Search Results - "DNA sequencing"
Suggested Topics within your search.
Suggested Topics within your search.
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1
Genome sequencing technology and algorithms
Published 2008Table of Contents: “…An overview of new DNA sequencing technology -- Array-based pyrosequencing technology -- The role of resequencing arrays in revolutionizing DNA sequencing -- Polony sequencing -- Genome sequencing: a complex path to personalized medicine -- Overview of genome assembly techniques -- Fragment assembly algorithms -- Assembly for double-ended short read sequencing technologies -- Genome characterization in the post-human genome project era -- The haplotyping problem: an overview of computational models and solutions -- Analysis of genomic alterations in cancer -- High-throughput assessments of epigenomics in human disease -- Comparative sequencing, assembly, and anchoring.…”
NetLibrary
Electronic eBook -
2
DNA promise and peril /
Published 2008Table of Contents: “…DNA sequence does not equal destiny -- What is genomics? …”
NetLibrary
Electronic eBook -
3
Medical sciences at a glance
Published 2014Table of Contents: “…Metabolism of the remaining carbon skeletonsAminoacidopathies -- Part 3: Molecular and medical genetics; 14: Principles of molecular genetics; Gene cloning; Libraries; Isolation of a specific DNA sequence; DNA sequencing; Practical applications; Gene mapping; Protein synthesis; Prenatal diagnosis of disease; 15: DNA and RNA; Deoxyribonucleic acid (DNA); DNA sequence; The DNA double helix; DNA organisation in human cells; DNA replication; Ribonucleic acid (RNA); 16: Gene expression; Transcription (Figure 16.1); Control of transcription; Translation; The genetic code; 17: Medical genetics. …”
Book -
4
Clinical genomics a guide to clinical next generation sequencing
Published 2015Table of Contents: “…Nikiforov -- Emerging DNA sequencing technologies / Shashikant Kulkarni and John Pfeifer -- RNA-sequencing and methylome analysis / Shamika Ketkar and Shashikant Kulkarni -- Base calling, read mapping, and coverage analysis / Paul Cliften -- Single nucleotide variant detection using next generation sequencing / David H. …”
Book


