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Transcriptomics in Health and Disease

ISBN-13: 9783030878207 / Angielski / Twarda / 2022 / 488 str.

Transcriptomics in Health and Disease  9783030878207 Springer International Publishing - książkaWidoczna okładka, to zdjęcie poglądowe, a rzeczywista szata graficzna może różnić się od prezentowanej.

Transcriptomics in Health and Disease

ISBN-13: 9783030878207 / Angielski / Twarda / 2022 / 488 str.

cena 814,55
(netto: 775,76 VAT:  5%)

Najniższa cena z 30 dni: 771,08
Termin realizacji zamówienia:
ok. 16-18 dni roboczych.

Darmowa dostawa!

The study of transcriptomics is key to understanding complex diseases. This new edition will build on the foundation of the first edition while incorporating the progress that has been made in the field of transcriptomics in the past six years, including bioinformatics for data analysis. Written by leading experts, chapters address new subjects such as methodological advances in large-scale sequencing, the sequencing of single-cells, and spatial transcriptomics. The new edition will address how transcriptomics may be used in combination with genetic strategies to identify causative genes in monogenic and complex genetic diseases. Coverage will also explore transcriptomics in challenging groups of diseases, such as cancer, inflammation, bacterial infection, and autoimmune diseases. The updated volume will be useful for geneticists, genome biologists, biomedical researchers, molecular biologists, bioinformaticians, and students, among others.

Kategorie:
Nauka, Biologia i przyroda
Kategorie BISAC:
Medical > Genetyka kliniczna
Science > Life Sciences - Genetics & Genomics
Science > Biologia molekularna
Wydawca:
Springer International Publishing
Język:
Angielski
ISBN-13:
9783030878207
Rok wydania:
2022
Ilość stron:
488
Waga:
0.85 kg
Wymiary:
23.39 x 15.6 x 2.69
Oprawa:
Twarda
Wolumenów:
01
Dodatkowe informacje:
Wydanie ilustrowane

1. What is the transcriptome and how it is evaluated?.

2. ALTERNATIVE SPLICING OF PRE-MESSENGER RNA.

3. Transcriptome Analysis Using RNA-seq and scRNA-seq.

4. TRANSCRIPTOMICS OF NEONATAL AND INFANT HUMAN THYMUS.

5. Transcriptomics at the single cell level and human diseases: opportunities and challenges in data processing and analysis.

6. METHODS FOR GENE CO-EXPRESSION NETWORK VISUALIZATION AND ANALYSIS.

7. Comparative Analysis of Packages and Algorithms for the Analysis of Spatially Resolved Transcriptomics Data.

8. The Interplay Between the Transcriptomics and Proteomics Profiles.

9. TRANSCRIPTOME DURING NORMAL CELL DIFFERENTIATION.

10. Transcriptomics to dissect the Immune System.

11. Transcriptome Profiling in Autoimmune Diseases.

12. Transcriptome Profiling in Experimental Inflammatory Arthritis.

13. TRANSCRIPTOMICS AND IMMUNE RESPONSE IN HUMAN CANCER.

14. MicroRNAs in Cancer.

15. Oxidative Stress, DNA Damage and Transcriptional Expression of DNA Repair and Stress Response Genes in Diabetes Mellitus.

16. Large-scale gene expression in monogenic and complex genetic diseases.

17. Transcriptome in Human Mycoses.

18. Understanding Chagas Disease by Multi-omics data Integration, Functional and Enrichment Computational Analysis.

Geraldo Aleixo Passos received his PhD degree in biochemistry (1988) from Ribeirão Preto Medical School, University of São Paulo, USP, Brazil. His postdoctoral studies were conducted at the Molecular Genetics Institute of Montpellier (CNRS), France (1992-94) with sequencing and physical mapping of the human immunoglobulin lambda locus on chromosome 22q11.2. For several years, he worked in close collaboration with the microarray laboratory at Centre d´Immunologie de Marseille-Luminy (CIML, Marseille, France) (1999-2001) and then the Unité INSERM 1090 in Marseille (2002-17) to study the large-scale gene expression in the thymus.  He is currently Associate Professor (Genetics and Molecular Biology) at School of Dentistry and Ribeirão Preto Medical School (USP, Campus of Ribeirão Preto, Brazil) in which he is the coordinator of the Molecular Immunogenetics Group.

The study of transcriptomics is key to understanding complex diseases. This new edition will build on the foundation of the first edition while incorporating the progress that has been made in the field of transcriptomics in the past six years, including bioinformatics for data analysis. Written by leading experts, chapters address new subjects such as methodological advances in large-scale sequencing, the sequencing of single-cells, and spatial transcriptomics. The new edition will address how transcriptomics may be used in combination with genetic strategies to identify causative genes in monogenic and complex genetic diseases. Coverage will also explore transcriptomics in challenging groups of diseases, such as cancer, inflammation, bacterial infection, and autoimmune diseases. The updated volume will be useful for geneticists, genome biologists, biomedical researchers, molecular biologists, bioinformaticians, and students, among others.



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