Titel: | Disease gene identification |
Titelzusatz: | methods and protocols |
Mitwirkende: | DiStefano, Johanna K. [HerausgeberIn] |
Verf.angabe: | edited by Johanna K. DiStefano |
Ausgabe: | Second edition |
Verlagsort: | New York, NY |
Verlag: | Humana Press |
E-Jahr: | 2018 |
Jahr: | [2018] |
Umfang: | x, 400 Seiten |
Illustrationen: | Illustrationen |
Format: | 25.4 cm x 17.8 cm |
Gesamttitel/Reihe: | Methods in molecular biology ; 1706 |
| Springer protocols |
Ang. zum Inhalt: | Identification of disease susceptibility alleles in the next generation sequencing era / Johanna K. DiStefano and Christopher B. Kingsley |
| Induced pluripotent stem cells in disease modeling and gene identification / Satish Kumar, John Blangero, and Joanne E. Curran |
| Development of targeted therapies based on gene modification / Taylor M. Benson, Fatjon Leti, and Johanna K. DiStefano |
| What can we learn about human disease from the nematode C. elegans / Javier Apfeld and Scott Alper |
| Microbiome sequencing methods for studying human diseases / Rebecca M. Davidson and L. Elaine Epperson |
| Emerging role of long noncoding RNAs in human disease / Johanna K. DiStefano |
| Identification of disease-related genes using a genome-wide association study approach / Tobias Wohland and Dorit Schleinitz |
| Whole genome library construction for next generation sequencing / Jonathan J. Keats, Lori Cuyugan, Jonathan Adkins, and Winnie S. Liang |
| Whole exome library construction for next generation sequencing / Winnie S. Liang, Kristi Stephenson, Jonathan Adkins, Austin Christofferson, Adrienne Helland, Lori Cuyugan, and Jonathan J. Keats |
| Optimized methodology for the generation of RNA-sequencing libraries from low-input starting material : enabling analysis of specialized cell types and clinical samples / Kendra Walton and Brian P. O'Connor |
| Using fluidigm C1 to generate single-cell full-length cDNA libraries for mRNA sequencing / Robert Durruthy-Durruthy and Manisha Ray |
| MiSeq : a next generation sequencing platform for genomic analysis / Rupesh Kanchi Ravi, Kendra Walton, and Mahdieh Khosroheidari |
| Methods for CpG methylation array profiling via bisulfite conversion / Fatjon Leti, Lorida Llaci, Ivana Malenica, and Johanna K. DiStefano |
| miRNA quantification method using quantitative polymerase chain reaction in conjunction with Cq method / Fatjon Leti and Johanna K. DiStefano |
| Primary airway epithelial cell gene editing using CRISPR-Cas9 / Jamie L. Everman, Cydney Rios, and Max A. Seibold |
| RNA interference to knock down gene expression / Haiyong Han |
| Using luciferase reporter assays to identify functional variants at disease-associated loci / Anup K. Nair and Leslie J. Baier |
| Physiologic interpretation of GWAS signals for type 2 diabetes / Richard M. Watanabe |
| Identification of Genes for Hereditary Hemochromatosis / Glenn S. Gerhard, Barbara V. Paynton, and Johanna K. DiStefano |
| Identification of driver mutations in rare cancers : the role of SMARCA4 in small cell carcinoma of the ovary, hypercalcemic type (SCCOHT) / Jessica D. Lang and William P.D. Hendricks |
| Rise and fall and rise of linkage analysis as a technique for finding and characterizing inherited influences on disease expression / Ettie M. Lipner and David A. Greenberg. |
ISBN: | 978-1-4939-7470-2 |
| 978-1-4939-7471-9 |
| 1-4939-7470-X |
Bestellnr.: | 978-1-4939-7470-2 |
| 86873344 |
URL: | Inhaltsverzeichnis: http://digitale-objekte.hbz-nrw.de/storage2/2018/03/14/file_40/7596934.pdf |
Schlagwörter: | (s)Krankheit / (s)Genanalyse |
| (s)Krankheit / (s)Genanalyse |
Dokumenttyp: | Aufsatzsammlung |
Sprache: | eng |
RVK-Notation: | WG 9000 |
K10plus-PPN: | 1018519572 |
Verknüpfungen: | → Übergeordnete Aufnahme |
Disease gene identification / DiStefano, Johanna K. [HerausgeberIn]; [2018]