Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorder

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Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorder

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Bipolar affective disorder (BP) is a common, highly heritable psychiatric disorder characterized by periods of depression and mania. Using dense SNP genotype data, we characterized CNVs in 388 members of an Old Order Amish Pedigree with bipolar disorder. |

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Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorder

Bipolar affective disorder (BP) is a common, highly heritable psychiatric disorder characterized by periods of depression and mania. Using dense SNP genotype data, we characterized CNVs in 388 members of an Old Order Amish Pedigree with bipolar disorder. |

Gene copy number variation in natural populations of Plasmodium falciparum in Eastern Africa

Accuracy of analysis of cfDNA for detection of single nucleotide variants and copy number variants in breast cancer

GenomeCAT: A versatile tool for the analysis and integrative visualization of DNA copy number variants

Fast detection of de novo copy number variants from SNP arrays for case-parent trios

Concordance rate between copy number variants detected using either high- or medium-density single nucleotide polymorphism genotype panels and the potential of imputing copy number variants from flanking high density single nucleotide polymorphism haplotypes in cattle

Genetic variants in nuclear DNA along with environmental factors modify mitochondrial DNA copy number: A population-based exome-wide association study

Bayesian copy number detection and association in large-scale studies

Comparative study of whole exome sequencing-based copy number variation detection tools

DeviCNV: Detection and visualization of exon-level copy number variants in targeted next-generation sequencing data

Performance of copy number variants detection based on whole‑genome sequencing by DNBSEQ platforms

Đang chuẩn bị liên kết để tải về tài liệu: Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorder

Bipolar affective disorder (BP) is a common, highly heritable psychiatric disorder characterized by periods of depression and mania. Using dense SNP genotype data, we characterized CNVs in 388 members of an Old Order Amish Pedigree with bipolar disorder. |

Gene copy number variation in natural populations of Plasmodium falciparum in Eastern Africa

Accuracy of analysis of cfDNA for detection of single nucleotide variants and copy number variants in breast cancer

GenomeCAT: A versatile tool for the analysis and integrative visualization of DNA copy number variants

Fast detection of de novo copy number variants from SNP arrays for case-parent trios

Concordance rate between copy number variants detected using either high- or medium-density single nucleotide polymorphism genotype panels and the potential of imputing copy number variants from flanking high density single nucleotide polymorphism haplotypes in cattle

Genetic variants in nuclear DNA along with environmental factors modify mitochondrial DNA copy number: A population-based exome-wide association study

Bayesian copy number detection and association in large-scale studies

Comparative study of whole exome sequencing-based copy number variation detection tools

DeviCNV: Detection and visualization of exon-level copy number variants in targeted next-generation sequencing data

Performance of copy number variants detection based on whole‑genome sequencing by DNBSEQ platforms

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Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorder