms of human RNA.” 2011. Web. 22 May 2019.

Vancouver:

Pascali C. Identification à l'échelle génomique de gènes transcrits par deux isoformes de l'ARN polymérase III humaine : Genome wide identification of genes transcribed by two isoforms of human RNA. [Internet] [Doctoral dissertation]. Université de Bordeaux Segalen; 2011. [cited 2019 May 22]. Available from: http://www.theses.fr/2011BOR21813.

Council of Science Editors:

Pascali C. Identification à l'échelle génomique de gènes transcrits par deux isoformes de l'ARN polymérase III humaine : Genome wide identification of genes transcribed by two isoforms of human RNA. [Doctoral Dissertation]. Université de Bordeaux Segalen; 2011. Available from: http://www.theses.fr/2011BOR21813


Duke University

16. Luo, Kaixuan. Modeling Nuclease Digestion Data to Predict the Dynamics of Genome-wide Transcription Factor Occupancy .

Degree: 2016, Duke University

  Identifying and deciphering the complex regulatory information embedded in the genome is critical to our understanding of biology and the etiology of complex diseases.… (more)

Subjects/Keywords: Bioinformatics; Genetics; Bayesian hierarchical model; ChIP-seq; DNase-seq; gene regulation; MNase-seq; transcription factors

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APA (6th Edition):

Luo, K. (2016). Modeling Nuclease Digestion Data to Predict the Dynamics of Genome-wide Transcription Factor Occupancy . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/14351

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Luo, Kaixuan. “Modeling Nuclease Digestion Data to Predict the Dynamics of Genome-wide Transcription Factor Occupancy .” 2016. Thesis, Duke University. Accessed May 22, 2019. http://hdl.handle.net/10161/14351.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Luo, Kaixuan. “Modeling Nuclease Digestion Data to Predict the Dynamics of Genome-wide Transcription Factor Occupancy .” 2016. Web. 22 May 2019.

Vancouver:

Luo K. Modeling Nuclease Digestion Data to Predict the Dynamics of Genome-wide Transcription Factor Occupancy . [Internet] [Thesis]. Duke University; 2016. [cited 2019 May 22]. Available from: http://hdl.handle.net/10161/14351.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Luo K. Modeling Nuclease Digestion Data to Predict the Dynamics of Genome-wide Transcription Factor Occupancy . [Thesis]. Duke University; 2016. Available from: http://hdl.handle.net/10161/14351

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of California – Irvine

17. Le, Rebekah Charney. The role of maternal Foxh1 in the activation of the mesendoderm gene regulatory network.

Degree: Biological Sciences, 2016, University of California – Irvine

 Germ layer specification is one of the earliest developmental events in metazoan organisms, and relies upon the combinatorial interactions of signaling pathways and transcription factors… (more)

Subjects/Keywords: Developmental biology; ChIP-seq; endoderm; Foxh1; Groucho/Tle; RNA-seq; Xenopus

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APA (6th Edition):

Le, R. C. (2016). The role of maternal Foxh1 in the activation of the mesendoderm gene regulatory network. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/22r462c6

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Le, Rebekah Charney. “The role of maternal Foxh1 in the activation of the mesendoderm gene regulatory network.” 2016. Thesis, University of California – Irvine. Accessed May 22, 2019. http://www.escholarship.org/uc/item/22r462c6.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Le, Rebekah Charney. “The role of maternal Foxh1 in the activation of the mesendoderm gene regulatory network.” 2016. Web. 22 May 2019.

Vancouver:

Le RC. The role of maternal Foxh1 in the activation of the mesendoderm gene regulatory network. [Internet] [Thesis]. University of California – Irvine; 2016. [cited 2019 May 22]. Available from: http://www.escholarship.org/uc/item/22r462c6.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Le RC. The role of maternal Foxh1 in the activation of the mesendoderm gene regulatory network. [Thesis]. University of California – Irvine; 2016. Available from: http://www.escholarship.org/uc/item/22r462c6

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of California – Berkeley

18. Roberts, Adam. Ambiguous fragment assignment for high-throughput sequencing experiments.

Degree: Computer Science, 2013, University of California – Berkeley

 As the cost of short-read, high-throughput DNA sequencing continues to fall rapidly, new uses for the technology have been developed aside from its original purpose… (more)

Subjects/Keywords: Computer science; Bioinformatics; chip-seq; expectation-maximization; rna-seq; sequencing

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APA (6th Edition):

Roberts, A. (2013). Ambiguous fragment assignment for high-throughput sequencing experiments. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/7zx1s4hr

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Roberts, Adam. “Ambiguous fragment assignment for high-throughput sequencing experiments.” 2013. Thesis, University of California – Berkeley. Accessed May 22, 2019. http://www.escholarship.org/uc/item/7zx1s4hr.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Roberts, Adam. “Ambiguous fragment assignment for high-throughput sequencing experiments.” 2013. Web. 22 May 2019.

Vancouver:

Roberts A. Ambiguous fragment assignment for high-throughput sequencing experiments. [Internet] [Thesis]. University of California – Berkeley; 2013. [cited 2019 May 22]. Available from: http://www.escholarship.org/uc/item/7zx1s4hr.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Roberts A. Ambiguous fragment assignment for high-throughput sequencing experiments. [Thesis]. University of California – Berkeley; 2013. Available from: http://www.escholarship.org/uc/item/7zx1s4hr

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

19. Sugathan, Aarathi. Role of growth hormone and chromatin structure in regulation of sex differences in mouse liver gene expression.

Degree: PhD, Bioinformatics, 2013, Boston University

 Sex differences in mammalian gene expression result from differences in genotypic sex as well as in hormonal regulators between males and females. In rat, mouse… (more)

Subjects/Keywords: Bioinformatics; ChIP-seq; DNase-seq; Epigenomics; Liver sexual dimorphism

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APA (6th Edition):

Sugathan, A. (2013). Role of growth hormone and chromatin structure in regulation of sex differences in mouse liver gene expression. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/13139

Chicago Manual of Style (16th Edition):

Sugathan, Aarathi. “Role of growth hormone and chromatin structure in regulation of sex differences in mouse liver gene expression.” 2013. Doctoral Dissertation, Boston University. Accessed May 22, 2019. http://hdl.handle.net/2144/13139.

MLA Handbook (7th Edition):

Sugathan, Aarathi. “Role of growth hormone and chromatin structure in regulation of sex differences in mouse liver gene expression.” 2013. Web. 22 May 2019.

Vancouver:

Sugathan A. Role of growth hormone and chromatin structure in regulation of sex differences in mouse liver gene expression. [Internet] [Doctoral dissertation]. Boston University; 2013. [cited 2019 May 22]. Available from: http://hdl.handle.net/2144/13139.

Council of Science Editors:

Sugathan A. Role of growth hormone and chromatin structure in regulation of sex differences in mouse liver gene expression. [Doctoral Dissertation]. Boston University; 2013. Available from: http://hdl.handle.net/2144/13139


Rochester Institute of Technology

20. Freewoman, Julia. Identification of Differential Expression of p53 associated RNAs at 3 Different Treatment Timepoints, and Association with ChIP-seq Identified p53 Genes.

Degree: MS, Thomas H. Gosnell School of Life Sciences (COS), 2017, Rochester Institute of Technology

  Called “the guardian of the genome,” p53 is one of the most studied proteins associated with cancer. After activation, p53 induces its target genes… (more)

Subjects/Keywords: 5-fluorouracil; ChIP-seq; p53; RNA-seq; Time course

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APA (6th Edition):

Freewoman, J. (2017). Identification of Differential Expression of p53 associated RNAs at 3 Different Treatment Timepoints, and Association with ChIP-seq Identified p53 Genes. (Masters Thesis). Rochester Institute of Technology. Retrieved from https://scholarworks.rit.edu/theses/9489

Chicago Manual of Style (16th Edition):

Freewoman, Julia. “Identification of Differential Expression of p53 associated RNAs at 3 Different Treatment Timepoints, and Association with ChIP-seq Identified p53 Genes.” 2017. Masters Thesis, Rochester Institute of Technology. Accessed May 22, 2019. https://scholarworks.rit.edu/theses/9489.

MLA Handbook (7th Edition):

Freewoman, Julia. “Identification of Differential Expression of p53 associated RNAs at 3 Different Treatment Timepoints, and Association with ChIP-seq Identified p53 Genes.” 2017. Web. 22 May 2019.

Vancouver:

Freewoman J. Identification of Differential Expression of p53 associated RNAs at 3 Different Treatment Timepoints, and Association with ChIP-seq Identified p53 Genes. [Internet] [Masters thesis]. Rochester Institute of Technology; 2017. [cited 2019 May 22]. Available from: https://scholarworks.rit.edu/theses/9489.

Council of Science Editors:

Freewoman J. Identification of Differential Expression of p53 associated RNAs at 3 Different Treatment Timepoints, and Association with ChIP-seq Identified p53 Genes. [Masters Thesis]. Rochester Institute of Technology; 2017. Available from: https://scholarworks.rit.edu/theses/9489


University of Southern California

21. Dai, Chao. Integrating high-throughput sequencing data to study gene regulation.

Degree: PhD, Computational Biology and Bioinformatics, 2015, University of Southern California

 High-throughput sequencing is a powerful technique for gene regulation study, which can provide information about isoform expression as well as transcription factors / epigenetic factors… (more)

Subjects/Keywords: gene regulation; RNA-seq; ChIP-seq; spatial genome organization

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APA (6th Edition):

Dai, C. (2015). Integrating high-throughput sequencing data to study gene regulation. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/340117/rec/3533

Chicago Manual of Style (16th Edition):

Dai, Chao. “Integrating high-throughput sequencing data to study gene regulation.” 2015. Doctoral Dissertation, University of Southern California. Accessed May 22, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/340117/rec/3533.

MLA Handbook (7th Edition):

Dai, Chao. “Integrating high-throughput sequencing data to study gene regulation.” 2015. Web. 22 May 2019.

Vancouver:

Dai C. Integrating high-throughput sequencing data to study gene regulation. [Internet] [Doctoral dissertation]. University of Southern California; 2015. [cited 2019 May 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/340117/rec/3533.

Council of Science Editors:

Dai C. Integrating high-throughput sequencing data to study gene regulation. [Doctoral Dissertation]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/340117/rec/3533


Université Paris-Sud – Paris XI

22. Torre, Cyril. Analyse haut-débit des complexes transcriptionnels de la β-caténine dans le foie murin : High-throughput analysis of β-catenin dependant transcriptional complex in the murin liver.

Degree: Docteur es, Cancérologie, 2011, Université Paris-Sud – Paris XI

 La voie Wnt/β-caténine est impliquée dans la prolifération et le contrôle du destin cellulaire de nombreux tissus à la fois au cours du développement et… (more)

Subjects/Keywords: Sono-seq; ChIp-seq; Zonage métabolique; Génome analyser

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APA (6th Edition):

Torre, C. (2011). Analyse haut-débit des complexes transcriptionnels de la β-caténine dans le foie murin : High-throughput analysis of β-catenin dependant transcriptional complex in the murin liver. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2011PA11T004

Chicago Manual of Style (16th Edition):

Torre, Cyril. “Analyse haut-débit des complexes transcriptionnels de la β-caténine dans le foie murin : High-throughput analysis of β-catenin dependant transcriptional complex in the murin liver.” 2011. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed May 22, 2019. http://www.theses.fr/2011PA11T004.

MLA Handbook (7th Edition):

Torre, Cyril. “Analyse haut-débit des complexes transcriptionnels de la β-caténine dans le foie murin : High-throughput analysis of β-catenin dependant transcriptional complex in the murin liver.” 2011. Web. 22 May 2019.

Vancouver:

Torre C. Analyse haut-débit des complexes transcriptionnels de la β-caténine dans le foie murin : High-throughput analysis of β-catenin dependant transcriptional complex in the murin liver. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2011. [cited 2019 May 22]. Available from: http://www.theses.fr/2011PA11T004.

Council of Science Editors:

Torre C. Analyse haut-débit des complexes transcriptionnels de la β-caténine dans le foie murin : High-throughput analysis of β-catenin dependant transcriptional complex in the murin liver. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2011. Available from: http://www.theses.fr/2011PA11T004


University of Minnesota

23. Lee, Catherine Ann Alsager. Isolation and identification of De Novo long noncoding RNAs from mouse myoblasts and embryonic stem cells.

Degree: MS, Stem Cell Biology, 2013, University of Minnesota

University of Minnesota M.S. thesis. January 2013. Major: Stem Cell Biology. Advisor: Nobuaki Kikyo. 1 computer file (PDF); vii, 46 pages.

Long noncoding RNAs (lncRNAs)… (more)

Subjects/Keywords: ChIP; MyoD; Pluripotency; RNA-ChIP; RNA-seq; Trithorax-group

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APA (6th Edition):

Lee, C. A. A. (2013). Isolation and identification of De Novo long noncoding RNAs from mouse myoblasts and embryonic stem cells. (Masters Thesis). University of Minnesota. Retrieved from http://purl.umn.edu/146424

Chicago Manual of Style (16th Edition):

Lee, Catherine Ann Alsager. “Isolation and identification of De Novo long noncoding RNAs from mouse myoblasts and embryonic stem cells.” 2013. Masters Thesis, University of Minnesota. Accessed May 22, 2019. http://purl.umn.edu/146424.

MLA Handbook (7th Edition):

Lee, Catherine Ann Alsager. “Isolation and identification of De Novo long noncoding RNAs from mouse myoblasts and embryonic stem cells.” 2013. Web. 22 May 2019.

Vancouver:

Lee CAA. Isolation and identification of De Novo long noncoding RNAs from mouse myoblasts and embryonic stem cells. [Internet] [Masters thesis]. University of Minnesota; 2013. [cited 2019 May 22]. Available from: http://purl.umn.edu/146424.

Council of Science Editors:

Lee CAA. Isolation and identification of De Novo long noncoding RNAs from mouse myoblasts and embryonic stem cells. [Masters Thesis]. University of Minnesota; 2013. Available from: http://purl.umn.edu/146424


University of Minnesota

24. Lee, Catherine Ann Alsager. Isolation and identification of De Novo long noncoding RNAs from mouse myoblasts and embryonic stem cells.

Degree: MS, Stem Cell Biology, 2013, University of Minnesota

 Long noncoding RNAs (lncRNAs) are a pervasive class of transcripts whose importance and biological relevance are only beginning to be elucidated. LncRNAs have been detected… (more)

Subjects/Keywords: ChIP; MyoD; Pluripotency; RNA-ChIP; RNA-seq; Trithorax-group

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APA (6th Edition):

Lee, C. A. A. (2013). Isolation and identification of De Novo long noncoding RNAs from mouse myoblasts and embryonic stem cells. (Masters Thesis). University of Minnesota. Retrieved from http://purl.umn.edu/146424

Chicago Manual of Style (16th Edition):

Lee, Catherine Ann Alsager. “Isolation and identification of De Novo long noncoding RNAs from mouse myoblasts and embryonic stem cells.” 2013. Masters Thesis, University of Minnesota. Accessed May 22, 2019. http://purl.umn.edu/146424.

MLA Handbook (7th Edition):

Lee, Catherine Ann Alsager. “Isolation and identification of De Novo long noncoding RNAs from mouse myoblasts and embryonic stem cells.” 2013. Web. 22 May 2019.

Vancouver:

Lee CAA. Isolation and identification of De Novo long noncoding RNAs from mouse myoblasts and embryonic stem cells. [Internet] [Masters thesis]. University of Minnesota; 2013. [cited 2019 May 22]. Available from: http://purl.umn.edu/146424.

Council of Science Editors:

Lee CAA. Isolation and identification of De Novo long noncoding RNAs from mouse myoblasts and embryonic stem cells. [Masters Thesis]. University of Minnesota; 2013. Available from: http://purl.umn.edu/146424

25. Strasser, Perrine. Rôle du facteur de transcription RFX6 dans la différenciation et la fonction des cellules β sécrétrices d'insuline : identification et étude de gènes cibles : Role of the RFX6 transcription factor in insulin secreting beta cells differenciation and function : identification and study of target genes.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2015, Université de Strasbourg

La régulation de l’homéostasie du glucose dans l’organisme est la fonction principale des cellules beta sécrétrices d’insuline dans le pancréas endocrine. Le facteur de transcription… (more)

Subjects/Keywords: RFX6; Cellules beta; Pancréas; Insuline; ChIP Seq; Diabète; RNA Seq; MLXIPL; RFX6; Beta cells; Pancreatic islets; Insulin; ChIP Seq; Diabetes; RNA Seq; MLXIPL; 571.86; 572.8; 616.4

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Strasser, P. (2015). Rôle du facteur de transcription RFX6 dans la différenciation et la fonction des cellules β sécrétrices d'insuline : identification et étude de gènes cibles : Role of the RFX6 transcription factor in insulin secreting beta cells differenciation and function : identification and study of target genes. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2015STRAJ088

Chicago Manual of Style (16th Edition):

Strasser, Perrine. “Rôle du facteur de transcription RFX6 dans la différenciation et la fonction des cellules β sécrétrices d'insuline : identification et étude de gènes cibles : Role of the RFX6 transcription factor in insulin secreting beta cells differenciation and function : identification and study of target genes.” 2015. Doctoral Dissertation, Université de Strasbourg. Accessed May 22, 2019. http://www.theses.fr/2015STRAJ088.

MLA Handbook (7th Edition):

Strasser, Perrine. “Rôle du facteur de transcription RFX6 dans la différenciation et la fonction des cellules β sécrétrices d'insuline : identification et étude de gènes cibles : Role of the RFX6 transcription factor in insulin secreting beta cells differenciation and function : identification and study of target genes.” 2015. Web. 22 May 2019.

Vancouver:

Strasser P. Rôle du facteur de transcription RFX6 dans la différenciation et la fonction des cellules β sécrétrices d'insuline : identification et étude de gènes cibles : Role of the RFX6 transcription factor in insulin secreting beta cells differenciation and function : identification and study of target genes. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2015. [cited 2019 May 22]. Available from: http://www.theses.fr/2015STRAJ088.

Council of Science Editors:

Strasser P. Rôle du facteur de transcription RFX6 dans la différenciation et la fonction des cellules β sécrétrices d'insuline : identification et étude de gènes cibles : Role of the RFX6 transcription factor in insulin secreting beta cells differenciation and function : identification and study of target genes. [Doctoral Dissertation]. Université de Strasbourg; 2015. Available from: http://www.theses.fr/2015STRAJ088

26. Descostes, Nicolas. Analyse bioinformatique des modifications post-traductionnelles du domaine carboxyl-terminal de l'Arn polymérase II : Bioinformatic analysis of post-translational modifications of the carboxy-terminal domain of RNA polymerase II.

Degree: Docteur es, Biologie. Bioinformatique et génomique, 2014, Aix Marseille Université

Le processus transcriptionnel par l'ARN polymérase II (Pol II) chez les eucaryotes se déroule en trois étapes : L'initiation, l'élongation et la terminaison. De nombreux… (more)

Subjects/Keywords: ARN Polymerase II; Transcription; Ctd; Bioinformatique; Séquençage; Chip-Seq; Rna-Seq; Génomique; RNA polymerase II; Transcription; Ctd; Bioinformatics; Sequencing; Chip-Seq; Rna-Seq; Genomics; 570

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APA (6th Edition):

Descostes, N. (2014). Analyse bioinformatique des modifications post-traductionnelles du domaine carboxyl-terminal de l'Arn polymérase II : Bioinformatic analysis of post-translational modifications of the carboxy-terminal domain of RNA polymerase II. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2014AIXM4089

Chicago Manual of Style (16th Edition):

Descostes, Nicolas. “Analyse bioinformatique des modifications post-traductionnelles du domaine carboxyl-terminal de l'Arn polymérase II : Bioinformatic analysis of post-translational modifications of the carboxy-terminal domain of RNA polymerase II.” 2014. Doctoral Dissertation, Aix Marseille Université. Accessed May 22, 2019. http://www.theses.fr/2014AIXM4089.

MLA Handbook (7th Edition):

Descostes, Nicolas. “Analyse bioinformatique des modifications post-traductionnelles du domaine carboxyl-terminal de l'Arn polymérase II : Bioinformatic analysis of post-translational modifications of the carboxy-terminal domain of RNA polymerase II.” 2014. Web. 22 May 2019.

Vancouver:

Descostes N. Analyse bioinformatique des modifications post-traductionnelles du domaine carboxyl-terminal de l'Arn polymérase II : Bioinformatic analysis of post-translational modifications of the carboxy-terminal domain of RNA polymerase II. [Internet] [Doctoral dissertation]. Aix Marseille Université 2014. [cited 2019 May 22]. Available from: http://www.theses.fr/2014AIXM4089.

Council of Science Editors:

Descostes N. Analyse bioinformatique des modifications post-traductionnelles du domaine carboxyl-terminal de l'Arn polymérase II : Bioinformatic analysis of post-translational modifications of the carboxy-terminal domain of RNA polymerase II. [Doctoral Dissertation]. Aix Marseille Université 2014. Available from: http://www.theses.fr/2014AIXM4089

27. Hao, Chunxiang. The impacts of the widely used herbicide atrazine on epigenetic processes of meiosis and transgenerational inheritance : Impact d’un herbicide largement utilisé, l’atrazine, sur les régulations épigénétiques de la méiose et l’héritage transgénérationel.

Degree: Docteur es, Biologie, 2016, Rennes 1

 Les facteurs environnementaux, tels que les pesticides, peuvent induire des changements phénotypiques dans une variété d'organisme incluant les mammifères. Nous avons étudié chez la souris… (more)

Subjects/Keywords: ChIP-Seq; H3K4me3; ARN-Seq; Alternative initiation de la transcription; L'héritage transgénérationnel; ChIP-Seq; H3K4me3; RNA-Seq; Alternative transcription initiation; Transgenerational inheritance

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APA (6th Edition):

Hao, C. (2016). The impacts of the widely used herbicide atrazine on epigenetic processes of meiosis and transgenerational inheritance : Impact d’un herbicide largement utilisé, l’atrazine, sur les régulations épigénétiques de la méiose et l’héritage transgénérationel. (Doctoral Dissertation). Rennes 1. Retrieved from http://www.theses.fr/2016REN1B007

Chicago Manual of Style (16th Edition):

Hao, Chunxiang. “The impacts of the widely used herbicide atrazine on epigenetic processes of meiosis and transgenerational inheritance : Impact d’un herbicide largement utilisé, l’atrazine, sur les régulations épigénétiques de la méiose et l’héritage transgénérationel.” 2016. Doctoral Dissertation, Rennes 1. Accessed May 22, 2019. http://www.theses.fr/2016REN1B007.

MLA Handbook (7th Edition):

Hao, Chunxiang. “The impacts of the widely used herbicide atrazine on epigenetic processes of meiosis and transgenerational inheritance : Impact d’un herbicide largement utilisé, l’atrazine, sur les régulations épigénétiques de la méiose et l’héritage transgénérationel.” 2016. Web. 22 May 2019.

Vancouver:

Hao C. The impacts of the widely used herbicide atrazine on epigenetic processes of meiosis and transgenerational inheritance : Impact d’un herbicide largement utilisé, l’atrazine, sur les régulations épigénétiques de la méiose et l’héritage transgénérationel. [Internet] [Doctoral dissertation]. Rennes 1; 2016. [cited 2019 May 22]. Available from: http://www.theses.fr/2016REN1B007.

Council of Science Editors:

Hao C. The impacts of the widely used herbicide atrazine on epigenetic processes of meiosis and transgenerational inheritance : Impact d’un herbicide largement utilisé, l’atrazine, sur les régulations épigénétiques de la méiose et l’héritage transgénérationel. [Doctoral Dissertation]. Rennes 1; 2016. Available from: http://www.theses.fr/2016REN1B007


Université de Sherbrooke

28. Berthoumieux, Mélodie. Étude pangénomique des sites de liaison de la protéine Rnt1p et de son rôle dans la maturation des snoARN chez Saccharomyces cerevisiae .

Degree: 2019, Université de Sherbrooke

 La ribonucléase III de la levure Saccharomyces cerevisiae, Rnt1p est connue pour ses rôles multiples dans la maturation des acides ribonucléiques (ARN) non codants et… (more)

Subjects/Keywords: RNA-seq; ChIP-seq; Ribonuclease III; Transcription; Maturation; Ribonucléase III; SnoARN; SnoRNA

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Berthoumieux, M. (2019). Étude pangénomique des sites de liaison de la protéine Rnt1p et de son rôle dans la maturation des snoARN chez Saccharomyces cerevisiae . (Masters Thesis). Université de Sherbrooke. Retrieved from http://hdl.handle.net/11143/15200

Chicago Manual of Style (16th Edition):

Berthoumieux, Mélodie. “Étude pangénomique des sites de liaison de la protéine Rnt1p et de son rôle dans la maturation des snoARN chez Saccharomyces cerevisiae .” 2019. Masters Thesis, Université de Sherbrooke. Accessed May 22, 2019. http://hdl.handle.net/11143/15200.

MLA Handbook (7th Edition):

Berthoumieux, Mélodie. “Étude pangénomique des sites de liaison de la protéine Rnt1p et de son rôle dans la maturation des snoARN chez Saccharomyces cerevisiae .” 2019. Web. 22 May 2019.

Vancouver:

Berthoumieux M. Étude pangénomique des sites de liaison de la protéine Rnt1p et de son rôle dans la maturation des snoARN chez Saccharomyces cerevisiae . [Internet] [Masters thesis]. Université de Sherbrooke; 2019. [cited 2019 May 22]. Available from: http://hdl.handle.net/11143/15200.

Council of Science Editors:

Berthoumieux M. Étude pangénomique des sites de liaison de la protéine Rnt1p et de son rôle dans la maturation des snoARN chez Saccharomyces cerevisiae . [Masters Thesis]. Université de Sherbrooke; 2019. Available from: http://hdl.handle.net/11143/15200


University of Pennsylvania

29. Poplawski, Shane Gary. The Regulation of Gene Expression During Memory Consolidation in the Hippocampus.

Degree: 2014, University of Pennsylvania

 Memory consolidation is the process through which short-term memories are stabilized for long-term retention. New gene expression is required for this process to occur successfully.… (more)

Subjects/Keywords: ChIP-seq; Epigenetics; Gene Expression; Hippocampus; Memory; RNA-seq; Molecular Biology; Neuroscience and Neurobiology; Pharmacology

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Poplawski, S. G. (2014). The Regulation of Gene Expression During Memory Consolidation in the Hippocampus. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/1408

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Poplawski, Shane Gary. “The Regulation of Gene Expression During Memory Consolidation in the Hippocampus.” 2014. Thesis, University of Pennsylvania. Accessed May 22, 2019. https://repository.upenn.edu/edissertations/1408.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Poplawski, Shane Gary. “The Regulation of Gene Expression During Memory Consolidation in the Hippocampus.” 2014. Web. 22 May 2019.

Vancouver:

Poplawski SG. The Regulation of Gene Expression During Memory Consolidation in the Hippocampus. [Internet] [Thesis]. University of Pennsylvania; 2014. [cited 2019 May 22]. Available from: https://repository.upenn.edu/edissertations/1408.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Poplawski SG. The Regulation of Gene Expression During Memory Consolidation in the Hippocampus. [Thesis]. University of Pennsylvania; 2014. Available from: https://repository.upenn.edu/edissertations/1408

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

30. Bogeas, Alexandra. Méthylations de l'histone H3 et contrôle épigénétique des propriétés des cellules souches de gliomes : Histone H3 methylation and epigenetic control of glioma stem cells properties.

Degree: Docteur es, Neurosciences, 2013, Université Paris Descartes – Paris V

 Les gliomes sont les tumeurs primitives les plus fréquentes du cerveau et restent de mauvais pronostic en raison de l’inefficacité des traitements actuels. Des cellules… (more)

Subjects/Keywords: H3K4me3; H3K27me3; Cellules souches de gliomes; ChIP-seq; H3K4me3; H3K27me3; Glioma stem cells; ChIP-seq; 616.994 81

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APA (6th Edition):

Bogeas, A. (2013). Méthylations de l'histone H3 et contrôle épigénétique des propriétés des cellules souches de gliomes : Histone H3 methylation and epigenetic control of glioma stem cells properties. (Doctoral Dissertation). Université Paris Descartes – Paris V. Retrieved from http://www.theses.fr/2013PA05P620

Chicago Manual of Style (16th Edition):

Bogeas, Alexandra. “Méthylations de l'histone H3 et contrôle épigénétique des propriétés des cellules souches de gliomes : Histone H3 methylation and epigenetic control of glioma stem cells properties.” 2013. Doctoral Dissertation, Université Paris Descartes – Paris V. Accessed May 22, 2019. http://www.theses.fr/2013PA05P620.

MLA Handbook (7th Edition):

Bogeas, Alexandra. “Méthylations de l'histone H3 et contrôle épigénétique des propriétés des cellules souches de gliomes : Histone H3 methylation and epigenetic control of glioma stem cells properties.” 2013. Web. 22 May 2019.

Vancouver:

Bogeas A. Méthylations de l'histone H3 et contrôle épigénétique des propriétés des cellules souches de gliomes : Histone H3 methylation and epigenetic control of glioma stem cells properties. [Internet] [Doctoral dissertation]. Université Paris Descartes – Paris V; 2013. [cited 2019 May 22]. Available from: http://www.theses.fr/2013PA05P620.

Council of Science Editors:

Bogeas A. Méthylations de l'histone H3 et contrôle épigénétique des propriétés des cellules souches de gliomes : Histone H3 methylation and epigenetic control of glioma stem cells properties. [Doctoral Dissertation]. Université Paris Descartes – Paris V; 2013. Available from: http://www.theses.fr/2013PA05P620

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