Conecte-se

Bibliografias temáticas / High throughput sequencing (NGS) / Livros

Livros sobre o tema "High throughput sequencing (NGS)"

Siga este link para ver outros tipos de publicações sobre o tema: High throughput sequencing (NGS).

Autor: Grafiati

Publicado: 27 de julho de 2024

Última modificação: 29 de julho de 2024

Crie uma referência precisa em APA, MLA, Chicago, Harvard, e outros estilos

Selecione um tipo de fonte:

Veja os 50 melhores livros para estudos sobre o assunto "High throughput sequencing (NGS)".

Ao lado de cada fonte na lista de referências, há um botão "Adicionar à bibliografia". Clique e geraremos automaticamente a citação bibliográfica do trabalho escolhido no estilo de citação de que você precisa: APA, MLA, Harvard, Chicago, Vancouver, etc.

Você também pode baixar o texto completo da publicação científica em formato .pdf e ler o resumo do trabalho online se estiver presente nos metadados.

Veja os livros das mais diversas áreas científicas e compile uma bibliografia correta.

1

Kwon, Young Min, e Steven C. Ricke, eds. High-Throughput Next Generation Sequencing. Totowa, NJ: Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-089-8.

Texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

2

Rodríguez-Ezpeleta, Naiara, Michael Hackenberg e Ana M. Aransay, eds. Bioinformatics for High Throughput Sequencing. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-0782-9.

Texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

3

Rodríguez-Ezpeleta, Naiara, Michael Hackenberg e Ana M. Aransay. Bioinformatics for high throughput sequencing. New York, NY: Springer, 2012.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

4

R, Mitchelson Keith, ed. New high throughput technologies for DNA sequencing and genomics. Amsterdam: Elsevier, 2007.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

5

Aransay, Ana M., e José Luis Lavín Trueba, eds. Field Guidelines for Genetic Experimental Designs in High-Throughput Sequencing. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-31350-4.

Texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

6

author, Belazzougui Djamal, Cunial Fabio author e Tomescu Alexandru I. author, eds. Genome-scale algorithm design: Biological sequence analysis in the era of high-throughput sequencing. Cambridge, United Kingdom: University Printing House, 2015.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

7

Cunha, Monica V., e João Inácio. Veterinary infection biology: Molecular diagnostics and high-throughput strategies. New York: Humana Press, 2015.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

8

Rodríguez-Ezpeleta, Naiara, Ana M. Aransay e Michael Hackenberg. Bioinformatics for High Throughput Sequencing. Springer, 2014.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

9

Rodríguez-Ezpeleta, Naiara, Ana M. Aransay e Michael Hackenberg. Bioinformatics for High Throughput Sequencing. Springer, 2011.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

10

Lee, Eric, e T. W. Tan. Beginners Guide to Bioinformatics for High Throughput Sequencing. WORLD SCIENTIFIC, 2018. http://dx.doi.org/10.1142/10720.

Texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

11

High-throughput next generation sequencing: Methods and applications. New York: Springer, 2011.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

12

Tan, Hugh T. W., e Eric Lee. Beginners Guide to Bioinformatics for High Throughput Sequencing. World Scientific Publishing Co Pte Ltd, 2018.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

13

Kwon, Young Min, e Steven C. Ricke. High-Throughput Next Generation Sequencing: Methods and Applications. Humana Press, 2016.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

14

Beginners Guide to Bioinformatics for High Throughput Sequencing. World Scientific Publishing Co Pte Ltd, 2018.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

15

Ball, Madeleine Price. Sequencing-based high-throughput profiling of DNA methylation. 2010.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

16

New High Throughput Technologies for DNA Sequencing and Genomics. Elsevier, 2007. http://dx.doi.org/10.1016/s1871-0069(06)x0200-8.

Texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

17

Joly, Dominique, e Denis Faure. Insight on Environmental Genomics: The High-Throughput Sequencing Revolution. Elsevier, 2016.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

18

Joly, Dominique, e Denis Faure. Insight on Environmental Genomics: The High-Throughput Sequencing Revolution. Elsevier, 2016.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

19

Mitchelson, Keith R. New High Throughput Technologies for DNA Sequencing and Genomics. Elsevier Science & Technology Books, 2011.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

20

Aransay, Ana M., e José Luis Lavín Trueba. Field Guidelines for Genetic Experimental Designs in High-Throughput Sequencing. Springer London, Limited, 2016.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

21

Aransay, Ana M., e José Luis Lavín Trueba. Field Guidelines for Genetic Experimental Designs in High-Throughput Sequencing. Springer, 2016.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

22

Aransay, Ana M., e José Luis Lavín Trueba. Field Guidelines for Genetic Experimental Designs in High-Throughput Sequencing. Springer, 2018.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

23

Li, Hua, Wen-Lian Chen, Yuriy L. Orlov e Guoshuai Cai, eds. High-throughput Sequencing-based Investigation of Chronic Disease Markers and Mechanisms. Frontiers Media SA, 2022. http://dx.doi.org/10.3389/978-2-88976-559-1.

Texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

24

In Loeffler’s Footsteps – Viral Genomics in the Era of High-Throughput Sequencing. Elsevier, 2017. http://dx.doi.org/10.1016/s0065-3527(17)x0003-1.

Texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

25

Genome-Scale Algorithm Design: Bioinformatics in the Era of High-Throughput Sequencing. Cambridge University Press, 2023.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

26

Beer, Martin, e Dirk Höper. In Loeffler's Footsteps: Viral Genomics in the Era of High-Throughput Sequencing. Elsevier Science & Technology Books, 2017.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

27

Beer, Martin, e Dirk Höper. In Loeffler's Footsteps - Viral Genomics in the Era of High-Throughput Sequencing. Elsevier Science & Technology Books, 2017.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

28

Next-generation sequencing : current technologies and applications. Caister Academic Press, 2014.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

29

Tomescu, Alexandru I., Veli Mäkinen, Djamal Belazzougui e Fabio Cunial. Genome-Scale Algorithm Design: Biological Sequence Analysis in the Era of High-Throughput Sequencing. Cambridge University Press, 2015.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

30

Tomescu, Alexandru I., Veli Mäkinen, Djamal Belazzougui e Fabio Cunial. Genome-Scale Algorithm Design: Biological Sequence Analysis in the Era of High-Throughput Sequencing. Cambridge University Press, 2015.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

31

DeKosky, Brandon. Decoding the Antibody Repertoire: High Throughput Sequencing of Multiple Transcripts from Single B Cells. Springer, 2018.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

32

DeKosky, Brandon. Decoding the Antibody Repertoire: High Throughput Sequencing of Multiple Transcripts from Single B Cells. Springer International Publishing AG, 2017.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

33

Genome-Scale Algorithm Design: Biological Sequence Analysis in the Era of High-Throughput Sequencing. Cambridge University Press, 2023.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

34

Shomron, Noam. Deep Sequencing Data Analysis. Springer, 2022.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

35

Shomron, Noam. Deep Sequencing Data Analysis. Humana Press, 2016.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

36

Shomron, Noam. Deep Sequencing Data Analysis. Springer, 2020.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

37

Deep Sequencing Data Analysis. Humana Press Inc., 2013.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

38

Chandran, Anandhakumar. Advancing Development of Synthetic Gene Regulators: With the Power of High-Throughput Sequencing in Chemical Biology. Springer, 2017.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

39

Chandran, Anandhakumar. Advancing Development of Synthetic Gene Regulators: With the Power of High-Throughput Sequencing in Chemical Biology. Springer, 2017.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

40

Chandran, Anandhakumar. Advancing Development of Synthetic Gene Regulators: With the Power of High-Throughput Sequencing in Chemical Biology. Springer, 2019.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

41

Mitchelson, Keith. New High Throughput Technologies for DNA Sequencing and Genomics, Volume 2 (Perspectives in Bioanalysis) (Perspectives in Bioanalysis). Elsevier Science, 2007.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

42

Applications Of Next Generation Sequencing In Cancer Research Vol 1 Decoding The Cancer Genome. Springer-Verlag New York Inc., 2013.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

43

Mifsud, Borbala, e Anais Bardet. Practical Guide to Chip-Seq Data Analysis. Taylor & Francis Group, 2018.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

44

Mifsud, Borbala, Kathi Zarnack e Anaïs F. Bardet. Practical Guide to ChIP-Seq Data Analysis. Taylor & Francis Group, 2018.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

45

Mifsud, Borbala, Kathi Zarnack e Anais Bardet. Practical Guide to Chip-Seq Data Analysis. Taylor & Francis Group, 2021.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

46

Mifsud, Borbala, Kathi Zarnack e Anaïs F. Bardet. Practical Guide to ChIP-Seq Data Analysis. Taylor & Francis Group, 2018.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

47

Practical Guide to ChIP-Seq Data Analysis. Taylor & Francis Group, 2018.

Encontre o texto completo da fonte

Estilos ABNT, Harvard, Vancouver, APA, etc.

48

Lamari, Foudil, e Jean-Marie Saudubray. Disorders of Complex Lipids Synthesis and Remodeling. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199972135.003.0066.

Texto completo da fonte

Resumo:

Defective lipid catabolic pathways are involved in numerous inherited metabolic diseases such as lysosomal storage diseases and peroxisome biogenesis disorders. We recently described a new classification of a rapidly growing group of inherited metabolic disorders involving biosynthesis and remodeling of complex lipids including phospholipids and sphingolipids. The remarkable progress achieved over the last decade in high throughput gene sequencing and in lipid analysis technologies have enabled the description of more than 40 diseases linked to defects in enzymes involved in these pathways. Some of these defects present in infancy or childhood but most of them are diagnosed in adolescence or adulthood. In this review we focus on those with adult presentation.

Estilos ABNT, Harvard, Vancouver, APA, etc.

49

Ayala, Francisco J., e Camilo J. Cela-Conde. Neanderthals and modern humans. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780198739906.003.0011.

Texto completo da fonte

Resumo:

This chapter deals with the similarities and differences between Homo neanderthalensis and Homo sapiens, by considering genetic, brain, and cognitive evidence. The genetic differentiation emerges from fossil genetic evidence obtained first from mtDNA and later from nuclear DNA. With high throughput whole genome sequencing, sequences have been obtained from the Denisova Cave (Siberia) fossils. Nuclear DNA of a third species (“Denisovans”) has been obtained from the same cave and used to define the phylogenetic relationships among the three species during the Upper Palaeolithic. Archaeological comparisons make it possible to advance a four-mode model of the evolution of symbolism. Neanderthals and modern humans would share a “modern mind” as defined up to Symbolic Mode 3. Whether the Neanderthals reached symbolic Mode 4 remains unsettled.

Estilos ABNT, Harvard, Vancouver, APA, etc.

50

Haiman, Christopher, e David J. Hunter. Genetic Epidemiology of Cancer. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780190676827.003.0004.

Texto completo da fonte

Resumo:

This chapter explores the genetic epidemiology of cancer: the identification and quantification of inherited genetic factors, and their potential interaction with the environment, in the etiology of cancer in human populations. It also describes the techniques used to identify genetic variants that contribute to cancer susceptibility. It describes the older research methods for identifying the chromosomal localization of high-risk predisposing genes, such as linkage analysis within pedigrees and allele-sharing methods, as it is important to understand the foundations of the field. It also reviews the epidemiologic study designs that can be helpful in identifying low-risk alleles in candidate gene and genome-wide association studies, as well as gene–environment interactions. Finally, it describes some of the genotyping and sequencing platforms commonly employed for high-throughput genome analysis, and the concept of Mendelian randomization and how it may be useful in the study of biomarkers and environmental causes of cancer.

Estilos ABNT, Harvard, Vancouver, APA, etc.

Oferecemos descontos em todos os planos premium para autores cujas obras estão incluídas em seleções literárias temáticas. Contate-nos para obter um código promocional único!