<p>(A) <sup>classical</sup>CNVs are identified solely by variation among individuals in the copy number of genomic regions. (B) <i><sup>de nov</sup>°</i>CNVs are present in an individual but not in the soma of either of the parents. (C) <sup>cancer</sup>CNAs are copy number alterations that occur specifically in the cancer cells (orange) of an individual and, therefore, are absent from the healthy cells of the same individual (black). In this study we required <sup>cancer</sup>CNAs to be recurrent between individuals. (D) <sup>somatic</sup>CNVs are defined by regions that vary in copy number among the healthy somatic cells of an individual. (E) <sup>iPS</sup>CNVs are defined by regions that vary in copy number within a population of iPS cel...
Copy number variation (CNV) comprises a recently discovered kind of variation involving deletion and...
Item does not contain fulltextRecent studies have revealed a new type of variation in the human geno...
Genetic variation is the main reason of the phenotypic differences among individuals, as well as of ...
Copy number variants (CNVs) were the subject of extensive research in the past years. They are commo...
Recent studies have unveiled copy number variants (CNVs) as an important source of genetic variation...
Recent studies have unveiled copy number variants (CNVs) as an important source of genetic variation...
The extensive variability of individual human genomes contributes to phenotypic variability. Structu...
The extensive variability of individual human genomes contributes to phenotypic variability. Structu...
<p>(A) Boxplot showing the number of aberrant genes in deceased patients (right) and survivors (left...
DNA copy number variations (CNV) are common in cancer development, however, CNV detection approaches...
DNA copy number variations (CNV) are common in cancer development, however, CNV detection approaches...
Copy number variation (CNV) comprises a recently discovered kind of variation involving deletion and...
INDELs and CNVs are types of structural variations. This project aimed to computationally predict a...
Copy number variation (CNV) has recently gained considerable interest as a source of genetic variati...
Copy number Variants (CNVs), which comprise deletions, insertions and inversions of genomic sequence...
Copy number variation (CNV) comprises a recently discovered kind of variation involving deletion and...
Item does not contain fulltextRecent studies have revealed a new type of variation in the human geno...
Genetic variation is the main reason of the phenotypic differences among individuals, as well as of ...
Copy number variants (CNVs) were the subject of extensive research in the past years. They are commo...
Recent studies have unveiled copy number variants (CNVs) as an important source of genetic variation...
Recent studies have unveiled copy number variants (CNVs) as an important source of genetic variation...
The extensive variability of individual human genomes contributes to phenotypic variability. Structu...
The extensive variability of individual human genomes contributes to phenotypic variability. Structu...
<p>(A) Boxplot showing the number of aberrant genes in deceased patients (right) and survivors (left...
DNA copy number variations (CNV) are common in cancer development, however, CNV detection approaches...
DNA copy number variations (CNV) are common in cancer development, however, CNV detection approaches...
Copy number variation (CNV) comprises a recently discovered kind of variation involving deletion and...
INDELs and CNVs are types of structural variations. This project aimed to computationally predict a...
Copy number variation (CNV) has recently gained considerable interest as a source of genetic variati...
Copy number Variants (CNVs), which comprise deletions, insertions and inversions of genomic sequence...
Copy number variation (CNV) comprises a recently discovered kind of variation involving deletion and...
Item does not contain fulltextRecent studies have revealed a new type of variation in the human geno...
Genetic variation is the main reason of the phenotypic differences among individuals, as well as of ...