Portfolio

Allelic Variation Explorer (AVE)

A web-tool that allows visualization of single nucleotide polymorphisms (SNPs) by organizing them into haplotype blocks (here defined as a specific combination of nucleotides in a given stretch of DNA). AVE allows the exploration of very large resequencing projects (many resequenced accessions). AVE offers a wide range of functionality, such as counting the accessions in a haplotype block, exporting in fasta format, etc. Currently AVE is in production and to be implemented.

20 June, 2014

ELIXER FAIR and collaboration with DTL

In collaboration with DTL VLPB will act as one organization representing the interests of the VLPB members…

Galaxy

Based on the discussions and input from the VLBP associated companies…

GIBHUB

The Github environment was chosen and is used for development…

Snakemake framework

The de novo assembly, genome annotation, and variant calling pipeline…

Variant calling pipeline

A pipeline that takes NGS reads as input and which executes…

SNPCompare tool

Show a a cM or Mb based SNP density…

Allelic Variation Explorer (AVE)

A web-tool that allows visualization of single nucleotide polymorphisms (SNPs) by organizing…

White Paper Inventory NGS

An updatable inventory on technologies used in Next Generation Sequencing (NGS).

Redmine & Github VLPB Environment

An environment that contains all vlpb developed source code plus…

The VLPB Environment

Together with the VLPB Github environment a VLPB Google Group…

RNA run QC

A pipeline that takes NGS reads as input and produces a web page…

RNA counting pipeline

A pipeline for mapping and counting RNA seq reads including concentration spike-ins.

Size spike in visualization (small RNA-seq)

A visualization of counts of size spike-ins…

RNA experiment QC

A series of interactive visualizations using R-studio and a shiny-web server…

RNA normalization

A workflow to normalize RNA-seq experiments using spike-ins.