Whole-genome sequencing provides a rapid and powerful method for identifying mutations on a global scale, and has spurred a renewed enthusiasm for classical genetic screens in model organisms. The most commonly characterized category of mutation consists of monogenic, recessive traits, due to their genetic tractability. Therefore, most of the mapping methods for mutation identification by whole-genome sequencing are directed toward alleles that fulfill those criteria (i.e., single-gene, homozygous variants). However, such approaches are not entirely suitable for the characterization of a variety of more challenging mutations, such as dominant and semidominant alleles or multigenic traits. Therefore, we have developed strategies for the iden...
Background: A collection of genetic deficiencies covering over 70% of the Caenorhab...
Abstract Background: A collection of genetic deficiencies covering over 70% of the Caenorhabditis el...
Abstract Background Intragenic modifiers (in-phase, second-site variants) are known to have dramatic...
Whole-genome sequencing (WGS) is becoming a fast and cost-effective method to pinpoint molecular les...
Whole-genome sequencing is a powerful tool for analyzing genetic variation on a global scale. One pa...
Whole-genome sequencing (WGS) is an indispensable tool for identifying causal mutations obtained fro...
<div><p>Whole-genome sequencing is a powerful tool for analyzing genetic variation on a global scale...
Whole-genome sequencing represents a promising approach to pinpoint chemically induced mutations in ...
Single-nucleotide polymorphism (SNP) mapping is the easiest and most reliable way to map genes in Ca...
An essential requirement of genetic research is the ability to identify mutations. Forward genetic s...
Background: Essential genes are critical for the development of all organisms and are associated wit...
Genetic diversity is maintained by continuing generation and removal of variants. While examining ov...
Background: The original sequencing and annotation of the Caenorhabditis elegans ge...
Whole-genome sequencing represents a promising approach to pinpoint chemically induced mutations in ...
Genetic diversity is maintained by continuing generation and removal of variants. While examining ov...
Background: A collection of genetic deficiencies covering over 70% of the Caenorhab...
Abstract Background: A collection of genetic deficiencies covering over 70% of the Caenorhabditis el...
Abstract Background Intragenic modifiers (in-phase, second-site variants) are known to have dramatic...
Whole-genome sequencing (WGS) is becoming a fast and cost-effective method to pinpoint molecular les...
Whole-genome sequencing is a powerful tool for analyzing genetic variation on a global scale. One pa...
Whole-genome sequencing (WGS) is an indispensable tool for identifying causal mutations obtained fro...
<div><p>Whole-genome sequencing is a powerful tool for analyzing genetic variation on a global scale...
Whole-genome sequencing represents a promising approach to pinpoint chemically induced mutations in ...
Single-nucleotide polymorphism (SNP) mapping is the easiest and most reliable way to map genes in Ca...
An essential requirement of genetic research is the ability to identify mutations. Forward genetic s...
Background: Essential genes are critical for the development of all organisms and are associated wit...
Genetic diversity is maintained by continuing generation and removal of variants. While examining ov...
Background: The original sequencing and annotation of the Caenorhabditis elegans ge...
Whole-genome sequencing represents a promising approach to pinpoint chemically induced mutations in ...
Genetic diversity is maintained by continuing generation and removal of variants. While examining ov...
Background: A collection of genetic deficiencies covering over 70% of the Caenorhab...
Abstract Background: A collection of genetic deficiencies covering over 70% of the Caenorhabditis el...
Abstract Background Intragenic modifiers (in-phase, second-site variants) are known to have dramatic...