The success of many clinical, association, or population genetics studies critically relies on properly performed variant calling step. The variety of modern genomics protocols, techniques, and platforms makes our choices of methods and algorithms difficult and there is no "one size fits all" solution for study design and data analysis. In this review, we discuss considerations that need to be taken into account while designing the study and preparing for the experiments. We outline the variety of variant types that can be detected using sequencing approaches and highlight some specific requirements and basic principles of their detection. Finally, we cover interesting developments that enable variant calling for a broad range of applicatio...
MotivationComputational methods are essential to extract actionable information from raw sequencing ...
A diversity of tools is available for identification of variants from genome sequence data. Given th...
Background: Reproducible detection of inherited variants with whole genome sequencing (WGS) is vital...
The success of many clinical, association, or population genetics studies critically relies on prope...
The success of many clinical, association, or population genetics studies critically relies on prope...
abstract: Analyzing human DNA sequence data allows researchers to identify variants associated with ...
The identification of genetic variants has great significance in genetic research. To call variants ...
Structural variants are generally defined as DNA variations larger than 50bp. They have been recogn...
To date, researchers and clinicians use widely different methods for detecting and reporting human g...
All human beings are approximately 99.9% similar in their DNA sequences. The 0.1% contains different...
Accurate and comprehensive variant discovery is extremely important for rare disease diagnostics us...
The development of short-read, next-generation sequencing (NGS) has revolutionized biological resear...
Rapid advancement of next-generation sequencing (NGS) technologies has facilitated the search for ge...
Abstract Background Sequencing studies of exonic regi...
Complete knowledge of the genetic variation in individual human genomes is a crucial foundation for ...
MotivationComputational methods are essential to extract actionable information from raw sequencing ...
A diversity of tools is available for identification of variants from genome sequence data. Given th...
Background: Reproducible detection of inherited variants with whole genome sequencing (WGS) is vital...
The success of many clinical, association, or population genetics studies critically relies on prope...
The success of many clinical, association, or population genetics studies critically relies on prope...
abstract: Analyzing human DNA sequence data allows researchers to identify variants associated with ...
The identification of genetic variants has great significance in genetic research. To call variants ...
Structural variants are generally defined as DNA variations larger than 50bp. They have been recogn...
To date, researchers and clinicians use widely different methods for detecting and reporting human g...
All human beings are approximately 99.9% similar in their DNA sequences. The 0.1% contains different...
Accurate and comprehensive variant discovery is extremely important for rare disease diagnostics us...
The development of short-read, next-generation sequencing (NGS) has revolutionized biological resear...
Rapid advancement of next-generation sequencing (NGS) technologies has facilitated the search for ge...
Abstract Background Sequencing studies of exonic regi...
Complete knowledge of the genetic variation in individual human genomes is a crucial foundation for ...
MotivationComputational methods are essential to extract actionable information from raw sequencing ...
A diversity of tools is available for identification of variants from genome sequence data. Given th...
Background: Reproducible detection of inherited variants with whole genome sequencing (WGS) is vital...