High throughput sequencing is generating large datasets that can be used provide important insights into genomic variation and biology. There is a need to visualize single nucleotide polymorphisms, insertions and deletions, and other structural variants from new sequence file formats. We have developed VarB software that can read in multi-sample VCF files, and visualize and critically assess contents and identify informative markers to discriminate between user-defined groups
The study of such a complex phenomenon as cancer, which depends on several but unexplored and unclea...
This file is the set of single nucleotide polymorphisms and insertion/deletions in a population of D...
Background. Most genetic disorders are caused by single nucleotide variations (SNVs) or small insert...
SUMMARY: There is an immediate need for tools to both analyse and visualize in real-time single-nucl...
Since its introduction in 2011 the variant call format (VCF) has been widely adopted for processing ...
Background. High-throughput sequencing platforms generate a massive amount of high-dimensional genom...
Following variant calling and annotation, accurate variant filtering is a crucial step to extract me...
Next-generation sequencing technologies have become the most powerful tool to discover genetic varia...
International audienceWith the rapidly developing high-throughput sequencing technologies known as n...
Introduction: High-throughput sequencing platforms generate a massive amount of high-dimensional ge...
Summary: The Variant Call Format (VCF) is a generic format for storing DNA polymorphism data such as...
SUMMARY: The variant call format (VCF) is a generic format for storing DNA polymorphism data such as...
This is the final cleaned and filtered VCF file used for downstream population genetic and landscape...
Background: Since the advent of next-generation sequencing many previously untestable hypotheses hav...
Compressed vcf (variant call format) file containing the genetic data for the 206,047 single nucleot...
The study of such a complex phenomenon as cancer, which depends on several but unexplored and unclea...
This file is the set of single nucleotide polymorphisms and insertion/deletions in a population of D...
Background. Most genetic disorders are caused by single nucleotide variations (SNVs) or small insert...
SUMMARY: There is an immediate need for tools to both analyse and visualize in real-time single-nucl...
Since its introduction in 2011 the variant call format (VCF) has been widely adopted for processing ...
Background. High-throughput sequencing platforms generate a massive amount of high-dimensional genom...
Following variant calling and annotation, accurate variant filtering is a crucial step to extract me...
Next-generation sequencing technologies have become the most powerful tool to discover genetic varia...
International audienceWith the rapidly developing high-throughput sequencing technologies known as n...
Introduction: High-throughput sequencing platforms generate a massive amount of high-dimensional ge...
Summary: The Variant Call Format (VCF) is a generic format for storing DNA polymorphism data such as...
SUMMARY: The variant call format (VCF) is a generic format for storing DNA polymorphism data such as...
This is the final cleaned and filtered VCF file used for downstream population genetic and landscape...
Background: Since the advent of next-generation sequencing many previously untestable hypotheses hav...
Compressed vcf (variant call format) file containing the genetic data for the 206,047 single nucleot...
The study of such a complex phenomenon as cancer, which depends on several but unexplored and unclea...
This file is the set of single nucleotide polymorphisms and insertion/deletions in a population of D...
Background. Most genetic disorders are caused by single nucleotide variations (SNVs) or small insert...
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