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