<div><p>With rapid decline of the sequencing cost, researchers today rush to embrace whole genome sequencing (WGS), or whole exome sequencing (WES) approach as the next powerful tool for relating genetic variants to human diseases and phenotypes. A fundamental step in analyzing WGS and WES data is mapping short sequencing reads back to the reference genome. This is an important issue because incorrectly mapped reads affect the downstream variant discovery, genotype calling and association analysis. Although many read mapping algorithms have been developed, the majority of them uses the universal reference genome and do not take sequence variants into consideration. Given that genetic variants are ubiquitous, it is highly desirable if they c...
Computational genomics involves the development and application of computational methods for whole-g...
Whole exome sequencing (WES) has been extensively used in genomic research. As sequencing costs decl...
Background: Reproducible detection of inherited variants with whole genome sequencing (WGS) is vital...
With rapid decline of the sequencing cost, researchers today rush to embrace whole genome sequencing...
With rapid decline of the sequencing cost, researchers today rush to embrace whole genome sequencing...
<p>(A) Comparison of genotype calling consistency among the five read mapping strategies for all chr...
Background: Typical human genome differs from the reference genome at 4-5 million sites. This divers...
The emergence of whole genome sequencing (WGS) has revolutionized the diagnosis of rare genetic diso...
The diploid nature of the human genome is neglected in many analyses done today, where a genome is p...
Copyright © 2014 Yanfeng Zhang et al.This is an open access article distributed under the Creative C...
Short read DNA sequencing technologies from Illumina have made sequencing a human genome significant...
Background: Accurate calling of SNPs and genotypes from next-generation sequencing data is an essent...
The human genome is diploid, which requires assigning heterozygous single nucleotide polymorphisms (...
With the completion of human genome sequencing project and the rapid development of sequencing techn...
BACKGROUND: The last two human genome assemblies have extended the previous linear golden-path parad...
Computational genomics involves the development and application of computational methods for whole-g...
Whole exome sequencing (WES) has been extensively used in genomic research. As sequencing costs decl...
Background: Reproducible detection of inherited variants with whole genome sequencing (WGS) is vital...
With rapid decline of the sequencing cost, researchers today rush to embrace whole genome sequencing...
With rapid decline of the sequencing cost, researchers today rush to embrace whole genome sequencing...
<p>(A) Comparison of genotype calling consistency among the five read mapping strategies for all chr...
Background: Typical human genome differs from the reference genome at 4-5 million sites. This divers...
The emergence of whole genome sequencing (WGS) has revolutionized the diagnosis of rare genetic diso...
The diploid nature of the human genome is neglected in many analyses done today, where a genome is p...
Copyright © 2014 Yanfeng Zhang et al.This is an open access article distributed under the Creative C...
Short read DNA sequencing technologies from Illumina have made sequencing a human genome significant...
Background: Accurate calling of SNPs and genotypes from next-generation sequencing data is an essent...
The human genome is diploid, which requires assigning heterozygous single nucleotide polymorphisms (...
With the completion of human genome sequencing project and the rapid development of sequencing techn...
BACKGROUND: The last two human genome assemblies have extended the previous linear golden-path parad...
Computational genomics involves the development and application of computational methods for whole-g...
Whole exome sequencing (WES) has been extensively used in genomic research. As sequencing costs decl...
Background: Reproducible detection of inherited variants with whole genome sequencing (WGS) is vital...