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180208s2018 xxu| s |||| 0|eng d |
| 020 |
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|a 9781493974719
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| 024 |
7 |
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|a 10.1007/978-1-4939-7471-9
|2 doi
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| 040 |
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|a Sistema de Bibliotecas del Tecnológico de Costa Rica
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| 245 |
1 |
0 |
|a Disease Gene Identification :
|b Methods and Protocols /
|c edited by Johanna K. DiStefano.
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| 250 |
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|a 2nd ed. 2018.
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| 260 |
# |
# |
|a New York, NY :
|b Springer New York :
|b Imprint: Humana,
|c 2018.
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| 300 |
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|a X, 400 p. 63 illus., 50 illus. in color. :
|b online resource.
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| 336 |
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|a text
|b txt
|2 rdacontent
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| 337 |
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|a computer
|b c
|2 rdamedia
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| 338 |
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|a online resource
|b cr
|2 rdacarrier
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| 490 |
1 |
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|a Methods in Molecular Biology,
|v 1706
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| 505 |
0 |
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|a Identification of Disease Susceptibility Alleles in the Next Generation Sequencing Era -- Induced Pluripotent Stem Cells in Disease Modeling and Gene Identification -- Development of Targeted Therapies Based on Gene Modification -- What can we Learn about Human Disease from the Nematode C. elegans? -- Microbiome Sequencing Methods for Studying Human Diseases -- The Emerging Role of Long Noncoding RNAs in Human Disease -- Identification of Disease-related Genes using a Genome-wide Association Study Approach -- Whole Genome Library Construction for Next Generation Sequencing -- Whole Exome Library Construction for Next Generation Sequencing -- Optimized Methodology for the Generation of RNA-sequencing Libraries from Low-input Starting Material: Enabling Analysis of Specialized Cell Types and Clinical Samples -- Using C1 to Generate Single-cell Full-length cDNA Libraries for mRNA Sequencing -- MiSeq: A Next Generation Sequencing Platform for Genomic Analysis -- Methods for CpG Methylation Array Profiling via Bisulfite Conversion -- miRNA Quantification Method using Quantitative Polymerase Chain Reaction in Conjunction with the Cq Method -- Lentiviral--mediated CRISPR--cas9 Gene Editing of Primary Human Airway Epithelial Cells -- RNA Interference to Knockdown Gene Expression -- Using Luciferase Reporter Assays to Identify Functional Variants at Disease-associated Loci -- Physiologic Interpretation of GWAS Signals for type 2 Diabetes -- Identification of Genes for Hereditary Hemochromatosis -- Identification of Driver Mutations in Rare Cancers: The Role of SMARCA4 in Small Cell Carcinoma of the Ovary, Hypercalcemic Type (SCCOHT) -- The Rise and Fall and Rise of Linkage Analysis as a Technique for Finding and Characterizing Inherited Influences on Disease Expression.
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| 650 |
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0 |
|a Human genetics.
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| 650 |
1 |
4 |
|a Human Genetics.
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| 700 |
1 |
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|a DiStefano, Johanna K.
|e editor.
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| 710 |
2 |
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|a SpringerLink (Online service)
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| 773 |
0 |
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|t Springer eBooks
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| 900 |
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|a Libro descargado a ALEPH en bloque (proveniente de proveedor)
|