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Haplotyping

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Cover of 'Haplotyping'

Table of Contents

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    Book Overview
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    Chapter 1 Haplotyping of Heterozygous SNPs in Genomic DNA Using Long-Range PCR.
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    Chapter 2 Quantification and Sequencing of Crossover Recombinant Molecules from Arabidopsis Pollen DNA.
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    Chapter 3 PacBio for Haplotyping in Gene Families
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    Chapter 4 High Molecular Weight DNA Enrichment with Peptide Nucleic Acid Probes
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    Chapter 5 High-Throughput Sequencing of the Major Histocompatibility Complex following Targeted Sequence Capture
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    Chapter 6 Pedigree-Defined Haplotypes and Their Applications to Genetic Studies
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    Chapter 7 Haplotyping a Non-meiotic Diploid Fungal Pathogen Using Induced Aneuploidies and SNP/CGH Microarray Analysis.
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    Chapter 8 Whole-Genome Haplotyping of Single Sperm of Daphnia pulex (Crustacea, Anomopoda).
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    Chapter 9 Chromosome-Range Whole-Genome High-Throughput Experimental Haplotyping by Single-Chromosome Microdissection
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    Chapter 10 Phased Genome Sequencing Through Chromosome Sorting
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    Chapter 11 Long Fragment Read (LFR) Technology: Cost-Effective, High-Quality Genome-Wide Molecular Haplotyping
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    Chapter 12 Contiguity-Preserving Transposition Sequencing (CPT-Seq) for Genome-Wide Haplotyping, Assembly, and Single-Cell ATAC-Seq
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    Chapter 13 A Fosmid Pool-Based Next Generation Sequencing Approach to Haplotype-Resolve Whole Genomes
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    Chapter 14 Discovery of Rare Haplotypes by Typing Millions of Single-Molecules with Bead Emulsion Haplotyping (BEH)
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    Chapter 15 Computational Haplotype Inference from Pooled Samples
Attention for Chapter 9: Chromosome-Range Whole-Genome High-Throughput Experimental Haplotyping by Single-Chromosome Microdissection
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Chapter title
Chromosome-Range Whole-Genome High-Throughput Experimental Haplotyping by Single-Chromosome Microdissection
Chapter number 9
Book title
Haplotyping
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-6750-6_9
Pubmed ID
Book ISBNs
978-1-4939-6748-3, 978-1-4939-6750-6
Authors

Li Ma M.D., Ph.D., Wenzhi Li, Qing Song M.D., Ph.D., Li Ma, Qing Song

Editors

Irene Tiemann-Boege, Andrea Betancourt

Abstract

Haplotype is fundamental genetic information; it provides essential information for deciphering the functional and etiological roles of genetic variants. As haplotype information is closely related to the functional and etiological impact of genetic variants, it is widely anticipated that haplotype information will be extremely valuable in a wide spectra of applications, including academic research, clinical diagnosis of genetic disease and in the pharmaceutical industry. Haplotyping is essential for LD (linkage disequilibrium) mapping, functional studies on cis-interactions, big data imputation, association studies, population studies, and evolutionary studies. Unfortunately, current sequencing technologies and genotyping arrays do not routinely deliver this information for each individual, but yield only unphased genotypes. Here, we describe a high-throughput and cost-effective experimental protocol to obtain high-resolution chromosomal haplotypes of each individual diploid (including human) genome by the single-chromosome microdissection and sequencing approach.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 9 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 9 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 3 33%
Student > Bachelor 2 22%
Lecturer 1 11%
Researcher 1 11%
Professor > Associate Professor 1 11%
Other 0 0%
Unknown 1 11%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 4 44%
Agricultural and Biological Sciences 2 22%
Computer Science 1 11%
Decision Sciences 1 11%
Unknown 1 11%